US3274213A - Alkoxy-substituted 2-phenyl-1-(tertiary-aminoalkoxy)phenyl-3, 4-dihydronaphthalenes - Google Patents

Alkoxy-substituted 2-phenyl-1-(tertiary-aminoalkoxy)phenyl-3, 4-dihydronaphthalenes Download PDF

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US3274213A
US3274213A US296939A US29693963A US3274213A US 3274213 A US3274213 A US 3274213A US 296939 A US296939 A US 296939A US 29693963 A US29693963 A US 29693963A US 3274213 A US3274213 A US 3274213A
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bromobenzene
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Lednicer Daniel
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Pharmacia and Upjohn Co
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
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    • A61K31/135Amines having aromatic rings, e.g. ketamine, nortriptyline
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/45Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
    • C07C45/46Friedel-Crafts reactions
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/753Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups
    • C07C49/755Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups a keto group being part of a condensed ring system with two or three rings, at least one ring being a six-membered aromatic ring
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    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/58Unsaturated compounds containing ether groups, groups, groups, or groups
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
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    • C07C65/00Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C65/21Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms

Definitions

  • This invention relates to novel 3,4-dihydronaphthalenes and is more particularly concerned with novel alkoxy substituted 2-phenyl-l-(tertiaryaminoalkoxy) phenyl-3,4-dihydronaphthalenes and acid addition salts, quaternary ammonium salts, N-oxides and N-oxide acid addition salts thereof, and with processes for their preparation.
  • novel compounds of the invention are selected from the class consisting of (a) the free bases, (b) the pharmacologically acceptable acid addition salts, (c) the N-oxides, (d) the N-oxide pharmacologically acceptable acid addition salts, and (e) the quaternary ammonium salts of compounds having the formula:
  • R and R are selected from the class consisting of lower-alkyl and lower-alkyl linked together to form a 5 to 7 ring atom saturated heterocyclic radical, one of the ring atoms of which, in addition to the amino nitrogen atom, is selected from the class consisting of carbon nitrogen, and oxygen, the other ring atoms being carbon,
  • C H represents alkylene from 2 to 6 carbon atoms, inclusive
  • alkoxy contains from 1 to 8 carbon atoms, inclusive
  • x is an integer from 1 to 4, inclusive.
  • lower-alkyl means an alkyl group containing from 1 to 8 carbon atoms, inclusive, such as methyl, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, and isomeric forms thereof.
  • alkoxy containing from 1 to 8 carbon atoms, inclusive are methoxy, ethoxy, propoxy, butoxy, amyloxy, hexyloxy, heptyloxy, octyloxy, and isomeric forms thereof.
  • lower alkyl groups linked together to form a 5 to 7 ring atom saturated heterocyclic radical one of the ring atoms of which, in addition to the amino nitrogen atom, is selected from the class consisting of carbon, nitrogen, and oxygen, the other ring atoms being carbon is inclusive pyrrolidino, Z-methylpyrrolidino, 2,2- dimethylpyrrolidino, and like alkylpyrrolidino groups, piperazino, 4-methylpiperazino, 2,4-dimethylpiperazino, and like alkylpiperazino groups, morpholino, piperidino, Z-methylpiperidino, 3-methylpiperidino, and like alkylpiperidino groups, hexamethyleneimino, homopiperazino, homomorpholino, and the like.
  • the acid addition salts of the invention comprise the salts of the compounds having the Formula I and of the "ice corresponding N-oxides with pharmacologically acceptable acids such as sulfuric, hydrochloric, nitric, phosphoric, lactic, benzoic, methane-sulfonic, p-toluenesulfonic, salicylic, acetic, propionic, maleic, malic, tartaric, citric, cyclohexylsulfamic, succinic, nicotinic, ascorbic acids, and the like.
  • pharmacologically acceptable acids such as sulfuric, hydrochloric, nitric, phosphoric, lactic, benzoic, methane-sulfonic, p-toluenesulfonic, salicylic, acetic, propionic, maleic, malic, tartaric, citric, cyclohexylsulfamic, succinic, nicotinic, ascorbic
  • the quaternary ammonium salts of the invention are the salts obtained by reacting the free bases having the Formula I with quaternating agents, for example, lower alkyl halides, lower-alkenyl halides, di(lower-alkyl) sulfates, aralkyl halides, lower-alkyl arylsulfonates, and the like.
  • quaternating agents for example, lower alkyl halides, lower-alkenyl halides, di(lower-alkyl) sulfates, aralkyl halides, lower-alkyl arylsulfonates, and the like.
  • lower-alkyl has the meaning hereinbefore defined.
  • aralkyl means an aralkyl group containing from 7 to 13 carbon atoms, inclusive, such as benzyl, phenethyl, phenylpropyl, benzhydryl, and the like.
  • Examples of quaternary salts of the compounds of Formula I are the methobromide, methiodide, ethobromide, propyl chloride, butyl bromide, octyl bromide, methyl methosulfate, ethyl ethosulfate, allyl chloride, allyl bromide, benzyl bromide, benzhydryl chloride, methyl toluenesulfonate, and the like.
  • novel compounds of the invention including the free bases of Formula I, the acid addition salts thereof, the quaternary ammonium salts thereof, and the corresponding N-oxides and N-oxide acid addition salts possess pharmacological activity.
  • the compounds of the invention are useful as anti-inflammatory agents, antifertility agents, antiestrogenic agents, and as agents for the lowering of cholesterol blood levels in mammals including man and animals of economic value.
  • novel compounds of the invention can be employed per se, for example, enclosed in a hard capsule for oral administration, or can be combined with solid or liquid pharmaceutical carriers and formulated in the form of tablets, powder packets, or capsules, using starch and like excipients, or dissolved or suspended in suitable solvents or vehicles, for oral or parenteral administration.
  • the compounds of the invention are also useful as intermediates.
  • the compounds having the Formula I can be reacted with fiuosilicic acid to form the fluosilicate salts which in dilute aqueous solution are effective mothproofing agents as more fully disclosed in US. Patents 2,075,359 and 1,915,334.
  • novel compounds of the invention having the Formula I can be prepared by reaction of an appropriately substituted l-keto-1,2,3,4-tetrahydronaphthalene (i.e., an a-tetralone) having the formula:
  • Suitable inert solvents include diisopropyl ether, diisobutyl ether, tetrahydrofuran, and the like.
  • the reaction can be carried out at temperatures within the range of about C. to about the boiling point of the solvent employed and is preferably carried out at elevated temperatures, for example, at or near the boiling point of the reaction mixture.
  • reaction time varies within wide limits according to the temperature at which the reaction is conducted. Generally speaking, where the reaction is carried out at elevated temperatures such as the boiling point of the reaction mixture, it is necessary to employ a reaction time of the order of several hours to ensure completion of the reaction.
  • the desired dihydron-aphthaleue having the Formula I can be isolated from the reaction mixture by conventional procedures, for example, by decomposing the reaction mixture with water, ammonium chloride, and the like, followed by separation of the organic layer and removal of solvent therefrom.
  • the product so obtained is largely the desired compound (I) contaminated with minor impurities and unchanged starting material which can be removed by simple procedures, for example by isolation of the desired compound (I) as an acid addition salt.
  • the compound (IV) when obtained as the major reaction product or when present in significant quantities in the above-described reaction product, can be converted to the desired compound (I) by dehydration.
  • the dehydration can be effected in most instances by heating the compound (IV) in a solvent such as benzene, toluene, xylene, and the like which forms an azeotrope with water, in the presence of a trace of a strong acid such as hydrochloric, sulfuric, p-toluenesulforn'c acids and the like.
  • the water which is formed in the dehydration is removed from the reaction mixture azeotropically. There is thereby obtained a solution of the desired compound (I) from which the latter can be isolated by evaporation or other conventional procedures.
  • the dehydration of the l-hydroxy-l,2, 3,4-tetrahydronaphthalene (IV) requires more drastic conditions such as heating the compound at, or slightly above, its melting point, preferably in the presence of an inert gas, until evolution of water is complete.
  • the Grignard reagents having the Formula III which are employed as starting materials in the process of the invention can be prepared by reaction of magnesium in an anhydrous inert organic solvent such as diisopropyl ether,
  • R R C H and Hal have the significance hereinbefore defined, using procedures well-known in the art for the preparation of Grignard reagents.
  • the halobenzenes having the Formula V can be prepared by etherification of the corresponding halophenol with the appropriate tertiaryaminoalkyl halide N CnH2n-Ha1 R2 wherein R R and C H and Hal have the significance hereinbefore defined.
  • the etherification is conducted advantage'ously in an inert solvent such as a lower alkanol,
  • the condensation between the secondary amine NH R2 and the haloalkanol Hal-C H OH can be carried out. for example, using the procedure described by Moffett. J. Org. Chem. 14, 862, 1949.
  • the desired tertiaryaminoalkanols can be prepared by heating the secondary amine with the appropriate haloalkanoic acid ester, followed by reduction of the thus-produced aminoalkanoic acid ester with lithium aluminum hydride according to the :method described by Mofiett, supra.
  • the conversion of the tertiaryaminoalkanols so obtained to the corresponding tertiaryaminoalkyl halides can be carried out by the use of known halogenating agents such as thionyl bromide, thionyl chloride, phosphorus tribromide, phosphorus trichloride, and the like, using, for example, the procedure described by Moffett et al., I. Am. Chem. Soc. 77, 1565, 1955.
