Claims for Patent: 3,998,966

Summary for Patent: 3,998,966

Title:	Anti-inflammatory, analgesic, anti-pyretic and anti-pruritic 6-substituted 2-naphthyl acetic acid derivative-containing compositions and methods of use thereof
Abstract:	2-Naphthyl acetic acid derivatives and the corresponding amides, esters, hydroxamic acids and addition salts thereof, optionally substituted at the .alpha.-position on the acetic acid moiety and/or at position 6 and/or at positions 1, 4, 7 or 8 on the naphthyl ring and optionally saturated at positions 3 and 4, are anti-inflammatory, analgesic, anti-pyretic and anti-pruritic agents. A pharmaceutical method of effecting treatment of inflammation, pain, pyrexia and pruritus by the administration of naphthyl acetic acid derivatives. A pharmaceutical composition for use in the treatment of the above maladies comprising a naphthyl acetic acid derivative.
Inventor(s):	Fried; John H. (Palo Alto, CA), Harrison; Ian T. (Palo Alto, CA)
Assignee:	Syntex Corporation (Panama, PM)
Application Number:	05/558,988
Patent Claims:	1. A composition for treating inflammation, pain, pyrexia and pruritus in mammals which comprises a pharmaceutically acceptable non-toxic excipient and a therapeutically effective amount of a compound represented by the formula: ##STR9## where: R.sup.7 is alkyl having 1 to 6 carbon atoms, cycloalkyl having 3 to 7 carbon atoms, hydroxymethyl, alkoxymethyl having 2 to 7 carbon atoms, trifluoromethyl, vinyl, ethynyl, fluoro, chloro, hydroxy or a conventional hydrolyzable ester thereof derived from a hydrocarbon carboxylic acid having 1 to 12 carbon atoms, alkoxy having 1 to 6 carbon atoms, difluoromethoxy, alkoxymethyloxy, having 2 to 7 carbon atoms, alkylthiomethyloxy having 2 to 7 carbon atoms, alkylthio having 1 to 6 carbon atoms, difluoromethylthio, alkoxymethylthio having 2 to 7 carbon atoms, alkylthiomethylthio having 2 to 7 carbon atoms, formyl, carboxy, alkoxycarbonyl having 2 to 7 carbon atoms, acetyl, cyano or phenyl optionally p-monosubstituted with methyl, fluoro, chloro, hydroxy, methoxy or ethyl; one of R.sup.10 and R.sup.11 is hydrogen, and the other is methyl, ethyl, difluoromethyl, fluoro or chloro, or R.sup.10 and R.sup.11 taken together are alkylidene, halomethylene or ethylene; an alkyl ester of a compound of formula XIV derived from an alkanol having 1 to 12 carbon atoms; or a pharmaceutically acceptable addition salt thereof. 2. The composition according to claim 1 wherein said compound is 6-methoxy-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 3. The composition according to claim 1 wherein said compound is 6-methoxy-2-naphthyl-.alpha.-methylacetic acid. 4. The composition according to claim 1 wherein said compound is d 6-methoxy-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 5. The composition according to claim 1 wherein said compound is d 6-methoxy-2-naphthyl-.alpha.-methylacetic acid. 6. The composition according to claim 1 wherein said compound is 6-methylthio-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 7. The composition according to claim 1 wherein said compound is 6-methylthio-2-naphthyl-.alpha.-methylacetic acid. 8. The composition of claim 1 wherein said compound is the sodium salt of 6-methoxy-2-naphthyl-.alpha.-methylacetic acid. 9. The composition of claim 1 wherein said compound is the sodium salt of d 6-methoxy-2-naphthyl-.alpha.-methylacetic acid. 10. The composition of claim 1 wherein said compound is methyl-6-methoxy-2-naphthyl-.alpha.-methylacetate. 11. A method for treating inflammation, pain, pyrexia and pruritus in mammals which comprises administering to a mammal suffering therefrom a therapeutically effective