  • ot-tetralones (II) which are employed as starting materials in the process of the invention can be prepared by the following methods. For example, they can be prepared according to the following reaction scheme:
  • alk-oxy and x have the significance hereinbefore described with the exceptions noted above.
  • the appropriately substituted alkyl phenyl ketone (V1) is condensed with benzaldehyde (VII) to produce the corresponding chalcone (VIII) under conditions conventionlly employed in the preparation of chalcones, for example, by condensation of (VI) and (VII) in the presence of a base such as sodium hydroxide, potassium hydroxide, and the like, in an inert solvent such as a mixture of water and a lower alkanol, for example, methanol, ethanol, and the like.
  • a base such as sodium hydroxide, potassium hydroxide, and the like
  • an inert solvent such as a mixture of water and a lower alkanol, for example, methanol, ethanol, and the like.
  • the reaction is generally conducted at or below room temperature with external cooling as required.
  • the chalcone (VIII) is isolated from the reaction mixture and purified by conventional procedures, for example, by solvent extraction followed by distillation, in the case of a liquid product, or
  • the chalcone (VIII) so obtained is then converted to the corresponding nitrile (IX) by reaction with hydrogen cyanide, for example, by treatment with an alkali metal cyanide such as potassium cyanide, sodium cyanide, and the like in the presence of acetic acid and an inert solvent such as aqueous methanol, aqueous ethanol and the like, using the procedure described by Newman, J. Am. Chem. Soc. 60, 2947, 1938 for the conversion of benzalacetophenone (chalcone) to a-phenyl-B-benzoylpropionitrile.
  • the desired nitrile (IX) generally separates from the reaction mixture as a solid and can be isolated by filtration and purified by recrystallization.
  • the nitrile (IX) so obtained is hydrolyzed to the corresponding keto acid (X) by conventional procedures for the hydrolysis of nitriles, for example, by heating under reflux in the presence of aqueous mineral acid such as sulfuric acid until hydrolysis is substantially complete.
  • the desired acid (X) generally separates from the reaction mixture as a solid and is isolated by filtration and purified by recrystallization or by other conventional procedures, for example, by conversion to an alkali metal salt followed by acidification of the latter to regenerate the free acid.
  • the keto acid (X) so obtained is then subjected to reduction to form the corresponding acid (XI).
  • the reduction can be effected using any of the methods customarily employed for the conversion of a keto group to a methylene group.
  • a particularly suitable reducing agent is amalgamated zinc and treatment of the keto acid (X) with amalgamated zinc in the presence of a mineral acid affords the desired acid (X1) in excellent yield.
  • the acid (XI) can be isolated from the reaction mixture by conventional procedures, for example, by decantation of the liquid reaction mixture, followed by solvent extraction of the decanted liquid and evaporation of the solvent. Generally speaking, the acid (XI) so obtained is sufficiently pure to be used in the next step of the synthesis without further treatment.
  • the acid (XI) so obtained can be purified by conventional procedures, for example, by distillation in the case of a liquid or recrystallization in the case of a solid or by conversion to an alkali metal salt followed by acidification of the latter to yield the free acid.
  • Lewis acid is well known in the art and is defined succinctly by Fieser and Fieser, Organic Chemistry, third edition, page 13 8 (Reinhold, 1956).
  • Lewis acid is well known in the art and is defined succinctly by Fieser and Fieser, Organic Chemistry, third edition, page 13 8 (Reinhold, 1956).
  • Examples of such compounds are hydrogen fluoride, boron trifluoride, arsenic trifluoride, phosphorus pentafluoride, titanium tetrafluoride, concentrated sulfuric acid, polyphosphoric acid, and the like.
  • the preferred Levvis acid for use in the above process is hydrogen fluoride.
  • a particularly convenient method of cyclizing the acid (XI) according to the above procedure comprises adding the acid (XI) to liquid hydrogen fluoride with stirring and then allowing the hydrogen fluoride to evaporate at about Z030 C.
  • the desired a-tetralone (II) is then isolated from the residue by conventional methods, for example, by dissolving the residue in a suitable solvent such as ether, washing the solution so obtained with an aqueous solution of a base such as sodium carbonate, sodium hydroxide, and the like, and then evaporating the washed solution to dryness.
  • the a-tetralone (II) so obtained can be purified, if desired, by conventional procedures, for example, by recrystallization.
  • the acid (XI) can be cyclised to the a-tetralone (II) by conversion of the acid (X I) to the corresponding acid chloride and treatment of the latter with aluminum chloride or stannic chloride according to the procedure described by [F-ieser et al., I. Am. Chem. Soc. 60, 170, 1938.
  • alkyl phenyl ketones (VI) which are employed as starting materials in the above-described synthesis of the u-tetralones (II) can be prepared from the corresponding nuclear-substituted benzoic acids by conversion of the latter to the acid chlorides followed by reaction of the latter with the appropriate dialkyl cadmium according to the procedure described in Chemical Reviews 40, 15, 1947. Many of the alkyl phenyl ketones (VI) are known in the literature.
  • the acid addition salts of the compounds of the inventionhaving the Formula I can be prepared by methods well known in the art.
  • the acid addition salts of the invention can be prepared by reacting a free base having the Formula I with a pharmacologically acceptable acid, as hereinbefore defined, in the presence of an inert solvent such as methanol, ethanol, and the like.
  • the N-oxide compounds of the invention can be prepared by methods well known in the art, for example, by reacting the free base of the Formula I with an oxidizing agent such as hydrogen peroxide, peracetic acid, Caros acid, and the like. Advanta-geously, the reaction is carried out at ordinary temperatures (e.g., of the order of 20 to 30 C.) in the presence of an inert solvent such as benzene, chloroform, lower-alkyl alkanoates such as ethyl acetate, and lower alkanols such as methanol, ethanol, isopropyl alcohol, and the like.
  • an inert solvent such as benzene, chloroform, lower-alkyl alkanoates such as ethyl acetate, and lower alkanols such as methanol, ethanol, isopropyl alcohol, and the like.
  • the oxidizing agent is employed in at least stoichiometric proportion with respect to the free base (I) and preferably the oxidizing agent is present in a slight excess.
  • any excess of oxidizing agent can be removed by treating the reaction mixture with an agent such as platinum oxide, palladium, Raney nickel, and inorganic hydrosulfites, such as sodium hydrosulfite, and the like.
  • the N-oxide acid addition salts of the invention can be prepared from the corresponding N-oxide and a pharmacologically acceptable acid using the procedures hereinbefore described for the preparation of the acid addition salts of the compounds (I)
  • the quaternary ammonium salts of the invention can be prepared by reacting a [free base of the Formula I with a quaternating agent, for example, an alkyl halide such as methyl iodide, ethyl chloride, isopropyl bromide, and the like, an alkenyl halide such as allyl chloride, allyl bromide, and the like, a dialkyl sulfate such as dimethyl sulfate, diethyl sulfate, and the like, an aralkyl halide such as benzhydryl chloride, phenethyl bromide, and the like, or an alkyl arylsulfonate such as methyl p-toluene
  • the reaction is effected by heating the reactants together in the presence of an inert solvent such as acetonitrile, acetone, methanol, ethanol, and the like.
  • an inert solvent such as acetonitrile, acetone, methanol, ethanol, and the like.
  • the desired quaternary salt separates from solution upon cooling the reaction mixture and can be isolated by filtration. Purification of the quaternary salt can be effected by conventional methods, rfor example, by recrystallization.
  • a mixture of 1 g. of 2 phenyl-4-( 3methoxyphenyl)-4- hydroxyvaleric acid, 100 mg. of p-toluenesulfonic acid and 1 00 ml. of benzene is heated under reflux with removal of evolved water until no further water is eliminated from the reaction mixture.
  • the residual solution is extracted with an excess of aqueous sodium hydroxide solution and the latter is acidified with hydrochloric acid.
  • the solid which separates is isolated by filtration, washed with water, and dried.
  • Examples 1 through 19 below illustrate the preparation of representative 2-phenyl1 [(p-tentiaryaminoalkoxy) phenyl]-3,4-dihydronaphthalene free bases and acid addition salts, quaternary ammonium salts, N-ioxides, and N-oxide acid addition salts thereof.
  • the corresponding Z-phenyl-l-[oand m- (tertiaryaminoalkoxy) phenyl] -3,4- dihydronaphthalene free bases and acid addition salts, quaternary ammonium salts, N-oxides, and N-oxide acid addition salts thereof are prepared as follows.
  • EXAMPLE 1 1 [p (Z-diethylaminoethoxy phenyl] -2-phenyl-6-meth oxy- 3,4-dihydr0naphthalene and the hydrochloride zhereo] To 0.73 g. of dry magnesium chips maintained in an atmosphere of nitrogen was added 5 ml. of tetrahydrofuran and 4 drops of methyl iodide and the mixture was stirred until reaction stanted. To the resulting mixture was added a solution of 8.15 g. of p-(2-diethylaminoethoxyybromobenzene in ml. of tetrahyd-rofuran.
  • a solution of 1 g. of the above hydrochloride in water was made basic by the addition of aqueous sodium hydroxide solution.
  • the basic solution was extracted with ether, washed with water and dried over anhydrous sodium sulfate.
  • the dried solution was filtered and the filtrate was evaporated to dryness.
  • the residue was recrystallized from aqueous ethanol to obtain 1-[p-(2-diethyla minoethoxy)phenyl] 2 pheny1-6-methoxy-3,4-dihydronaphthalene in the for-m of a crystalline solid.
  • EXAMPLE 2 1 [l (2 dimethylaminoethoxy)phenyl] 2 phenyl 6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p- (2- dimethylamin oethoxy)bromobenzene, there is obtained 1 [p (2 dimethylaminoethoxy)phenyl] 2 phenyl 6- methoxy-S,4-dihydronaphthalene and the hydrochloride thereof.
  • EXAMPLE 3 1 [p (2 diethylaminopropoxy)phenyl] 2 phenyl 6- methoxy-3,4-dihydronaphtha'lene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-diethylaminoethoxy)bromoibenzene by p-(2- diethylaminopropoxy)bromobenzene, there is obtained 1 -[p (2 diethylaminopr-opoxy)phenyl] 2 phenyl 6- methoxy-S,4-dihydronaphthalene and the hydrochloride thereof.
  • EXAMPLE 6 1 [p (3 diethylaminobwtoxy)phenyl] 2 phenyl 6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2+diethylam-inoethoxy)bromobenzene by p-(3- diethylaminobutoxy)bromobenzene, there is obtained 1 [p (3 -diethylaminobutoxy)phenyl] 2 phenyl 6- methoXy-3,4-dihydron-aphthalene and the hydrochloride thereof.
  • EXAMPLE 8 l [p (2 diethylaminopentoxy)phenyl] 2 phenyl 6- meth0xy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p-(6- dime thylaminohexyloxy) bromobenzene, there is obtained 1-[p-(6-dimethylaminohexyloxy)phenyl] 2 phenyl 6- methoXy-3,4-dihydronaphthalene and the hydrochloride thereof.
  • EXAMPLE 10 1 [p (2 pyrrolidinoethoxy)phenyl] 2 phenyl 6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p- (2- pyrrolidinoethoxy)bromobenzene, there is obtained l-[p- (2 pyrrolidinoethoxy)phenyl] 2 phenyl 6 methoXy- 3,4-dihydronaphthalene and .the hydrochloride thereof, which latter has a melting point of 168 to 172 C.
  • EXAMPLE 11 1- ⁇ p [3 (2,2 dimethylpyrrolidino)propoxy]phenyl ⁇ -2- phenyl-6-methoxy-3,4-dihydr0naphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-d-iethylaminoethoxy)bromobenzene by p-[3- (2,2-dimethy1pyrrolidino)propoxy]bromobenzene, there is obtained l- ⁇ p [3 (2,2 dimethylpyrrolidino)propoxy]- phenyl ⁇ -2 phenyl-6-methoXy-3,4-dihydronaphthalene and the hydrochloride thereof.
  • EXAMPLE 12 J-[p-(Z-piperidinoethoxy)phenyl] 2 phenyl-6-methoxy- 3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-diethylaminoethoxy)bromobenzene by p-(2- piperidinoethoxy)bromobenzene, there is obtained 1-[p (2 -piperidinoethoxy)phenyl] 2 phenyl 6 methoxy- 3,4-dihydronaphthalene and the hydrochloride thereof, which latter has a melting point of 216 to 219 C.
  • EXAMPLE 13 1 -[p- (2 morpholinoetho-xy) phenyl] -2-phenyl-6-methoxy- 3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p-(2- morpholinoethoxy)bromobenzene, there is obtained 'l-[p- (Z-morpholinoeth oxy)phenyl] 2 phenyl 6 methoxy- 3,4-dihydronaphthalene and the hydrochloride thereof, which latter has a melting point of 200 to 204 C.
  • EXAMPLE 14 J- ⁇ p-[Z-(l' methyl 4' piperazino)ethoocy]phenyl ⁇ 2- phenyl 6 methoxy 3,4 dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p-[2- (l-methyl-4'-piperazino)ethoxy]bromobenzene, there is obtained 1 ⁇ p [2-(1 methyl 4 piperazino)et1hoxy]- p heny1 ⁇ -2-phenyl-6-methoXy-3,4-dihydronaphthalene and the hydrochloride thereof.
  • EXAMPLE 15 l-[p (2-hexamethyleneim-in0elhoxy)phenyl] -2-phenyl-6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p 2-diethylaminoethoxy) bromobenzene by p-(2- hexamethyleneiminoethoxy)bromobenzene, there is obtained 1 [p (2 hexamethyleneiminoethoxy)phenyl]-2- phenyl-6-methoxy-3,4-dihydronaphthalene and the hydrochloride thereof.
  • EXAMPLE 16 1 [p- (Z-homopiperazinoethoxy phenyl] -2-phenyl-6-methoxy 3,4 dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-diethylaminoethoxy)bromobenzene by p-(2- homopiperazinoethoxy)bromobenzene, there is obtained 1 -[p-(Z homopiperazinoethoxy) phenyl]-2-phenyl-6-methoxy-3,4-dihydronaphthalene and the hydrochloride there of.
  • EXAMPLE 17 1 [p (2-homom0rpholinoethoxy)phenyl] 2 phenyl-6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-diethylaminoethoxy)-bromobenzene by p-(2- homomorpholinoethoxy)bromobenzene, there is obtained 1 [p (2 homomorpholinoethoxy)phenyl] 2-phenyl-6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof.
  • EXAMPLE 18 1 [p- (Z-diethylaminoethoxy )phenyl] -2-phenyl-6-methoxy- 3,4-dihydronaphthalene methiodide A solution of 1 g. of 1-[p-(Z-diethylaminoethoxy)phenyl]-2-phenyl-6-methoxy-3,4-dihydronaphthalene in 12 ml. of acetonitrile is cooled in ice. To the cooled solution is added 1.5 ml. of methyl iodide and the mixture is allowed to stand overnight before being poured into 100 ml. of ether.
  • EXAMPLE 19 1 [p-(2 diethylaminoethoxy)phenyl]-2-phenyl-6-methoxy-3,4-dihydronaphthalene N-oxide and the hydrochloride thereof To a solution of 1-[p-(Z-diethyIaminoeth-oxy)phenyl]-2- phenyl-6-methoxy-3,4-dihydronaphthalene in 50 ml. of absolute ethanol is added an equimolar quantity of 30% hydrogen peroxide. The mixture is allowed to stand for 4 days at room temperature, at the end of which time the mixture is shaken with 0.5 g. of platinum oxide until a test for peroxide is negative.
  • N-oxide so obtained is converted to the corresponding hydrochloride by dissolving the N-oxide in ether and treating the ether solution with an excess of a saturated solution of hydrogen chloride in ether.
  • the solid which separates is isolated by filtration. There is thus obtained 1- [p- Z-diethylaminoethoxy) phenyl] -2-phenyl-6- methoxy-3,4-dihydronaphthalene N-oxide hydrochloride.
  • EXAMPLE 20 ride 1250 Dicalcium phosphate 2500 Methylcellul-ose, U.S.P. (15 cps.) 65 Talc, bolted 450 Calcium stearate, fine powder 35
  • the powdered 1-[p-Z-diethylaminoethoxy)phenyl]-2- phenyl-6-methoxy-3,4-dihydronaphth-alene hydrochloride and the calcium phosphate are mixed Well and granulated with a 7.5% aqueous solution of the methylcellulose.
  • the granules are passed through a No. 8 screen and dried carefully at F.
  • the dried granules are passed through a No. 12 screen, mixed thoroughly with the talc and calcium stearate, and compressed into tablets.
  • R and R are selected from the class consisting of lower-alkyl from 1 to 8 carbon atoms, inclusive, and together with the nitrogen atom, a member selected from :the class consisting of pyrrolidino, Z-methylpyrrolidino, 2,2-dimethylpyrrolidino, piperazino, 4-methy1piperazino, 2,4-dimethylpiperazino, morpholino, piperidino, Z-methylpiperidino, 3-methylpiperidino, hexamethyleneimino, homopiperazino and homomorpholino,
  • C H represents alkylene from 2 to 6 carbon atoms, inclusive, alkoxy has from 1 to 8 carbon atoms, inclusive, and x is an integer from 1 to 4, inclusive;
  • quaternary ammonium salts of compounds of the above formula selected from the class consisting of lower-alkyl quaternary ammonium halides, loweralkenyl quaternary ammonium halides, lower-alkyl quaternary ammonium sulfates, aralkyl quaternary ammonium halides, and lower-alkyl quaternary arylsulfonates.
  • alkoxy 4 wherein R and R are selected from the class consisting of lower-alkyl from 1 to 8 carbon atoms, inclusive, and together with the nitrogen atom, a member selected from the class consisting of pyrrolidino, Z-methylpyrrolidino, 2,2-dimethylpyrrolidino, piperazino, 4-methylpiperazino, 2,4-dimethylpiperazino, m'orpholino, piperidino, Z-methylpiperidino, 3-methylpiperidino, hexamethyleneimino, homopiperazino and homomorpholino, C H represents alkylene from 2 to 6 carbon atoms, inclusive, and alkoxy has from 1 to 8 carbon atoms, inclusive;
  • quaternary ammonium salts of compounds of the above formula selected from the class consisting of lower-alkyl quaternary ammonium halides, loweralkenyl quaternary ammonium halides, loWer-alkyl quaternary ammonium sulfates, aralkyl quaternary ammonium halides, and lower-alkyl quaternary arylsulfonates.

Description

United States Patent 3,274 213 ALKOXY-SUBSTITUTED 2-PHENYL-1-(TERTIARY- AMINOALKOXY)PHENYL-3,4-DIHYDRONAPH- THALENES Daniel Lednicer, Portage Township, Kalamazoo County, Mich., assignor to The Upjohn Company, Kalamazoo, Mich., a corporation of Delaware No Drawing. Original application Sept. 5, 1961, Ser. No. 135,767. Divided and this application July 23, 1963,
Ser. No. 296,939
8 Claims. (Cl. 260326.5)
This invention relates to novel 3,4-dihydronaphthalenes and is more particularly concerned with novel alkoxy substituted 2-phenyl-l-(tertiaryaminoalkoxy) phenyl-3,4-dihydronaphthalenes and acid addition salts, quaternary ammonium salts, N-oxides and N-oxide acid addition salts thereof, and with processes for their preparation.
This copending application is a division of application Serial No. 135,767, filed September 5, 1961.
The novel compounds of the invention are selected from the class consisting of (a) the free bases, (b) the pharmacologically acceptable acid addition salts, (c) the N-oxides, (d) the N-oxide pharmacologically acceptable acid addition salts, and (e) the quaternary ammonium salts of compounds having the formula:
wherein R and R are selected from the class consisting of lower-alkyl and lower-alkyl linked together to form a 5 to 7 ring atom saturated heterocyclic radical, one of the ring atoms of which, in addition to the amino nitrogen atom, is selected from the class consisting of carbon nitrogen, and oxygen, the other ring atoms being carbon, C H represents alkylene from 2 to 6 carbon atoms, inclusive, alkoxy contains from 1 to 8 carbon atoms, inclusive, and x is an integer from 1 to 4, inclusive.
The term lower-alkyl means an alkyl group containing from 1 to 8 carbon atoms, inclusive, such as methyl, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, and isomeric forms thereof. Examples of alkoxy containing from 1 to 8 carbon atoms, inclusive, are methoxy, ethoxy, propoxy, butoxy, amyloxy, hexyloxy, heptyloxy, octyloxy, and isomeric forms thereof.
The term lower alkyl groups linked together to form a 5 to 7 ring atom saturated heterocyclic radical, one of the ring atoms of which, in addition to the amino nitrogen atom, is selected from the class consisting of carbon, nitrogen, and oxygen, the other ring atoms being carbon is inclusive pyrrolidino, Z-methylpyrrolidino, 2,2- dimethylpyrrolidino, and like alkylpyrrolidino groups, piperazino, 4-methylpiperazino, 2,4-dimethylpiperazino, and like alkylpiperazino groups, morpholino, piperidino, Z-methylpiperidino, 3-methylpiperidino, and like alkylpiperidino groups, hexamethyleneimino, homopiperazino, homomorpholino, and the like.
The acid addition salts of the invention comprise the salts of the compounds having the Formula I and of the "ice corresponding N-oxides with pharmacologically acceptable acids such as sulfuric, hydrochloric, nitric, phosphoric, lactic, benzoic, methane-sulfonic, p-toluenesulfonic, salicylic, acetic, propionic, maleic, malic, tartaric, citric, cyclohexylsulfamic, succinic, nicotinic, ascorbic acids, and the like.
The quaternary ammonium salts of the invention are the salts obtained by reacting the free bases having the Formula I with quaternating agents, for example, lower alkyl halides, lower-alkenyl halides, di(lower-alkyl) sulfates, aralkyl halides, lower-alkyl arylsulfonates, and the like. The term lower-alkyl has the meaning hereinbefore defined. The term aralkyl means an aralkyl group containing from 7 to 13 carbon atoms, inclusive, such as benzyl, phenethyl, phenylpropyl, benzhydryl, and the like. Examples of quaternary salts of the compounds of Formula I are the methobromide, methiodide, ethobromide, propyl chloride, butyl bromide, octyl bromide, methyl methosulfate, ethyl ethosulfate, allyl chloride, allyl bromide, benzyl bromide, benzhydryl chloride, methyl toluenesulfonate, and the like.
The novel compounds of the invention, including the free bases of Formula I, the acid addition salts thereof, the quaternary ammonium salts thereof, and the corresponding N-oxides and N-oxide acid addition salts possess pharmacological activity. Illustratively, the compounds of the invention are useful as anti-inflammatory agents, antifertility agents, antiestrogenic agents, and as agents for the lowering of cholesterol blood levels in mammals including man and animals of economic value. For purposes of administration to mammals, the novel compounds of the invention can be employed per se, for example, enclosed in a hard capsule for oral administration, or can be combined with solid or liquid pharmaceutical carriers and formulated in the form of tablets, powder packets, or capsules, using starch and like excipients, or dissolved or suspended in suitable solvents or vehicles, for oral or parenteral administration.
In addition to their pharmacological activity, the compounds of the invention are also useful as intermediates. For example, the compounds having the Formula I can be reacted with fiuosilicic acid to form the fluosilicate salts which in dilute aqueous solution are effective mothproofing agents as more fully disclosed in US. Patents 2,075,359 and 1,915,334.
The novel compounds of the invention having the Formula I can be prepared by reaction of an appropriately substituted l-keto-1,2,3,4-tetrahydronaphthalene (i.e., an a-tetralone) having the formula:
[alkoxy]; v
wherein alkoxy and x have the significance hereinbefore defined (with the exception noted below), with a Grignard reagent have the formula:
(III) an inert solvent under anhydrous conditions in accordance with the established procedure for Grignard reactions. Suitable inert solvents include diisopropyl ether, diisobutyl ether, tetrahydrofuran, and the like. The reaction can be carried out at temperatures within the range of about C. to about the boiling point of the solvent employed and is preferably carried out at elevated temperatures, for example, at or near the boiling point of the reaction mixture.
The reaction time varies within wide limits according to the temperature at which the reaction is conducted. Generally speaking, where the reaction is carried out at elevated temperatures such as the boiling point of the reaction mixture, it is necessary to employ a reaction time of the order of several hours to ensure completion of the reaction.
The desired dihydron-aphthaleue having the Formula I can be isolated from the reaction mixture by conventional procedures, for example, by decomposing the reaction mixture with water, ammonium chloride, and the like, followed by separation of the organic layer and removal of solvent therefrom. In many cases, the product so obtained is largely the desired compound (I) contaminated with minor impurities and unchanged starting material which can be removed by simple procedures, for example by isolation of the desired compound (I) as an acid addition salt.
However, in some cases the desired 3,4-di-hydronaphth-alene (I) is contaminated with appreciable quantities of the corresponding 1 hydroxy 1,2,3,4 tetrahydronaphthalene having the formula (IV) below and in certain cases the reaction product obtained is largely this compound containing only a small amount of the desired compound In the above formula R R C H alkoxy and x have the significance hereinbefore defined.
The compound (IV), when obtained as the major reaction product or when present in significant quantities in the above-described reaction product, can be converted to the desired compound (I) by dehydration. The dehydration can be effected in most instances by heating the compound (IV) in a solvent such as benzene, toluene, xylene, and the like which forms an azeotrope with water, in the presence of a trace of a strong acid such as hydrochloric, sulfuric, p-toluenesulforn'c acids and the like. The water which is formed in the dehydration is removed from the reaction mixture azeotropically. There is thereby obtained a solution of the desired compound (I) from which the latter can be isolated by evaporation or other conventional procedures.
In certain cases, the dehydration of the l-hydroxy-l,2, 3,4-tetrahydronaphthalene (IV) requires more drastic conditions such as heating the compound at, or slightly above, its melting point, preferably in the presence of an inert gas, until evolution of water is complete.
The Grignard reagents having the Formula III which are employed as starting materials in the process of the invention can be prepared by reaction of magnesium in an anhydrous inert organic solvent such as diisopropyl ether,
dibutyl ether, tetrahydrofuran, and the like with the appropriately substituted halobenzene having the formula:
wherein R R C H and Hal have the significance hereinbefore defined, using procedures well-known in the art for the preparation of Grignard reagents.
' The halobenzenes having the Formula V can be prepared by etherification of the corresponding halophenol with the appropriate tertiaryaminoalkyl halide N CnH2n-Ha1 R2 wherein R R and C H and Hal have the significance hereinbefore defined. The etherification is conducted advantage'ously in an inert solvent such as a lower alkanol,
for example, methanol, ethanol, isopropyl alcohol, and
the like in the presence of a base such as sodium hydroxide, sodium methoxide, and the like.
The tertiaryaminoalkyl halides having the formula NH R2 wherein R and R have the significance herein'before defined, with the appropriate haloalkanol, HalC H ,,OH, wherein Hal and C H have the significance hereinbefore defined, in accordance with known methods. The condensation between the secondary amine NH R2 and the haloalkanol Hal-C H OH can be carried out. for example, using the procedure described by Moffett. J. Org. Chem. 14, 862, 1949. Alternatively, the desired tertiaryaminoalkanols can be prepared by heating the secondary amine with the appropriate haloalkanoic acid ester, followed by reduction of the thus-produced aminoalkanoic acid ester with lithium aluminum hydride according to the :method described by Mofiett, supra. The conversion of the tertiaryaminoalkanols so obtained to the corresponding tertiaryaminoalkyl halides can be carried out by the use of known halogenating agents such as thionyl bromide, thionyl chloride, phosphorus tribromide, phosphorus trichloride, and the like, using, for example, the procedure described by Moffett et al., I. Am. Chem. Soc. 77, 1565, 1955.
The ot-tetralones (II) which are employed as starting materials in the process of the invention can be prepared by the following methods. For example, they can be prepared according to the following reaction scheme:
alko x I wig CH3 HA3 3/ H H 0 O (VII) In the above reaction sequence, alk-oxy and x have the significance hereinbefore described with the exceptions noted above.
In the above reaction sequence, the appropriately substituted alkyl phenyl ketone (V1) is condensed with benzaldehyde (VII) to produce the corresponding chalcone (VIII) under conditions conventionlly employed in the preparation of chalcones, for example, by condensation of (VI) and (VII) in the presence of a base such as sodium hydroxide, potassium hydroxide, and the like, in an inert solvent such as a mixture of water and a lower alkanol, for example, methanol, ethanol, and the like. The reaction is generally conducted at or below room temperature with external cooling as required. The chalcone (VIII) is isolated from the reaction mixture and purified by conventional procedures, for example, by solvent extraction followed by distillation, in the case of a liquid product, or recrystallization in the case of a solid prodmet.
The chalcone (VIII) so obtained is then converted to the corresponding nitrile (IX) by reaction with hydrogen cyanide, for example, by treatment with an alkali metal cyanide such as potassium cyanide, sodium cyanide, and the like in the presence of acetic acid and an inert solvent such as aqueous methanol, aqueous ethanol and the like, using the procedure described by Newman, J. Am. Chem. Soc. 60, 2947, 1938 for the conversion of benzalacetophenone (chalcone) to a-phenyl-B-benzoylpropionitrile. The desired nitrile (IX) generally separates from the reaction mixture as a solid and can be isolated by filtration and purified by recrystallization.
The nitrile (IX) so obtained is hydrolyzed to the corresponding keto acid (X) by conventional procedures for the hydrolysis of nitriles, for example, by heating under reflux in the presence of aqueous mineral acid such as sulfuric acid until hydrolysis is substantially complete. The desired acid (X) generally separates from the reaction mixture as a solid and is isolated by filtration and purified by recrystallization or by other conventional procedures, for example, by conversion to an alkali metal salt followed by acidification of the latter to regenerate the free acid.
The keto acid (X) so obtained is then subjected to reduction to form the corresponding acid (XI). The reduction can be effected using any of the methods customarily employed for the conversion of a keto group to a methylene group. A particularly suitable reducing agent is amalgamated zinc and treatment of the keto acid (X) with amalgamated zinc in the presence of a mineral acid affords the desired acid (X1) in excellent yield. The acid (XI) can be isolated from the reaction mixture by conventional procedures, for example, by decantation of the liquid reaction mixture, followed by solvent extraction of the decanted liquid and evaporation of the solvent. Generally speaking, the acid (XI) so obtained is sufficiently pure to be used in the next step of the synthesis without further treatment. [if desired, however, the acid (XI) so obtained can be purified by conventional procedures, for example, by distillation in the case of a liquid or recrystallization in the case of a solid or by conversion to an alkali metal salt followed by acidification of the latter to yield the free acid.
In the final stage of the synthesis the acid (XI) is cyclized to the required a-tetralone (I I) in the presence of a Lewis acid, using the general procedure described by Fieser and Hershberg, I. Am. Chem. Soc. 61, 1272, 1939. The term Lewis acid is well known in the art and is defined succinctly by Fieser and Fieser, Organic Chemistry, third edition, page 13 8 (Reinhold, 1956). Examples of such compounds are hydrogen fluoride, boron trifluoride, arsenic trifluoride, phosphorus pentafluoride, titanium tetrafluoride, concentrated sulfuric acid, polyphosphoric acid, and the like. The preferred Levvis acid for use in the above process is hydrogen fluoride.
A particularly convenient method of cyclizing the acid (XI) according to the above procedure comprises adding the acid (XI) to liquid hydrogen fluoride with stirring and then allowing the hydrogen fluoride to evaporate at about Z030 C. The desired a-tetralone (II) is then isolated from the residue by conventional methods, for example, by dissolving the residue in a suitable solvent such as ether, washing the solution so obtained with an aqueous solution of a base such as sodium carbonate, sodium hydroxide, and the like, and then evaporating the washed solution to dryness. The a-tetralone (II) so obtained can be purified, if desired, by conventional procedures, for example, by recrystallization.
Alternatively, the acid (XI) can be cyclised to the a-tetralone (II) by conversion of the acid (X I) to the corresponding acid chloride and treatment of the latter with aluminum chloride or stannic chloride according to the procedure described by [F-ieser et al., I. Am. Chem. Soc. 60, 170, 1938.
The alkyl phenyl ketones (VI) which are employed as starting materials in the above-described synthesis of the u-tetralones (II) can be prepared from the corresponding nuclear-substituted benzoic acids by conversion of the latter to the acid chlorides followed by reaction of the latter with the appropriate dialkyl cadmium according to the procedure described in Chemical Reviews 40, 15, 1947. Many of the alkyl phenyl ketones (VI) are known in the literature.
An alternative method -for the preparation of the octetralones of Formula II is that described 'by Newman, I. Am. Chem. Soc. 62, 2295, 1940, for the preparation of 2-o-tolyl-3-methyl-aatetralone. The method comprises reacting the benzyl cyanide with the appropriately substituted phenethyl bromide [alkoxy] X CHzCHzBr (al-koxy and x having the significance hereinbefore defined) in the presence of sodamide and 'hydrolyzin-g the resulting nitrile to give the corresponding acid (XI) which is then cyclized as hereinbefore described to the a-tetralone (I I).
The acid addition salts of the compounds of the inventionhaving the Formula I can be prepared by methods well known in the art. For example, the acid addition salts of the invention can be prepared by reacting a free base having the Formula I with a pharmacologically acceptable acid, as hereinbefore defined, in the presence of an inert solvent such as methanol, ethanol, and the like.
The N-oxide compounds of the invention can be prepared by methods well known in the art, for example, by reacting the free base of the Formula I with an oxidizing agent such as hydrogen peroxide, peracetic acid, Caros acid, and the like. Advanta-geously, the reaction is carried out at ordinary temperatures (e.g., of the order of 20 to 30 C.) in the presence of an inert solvent such as benzene, chloroform, lower-alkyl alkanoates such as ethyl acetate, and lower alkanols such as methanol, ethanol, isopropyl alcohol, and the like. Suitably the oxidizing agent is employed in at least stoichiometric proportion with respect to the free base (I) and preferably the oxidizing agent is present in a slight excess. When the reaction has been completed, any excess of oxidizing agent can be removed by treating the reaction mixture with an agent such as platinum oxide, palladium, Raney nickel, and inorganic hydrosulfites, such as sodium hydrosulfite, and the like.
The N-oxide acid addition salts of the invention can be prepared from the corresponding N-oxide and a pharmacologically acceptable acid using the procedures hereinbefore described for the preparation of the acid addition salts of the compounds (I) The quaternary ammonium salts of the invention can be prepared by reacting a [free base of the Formula I with a quaternating agent, for example, an alkyl halide such as methyl iodide, ethyl chloride, isopropyl bromide, and the like, an alkenyl halide such as allyl chloride, allyl bromide, and the like, a dialkyl sulfate such as dimethyl sulfate, diethyl sulfate, and the like, an aralkyl halide such as benzhydryl chloride, phenethyl bromide, and the like, or an alkyl arylsulfonate such as methyl p-toluenesulfonate, and the like. Preferably the reaction is effected by heating the reactants together in the presence of an inert solvent such as acetonitrile, acetone, methanol, ethanol, and the like. Generally speaking, the desired quaternary salt separates from solution upon cooling the reaction mixture and can be isolated by filtration. Purification of the quaternary salt can be effected by conventional methods, rfor example, by recrystallization.
The following preparations and examples are illustrative of the process and products of the present invention, but are not to be construed as limiting.
PREPARATION 1 p- (Z-diethylaminoethoxy) bromobenzene A mixture of 272 g. (1.57 moles) of p-bromophenol, 1500 ml. of ethanol, and 340 g. (equivalent to 1.57 moles of sodium methoxide) of a 25% solution of sodium methoxide in methanol was stirred and heated under reflux and to the refluxing solution was added dropwise, over a period of 30 minutes, a solution of 213 g. of 2- diethylaminoethyl chloride in 200 ml. of ethanol. After the addition was complete the mixture was stirred and heated under reflux for a further 3 hours. At the end of this time the reaction "mixture was cooled and filtered, and the filtrate was evaporated under reduced pressure. The residual oil was dissolved in 1500 ml. of ether and the ether solution was washed with two ZOO-ml. portions of dilute aqueous sodium hydroxide solution and then with four 200-ml. portions of water. The ethereal solution was dried over anhydrous magnesium sulfate, and the filtrate was evaporated. The residue was distilled under reduced pressure and that fraction having a boiling point of 110-115 C. at 'a pressure of 0.3 mm. of mercury was collected. There was thus obtained 310 g.
of p-(2-diethylaminoethoxy)bromobenzene in the form of an oil. The free base so obtained was converted to the hydrochloride having a melting point of 139 to 140 C.
'8 Analysis.Calcd. for C H BrClNO: C, 46.69; H,
6.20; N, 4.54. Found: C, 47.04; H, 6.47; N, 4.49.
Using the above procedure, but replacing the Z-diethylaminoethyl chloride by 3-dimethylaminopropyl chloride, 2 diethylarninopropyl chloride, 2 dibutylaminoethyl bromide, 2 methylethylaminoethyl bromide, 3 diethylaminobutyl chloride, 5-dimethylaminopen tyl bromide, 2 diethylaminopentyl bromide, 6 dimethylaminohexyl chloride, 2 pyrrolidinoethyl chloride, 3- (2,2 dimethylpyrrolidino)propyl bromide, 2 piperidinoethyl chloride, 2 piperidinopropyl bromide, 2- morpholinoethyl chloride, 2 morpholinobutyl bromide, 1 methyl 4 (2 chloroethyl)piperazine, 2- hexamethyleneiminoethyl chloride, 2 homopiperazinoethyl chloride, and 2 -homomorpholinoethyl chloride, there are obtained p (3 dimethylaminopropoxy)bromobenzen-e, p (2 diethylaminopropoxy)bromobenzene, p (2 dibutylaminoethoxy)bromobenzene, p (2- N methyl N ethylaminoethoxy)bromobenzene, p (3- diethylaminobutoxy)bromobenzene, p (5 dimethylaminopentoxy)bromobenzene, p (2 diethylaminopentoxy)bromobenzene, p (6 dimethylaminohexyloxy)bromobenzene, p (2 pyrrolidinoethoxy)bromobenzene, p [3 (2,2 dimethylpyrrolidino)propoxy] bromobenzene, p (2 piperidinoethoxy)bromobenzene, p (2 piperidinopropoxy)bromobenzene, p (2 morpholinoethoxy)bromobenzene, p (2 morpholinobutoxy)bromobenzene, p [2 (1' methyl 4 piperazino)ethoxy]bromobenzene, p (2 hexamethyleneiminoethoxy)bromobenzene, p (2 homopiperazinoethoxy)bromobenzene, and p (2 homomorpholinoethoxy)bromobenzene, respectively.
Using the above procedure, but replacing p-bromophenol by o-bromophenol and m-bromophenol, the corresponding oand -m-(tertiaryaminoalkoxy)bromobenzenes are obtained.
PREPARATION 2 3'-methoxychalc0ne A solution of 45 g. of m-methoxyacetophenone in 75 ml. of ethanol was added to a cooled solution of 16 g. of sodium hydroxide in ml. of Water. The mixture was then placed in an ice bath and 31.8 g. of benzaldehyde was added at such a rate as to keep the temperature below 20 C. The mixture was stirred for an additional 30 minutes in the cold and was then stirred for 27 hours at room temperature. The resulting solution was extracted with ether and the extract was washed with saturated brine solution before being percolated through anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The residue was distilled under reduced pressure. There was thus obtained 50.9 g. of 3-methoxychalcone in the form of an oil having a boiling point of to C. at a pressure of 4 mm. of mercury.
PREPARATION 3 2-phenyl-4- (S-methoxyphefiyl) -4-ketobutyr0nitrile A solution of 27.8 g. of potasium cyanide in 50 ml. of water was added to a mixture of 50.9 g. of 3'-methoxychalcone, 13.0 g. of acetic acid, and 100 ml. of 95% ethanol over a period of 10 minutes. The temperature was maintained at 45 C. The turbid mixture was then stirred for 6 hours and allowed to stand overnight in the cold. The crystalline solid which had separated Was isolated by filtration, washed with ice-cold aqueous ethanol and with water, and recrystallized from ethanol. There was thus obtained 49.22 g. of 2-phenyl-4-(3-methoxyphenyl)-4-ketobutyronitrile in the form of a crystalline solid having a melting point of 96 to 101 C. The infrared spectrum of the compound (mineral oil mull) exhibited maxima at 2200*, 1660, and 1580 reciprocal centimeters.
9 PREPARATION 4 2-phenyl-4- (3-methoxyphenyl) -4-ketob wtyric acid A suspension of 49.22 g. of 2-phenyl-4-(3-methoxyphenyl)-4 ketobutyronitrile in a mixture of 140 ml. of concentrated sulfuric acid and 125 ml. of water was heated on a steam bath with vigorous stirring for 4 hours. The resulting mixture was cooled and diluted with icewater. The solid which separated was isolated by filtration and recrystallized from aqueous ethanol and then from benzene. There was thus obtained 29.5 .g. of 2- phenyl-4-(3-methoxyphenyl)-4-ketobutyric acid in the form of a crystalline solid having a melting point of 140 to 145 C. An analytical sample having a melting point of 143 to 145 C. was obtained by recrystallization from benzene.
Analysis.Calcd. for C H O C, 71.82; H, 5.67. Found: C, 72.10; H, 5.74.
PREPARATION 5 2-phenyl-4-(3-methoxyphenyl)bmyric acid A total of 300 g. of mossy zinc was washed briefly with 2.5 N hydrochloric acid and then wit-h water. The metal was covered with a solution of 6.7 g. of mercuric chloride in 500 ml. of water, and this mixture was allowed to stand for 30 minutes with occasional shaking. The liquid phase was decanted and the amalgamated metal was washed well with water. To the amalgamated zinc so produced was added a mixture of 29.3 g. of 2-phenyl- 4-(3-methoxyphenyl)-3-keto butyric acid and 400 ml. of hydrochloric acid. The mixture was heated cautiously to reflux temperature and then heated under reflux for a total of 20 hours, additional portions of hydrochloric acid being added after 5 hours and 10 hours of heating. The resulting mixture was cooled and the liquid was decanted from the solid. The solid residue was washed well with ether and the decanted liquid was extracted with ether. The ether extract and washings were combined and washed with water and then with saturated brine solution before being percolated through anhydrous magnesium sulfate. The percolate was evaporated to dryness. There was thus obtained 26.2 g. of 2-phenyl-4- (3-methoxyphenol)butyric acid in the form of a viscous oil which was employed without further purification in the process of Preparation 6. The infrared spectrum of the compound (mineral oil mull) exhibited a maximum at 1705 reciprocal centimeters.
PREPARATION 6 Z-ph enyl-d-meth xy-1,2,3,4-tetrahydro-I -naphthalenone A total of 150' ml. of liquid hydrogen fluoride was added to 26.2 g. of 2-phenyl-4-(3-methoxyphenyl)butyric acid with cooling and swirling. The resulting mixture was allowed to stand at room temperature for 3 days. The residue was dissolved in methylene chloride and the solution was poured into excess concentrated aqueous potassium carbonate solution. The organic layer was separated, washed with water and saturated brine solution, and then evaporated to dryness. The residue was dissolved in 2 l. of mixed hexanes (Skellysolve B) containing 7.5% by volume of acetone and the solution was passed through a column of magnesium silicate (Florisil) prewashed with the same solvent mixture. The eluate was evaporated to dryness and the residue (17.0 g.) was recrystallized twice \from cyclohexane. There was thus obtained 13.38 g. of 2-phenyl-6-methoxy-l,2,3,4-tetrahydro-l-naphthalenone in the form of a crystalline compound having a melting point of 113 to 116 C.
Analysis.Calcd. for C H O C, 80.92; H, 6.39. Found: C, 81.08; H, 6.35.
1 0 PREPARATION 7 2-phenyl-4-methyl-6-meth0xy-1,2,3,4- tetrahydro-Z-naphthalen0ne A solution :of 5 g. of 2-phenyl-4-(3-methoxyphenyl)-3 keto'butyric acid in 100 ml. of ether is coo-led to 0 C., and treated dropwise with stirring with 29 ml. of 3 M ethereal methyl magnesium bromide solution. When the addition is complete the mixture is stirred for several hours at room temperature and then heated under reflux for 1 hour. The reaction mixture is decomposed by the addition of ice water and dilute hydrochloric acid sol-ution. The etheral layer is separated, washed with aqueous ammonium chloride solution and with water, and then dried over anhydrous sodium sulfate. The dried solution is filtered, and the filtrate is evaporated to dryness and the residue is recrystallized from aqueous ethanol. There is thus obtained 2-phenyl-4-(3-methoxyphenyl) -4-hydroxy-valeric acid.
A mixture of 1 g. of 2 phenyl-4-( 3methoxyphenyl)-4- hydroxyvaleric acid, 100 mg. of p-toluenesulfonic acid and 1 00 ml. of benzene is heated under reflux with removal of evolved water until no further water is eliminated from the reaction mixture. The residual solution is extracted with an excess of aqueous sodium hydroxide solution and the latter is acidified with hydrochloric acid. The solid which separates is isolated by filtration, washed with water, and dried. The residue [2-phenyl-4-(3-methoxyphenyl)-3-pentenoic acid] is dissolved in ethanol and hydrogenated in the presence of palladium-on-charcoa.l catalyst until the uptake of hydrogen is complete. The resulting solution is filtered and the filtrate is evaporated to dryness. There is thus obtained 2-phenyl-4-(3-meth- |oxyphenyl)valeric acid. The latter acid is then cyclised using the procedure described in Preparation 6 to give 2 phenyl-4-metl1yl-6-methoxy 1,2,3,4-te'trahydro-l-naphthalenone.
Examples 1 through 19 below illustrate the preparation of representative 2-phenyl1 [(p-tentiaryaminoalkoxy) phenyl]-3,4-dihydronaphthalene free bases and acid addition salts, quaternary ammonium salts, N-ioxides, and N-oxide acid addition salts thereof. The corresponding Z-phenyl-l-[oand m- (tertiaryaminoalkoxy) phenyl] -3,4- dihydronaphthalene free bases and acid addition salts, quaternary ammonium salts, N-oxides, and N-oxide acid addition salts thereof are prepared as follows. The appropriate oand m- (tertiaryaminoalkoxy)bromobenzenes are substituted for the corresponding p-(tertiaryarninoailkoxy)br-omo'benzenes in Examples 1 through 17 to obtain the corresponding 2-phenyl-1-[oand m-(tertiaryaminoa'lkoxy)phenyl]-3,4-dihydronaphthalene free bases and addition salts thereof. The acid addition salts thus obtained are substituted for the corresponding 2-phenyl-l-[p-tertiaryaminoalkoxy)phenyl]-3,4-dihydronaphthalene acid addition salts in Examples 18 and 19 to obtain the corresponding quaternary ammonium salts, N-oxides, and N- oxide acid addition salts.
EXAMPLE 1 1 [p (Z-diethylaminoethoxy phenyl] -2-phenyl-6-meth oxy- 3,4-dihydr0naphthalene and the hydrochloride zhereo] To 0.73 g. of dry magnesium chips maintained in an atmosphere of nitrogen was added 5 ml. of tetrahydrofuran and 4 drops of methyl iodide and the mixture was stirred until reaction stanted. To the resulting mixture was added a solution of 8.15 g. of p-(2-diethylaminoethoxyybromobenzene in ml. of tetrahyd-rofuran. The resulting mixture was heated under reflux until substantially all of the magnesium had been consumed and to the residual solution was added with stirring a solution of 7.55 g. of 2-p'henyl-6-methoxy-1,2,3,4-tetrahydro 1-naphthalen-one in ml. of tetrahydrofuran. The mixture so obtained was heated under reflux for 16 hours before being cooled. The cooled solution was treated with ether and a small quantity of water. The gel which lll formed was removed by filtration and washed well with ether. The ether tfiltrate and washings were combined and washed with water before being dried over anhydrous sodium sulfate and evaporated to dryness. The residual oil was dissolved in a mixture of ether and benzene and the solution so obtained was extracted with excess 0.5 N hydrochloric acid. The acid extract was extracted with methylene chloride and the methylene chloride extract was evaporated to dryness. The residue (648 g.) was recrystallized from a mixture of chloroform and ethyl acetate. There was thus obtained 3.42 g. of 1-[p-(2- diethylaminoethoxy)phenyl]-2 phenyl 6 methoxy-3,4- dihydronaphthalene hydrochloride in the form of a crystalline solid having a melting point of 171 to 173 C. after partially melting and res-ol-idifying at 126 C. An analytica-l sample was obtained by drying for 96 hours at 110 C. in vacuo.
Analysis.Calcd. for C H CINO C, 75.06; H, 7.39; N, 3.02. Found: C, 74.74; H, 7.40; N, 3.03.
A solution of 1 g. of the above hydrochloride in water was made basic by the addition of aqueous sodium hydroxide solution. The basic solution was extracted with ether, washed with water and dried over anhydrous sodium sulfate. The dried solution was filtered and the filtrate was evaporated to dryness. The residue was recrystallized from aqueous ethanol to obtain 1-[p-(2-diethyla minoethoxy)phenyl] 2 pheny1-6-methoxy-3,4-dihydronaphthalene in the for-m of a crystalline solid.
EXAMPLE 2 1 [l (2 dimethylaminoethoxy)phenyl] 2 phenyl 6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p- (2- dimethylamin oethoxy)bromobenzene, there is obtained 1 [p (2 dimethylaminoethoxy)phenyl] 2 phenyl 6- methoxy-S,4-dihydronaphthalene and the hydrochloride thereof.
EXAMPLE 3 1 [p (2 diethylaminopropoxy)phenyl] 2 phenyl 6- methoxy-3,4-dihydronaphtha'lene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-diethylaminoethoxy)bromoibenzene by p-(2- diethylaminopropoxy)bromobenzene, there is obtained 1 -[p (2 diethylaminopr-opoxy)phenyl] 2 phenyl 6- methoxy-S,4-dihydronaphthalene and the hydrochloride thereof.
EXAMPLE 4 J [I (Z dibutylaminoethoxy)phenyl] 2 phenyl 6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p-(Z- dibutylaminoethoxy)bromobenzene, there is obtain l-[p- (Z-dibutylaminoethoxy)phenyl] 2 aphenyl 6 methoxy- 3,4-dihydron-aphthalene and the hydrochloride thereof.
EXAMPLE 5 I-[p (2 N methyl N ethylaminoethoxy)phenyl]-2- phenyl-6-methoxy-3,4-dihydronophthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p-(2- N-methyl N ethylaminoethoxy)bromobenzene, there is obtained 1- [p- (Z-N-methyl-N-et-hylaminoethoxy) phenyl] 2-phenyl-6-methoxy-3,4-dihydronaphthalene and the hydrochloride thereof.
EXAMPLE 6 1 [p (3 diethylaminobwtoxy)phenyl] 2 phenyl 6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2+diethylam-inoethoxy)bromobenzene by p-(3- diethylaminobutoxy)bromobenzene, there is obtained 1 [p (3 -diethylaminobutoxy)phenyl] 2 phenyl 6- methoXy-3,4-dihydron-aphthalene and the hydrochloride thereof.
EXAMPLE 7 l [p (5 dimethylaminopentoxy)phenyl] 2 phenyl-6- methoxy-3 4-dihydronophthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p-(S- dimethylaminopentoxy)bromobenzene, there is obtained 1 [p -(5 dimethylaminopentoxy)phenyl] 2 phenyl-6- methoxy-S,4-dihydronaphthaiene and the hydrochloride there-of.
EXAMPLE 8 l [p (2 diethylaminopentoxy)phenyl] 2 phenyl 6- meth0xy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p-(6- dime thylaminohexyloxy) bromobenzene, there is obtained 1-[p-(6-dimethylaminohexyloxy)phenyl] 2 phenyl 6- methoXy-3,4-dihydronaphthalene and the hydrochloride thereof. EXAMPLE 10 1 [p (2 pyrrolidinoethoxy)phenyl] 2 phenyl 6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p- (2- pyrrolidinoethoxy)bromobenzene, there is obtained l-[p- (2 pyrrolidinoethoxy)phenyl] 2 phenyl 6 methoXy- 3,4-dihydronaphthalene and .the hydrochloride thereof, which latter has a melting point of 168 to 172 C.
EXAMPLE 11 1-{p [3 (2,2 dimethylpyrrolidino)propoxy]phenyl}-2- phenyl-6-methoxy-3,4-dihydr0naphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-d-iethylaminoethoxy)bromobenzene by p-[3- (2,2-dimethy1pyrrolidino)propoxy]bromobenzene, there is obtained l-{p [3 (2,2 dimethylpyrrolidino)propoxy]- phenyl}-2 phenyl-6-methoXy-3,4-dihydronaphthalene and the hydrochloride thereof.
EXAMPLE 12 J-[p-(Z-piperidinoethoxy)phenyl] 2 phenyl-6-methoxy- 3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-diethylaminoethoxy)bromobenzene by p-(2- piperidinoethoxy)bromobenzene, there is obtained 1-[p (2 -piperidinoethoxy)phenyl] 2 phenyl 6 methoxy- 3,4-dihydronaphthalene and the hydrochloride thereof, which latter has a melting point of 216 to 219 C.
EXAMPLE 13 1 -[p- (2 morpholinoetho-xy) phenyl] -2-phenyl-6-methoxy- 3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p-(2- morpholinoethoxy)bromobenzene, there is obtained 'l-[p- (Z-morpholinoeth oxy)phenyl] 2 phenyl 6 methoxy- 3,4-dihydronaphthalene and the hydrochloride thereof, which latter has a melting point of 200 to 204 C.
EXAMPLE 14 J-{p-[Z-(l' methyl 4' piperazino)ethoocy]phenyl} 2- phenyl 6 methoxy 3,4 dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(Z-diethylaminoethoxy)bromobenzene by p-[2- (l-methyl-4'-piperazino)ethoxy]bromobenzene, there is obtained 1 {p [2-(1 methyl 4 piperazino)et1hoxy]- p heny1}-2-phenyl-6-methoXy-3,4-dihydronaphthalene and the hydrochloride thereof.
EXAMPLE 15 l-[p (2-hexamethyleneim-in0elhoxy)phenyl] -2-phenyl-6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p 2-diethylaminoethoxy) bromobenzene by p-(2- hexamethyleneiminoethoxy)bromobenzene, there is obtained 1 [p (2 hexamethyleneiminoethoxy)phenyl]-2- phenyl-6-methoxy-3,4-dihydronaphthalene and the hydrochloride thereof.
EXAMPLE 16 1 [p- (Z-homopiperazinoethoxy phenyl] -2-phenyl-6-methoxy 3,4 dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-diethylaminoethoxy)bromobenzene by p-(2- homopiperazinoethoxy)bromobenzene, there is obtained 1 -[p-(Z homopiperazinoethoxy) phenyl]-2-phenyl-6-methoxy-3,4-dihydronaphthalene and the hydrochloride there of.
EXAMPLE 17 1 [p (2-homom0rpholinoethoxy)phenyl] 2 phenyl-6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof Using the procedure described in Example 1, but replacing p-(2-diethylaminoethoxy)-bromobenzene by p-(2- homomorpholinoethoxy)bromobenzene, there is obtained 1 [p (2 homomorpholinoethoxy)phenyl] 2-phenyl-6- methoxy-3,4-dihydronaphthalene and the hydrochloride thereof.
EXAMPLE 18 1 [p- (Z-diethylaminoethoxy )phenyl] -2-phenyl-6-methoxy- 3,4-dihydronaphthalene methiodide A solution of 1 g. of 1-[p-(Z-diethylaminoethoxy)phenyl]-2-phenyl-6-methoxy-3,4-dihydronaphthalene in 12 ml. of acetonitrile is cooled in ice. To the cooled solution is added 1.5 ml. of methyl iodide and the mixture is allowed to stand overnight before being poured into 100 ml. of ether. The solid which separates is isolated by filtration and recrystallized from a mixture of ethyl acetate and ether. There is thus obtained 1-[p-(2-diethylaminoeth- -oxy)pheny1] 2 phenyl 6-methoxy-3,4-dihydronaphthalene methiodide in the form of a crystalline solid.
Similarly, using the above procedure, but replacing methyl iodide by ethyl bromide, propyl bromide, allyl bromide, and benzyl bromide, there are obtained the ethobromide, propyl bromide, allyl bromide, and benzyl bromide, respectively, of 1-[p-(2-diethylaminoethoxy) phenyl -2-phenyl-6-methoXy-3 ,4-dihydronaphthalene.
Similarly, using the procedure described in Example 18, but replacing 1-[p-(Z-diethylaminoethoxy)phenyl]-2- phenyl-6-methoxy-3,4-dihydronaphthalene by any of the free bases prepared as described in Examples 2 to 17, inclusive, there are prepared the corresponding methiodides and like quaternary ammonium salts.
EXAMPLE 19 1 [p-(2 diethylaminoethoxy)phenyl]-2-phenyl-6-methoxy-3,4-dihydronaphthalene N-oxide and the hydrochloride thereof To a solution of 1-[p-(Z-diethyIaminoeth-oxy)phenyl]-2- phenyl-6-methoxy-3,4-dihydronaphthalene in 50 ml. of absolute ethanol is added an equimolar quantity of 30% hydrogen peroxide. The mixture is allowed to stand for 4 days at room temperature, at the end of which time the mixture is shaken with 0.5 g. of platinum oxide until a test for peroxide is negative. The mixture is then filtered and the filtrate is evaporated to dryness under reduced pressure. The residue is recrystallized from a mixture of chloroform and ethyl acetate. There is thus obtained 1 [p (2-diethylaminoethoxy)phenyl]-2-phenyl-6-methoxy-3,4-dihydronaphthalene N-oxide.
The N-oxide so obtained is converted to the corresponding hydrochloride by dissolving the N-oxide in ether and treating the ether solution with an excess of a saturated solution of hydrogen chloride in ether. The solid which separates is isolated by filtration. There is thus obtained 1- [p- Z-diethylaminoethoxy) phenyl] -2-phenyl-6- methoxy-3,4-dihydronaphthalene N-oxide hydrochloride.
Using the above procedure, but replacing 1-[p-(2-diethylaminoethoxy)phenyl] 2 phenyl-6-methoxy-3,4-dihydronaphthalene by any of the free bases prepared as described in Examples 2 to 17, inclusive, there are obtained the corresponding N-oxides and the hydrochlorides thereof.
EXAMPLE 20 ride 1250 Dicalcium phosphate 2500 Methylcellul-ose, U.S.P. (15 cps.) 65 Talc, bolted 450 Calcium stearate, fine powder 35 The powdered 1-[p-Z-diethylaminoethoxy)phenyl]-2- phenyl-6-methoxy-3,4-dihydronaphth-alene hydrochloride and the calcium phosphate are mixed Well and granulated with a 7.5% aqueous solution of the methylcellulose. The granules are passed through a No. 8 screen and dried carefully at F. The dried granules are passed through a No. 12 screen, mixed thoroughly with the talc and calcium stearate, and compressed into tablets.
To produce tablets containing 250 mg. of active ingredient the amount of the latter employed in the above formulation is increased to 2500 g.
I claim:
1. A compound selected from the class consisting of (a) compounds having the formula:
wherein R and R are selected from the class consisting of lower-alkyl from 1 to 8 carbon atoms, inclusive, and together with the nitrogen atom, a member selected from :the class consisting of pyrrolidino, Z-methylpyrrolidino, 2,2-dimethylpyrrolidino, piperazino, 4-methy1piperazino, 2,4-dimethylpiperazino, morpholino, piperidino, Z-methylpiperidino, 3-methylpiperidino, hexamethyleneimino, homopiperazino and homomorpholino, C H represents alkylene from 2 to 6 carbon atoms, inclusive, alkoxy has from 1 to 8 carbon atoms, inclusive, and x is an integer from 1 to 4, inclusive;
(b) the nontoxic pharmacologically acceptable acid addition salts of compounds of the above formula;
(c) the N-oxides of compounds of the above formula;
((1) the nontoxic pharmacologically acceptable acid addition salts of N-oxides of compounds of the above formula; and
(e) quaternary ammonium salts of compounds of the above formula, selected from the class consisting of lower-alkyl quaternary ammonium halides, loweralkenyl quaternary ammonium halides, lower-alkyl quaternary ammonium sulfates, aralkyl quaternary ammonium halides, and lower-alkyl quaternary arylsulfonates.
2. 1 [p- (Z-diethylaminoethoxy)phenyl]-2-phenyl-6- methoxy-3,4-dihydronaphthalene.
3. 1 [p (2-diethylaminoethoxy)phenyl] -2-phenyl-6- methoxy-3,4-dihydronaphthalene hydrochloride.
4. l [p (2 pyrrolidinoethoxy)phenyl] 2-phenyl-6- m'ethoxy-3,4dihydronaphthalene.
5. 1 [p (2 pyrrolidinoethoxy)phenyl] 2-phenyl-6- methoxy-3,4-dihydronaphthalene hydrochloride.
alkoxy 4 wherein R and R are selected from the class consisting of lower-alkyl from 1 to 8 carbon atoms, inclusive, and together with the nitrogen atom, a member selected from the class consisting of pyrrolidino, Z-methylpyrrolidino, 2,2-dimethylpyrrolidino, piperazino, 4-methylpiperazino, 2,4-dimethylpiperazino, m'orpholino, piperidino, Z-methylpiperidino, 3-methylpiperidino, hexamethyleneimino, homopiperazino and homomorpholino, C H represents alkylene from 2 to 6 carbon atoms, inclusive, and alkoxy has from 1 to 8 carbon atoms, inclusive;
(b) the nontoxic pharmacologically acceptable acid addition salts of compounds of the above formula;
(0) the N-oxides of compounds of the above formula;
(d) the nontoxic pharmacologically acceptable acid addition salts of N-oxides of compounds of the above formula; and
(e) quaternary ammonium salts of compounds of the above formula, selected from the class consisting of lower-alkyl quaternary ammonium halides, loweralkenyl quaternary ammonium halides, loWer-alkyl quaternary ammonium sulfates, aralkyl quaternary ammonium halides, and lower-alkyl quaternary arylsulfonates.
7. A nontoxic pharmacologically acceptable acid addition salt of 1-[p-(2-diethylaminoethoxy)phenyl]-2-phenyl-6-methoxy-3,4-dihydronaphthalene.
8. A nontoxic pharmacologically acceptable acid addition salt of 1-[p-(2-pyrrolidinoethoxy)phenyl] -2-phenyl- 6-methoxy-3,4-dihydronaphthalene.
References Cited by the Examiner UNITED STATES PATENTS 1,915,334 6/1933 Salzberg et a1. 260-243 2,075,359 3/ 1937 Salzberg et a1 167-22 2,187,719 1/ 1940 Williams 260239 2,425,320 8/1947 Hill 252-149 2,606,155 8/1952 Hill '252149 2,623,839 12/1952 Taub 16758 2,752,284 6/1956 Berliner et a1. 167-58 3,076,816 2/1963 Miller 260326.5
, ALEX MAZEL, Primary Examiner.
IRVING MARCUS, Examiner. JOSE TOVAR, Assistant Examiner.

Claims (1)

1. A COMPOUND SELECTED FROM THE CLASS CONSISTING OF (A) COMPOUNDS HAVING THE FORMULA:
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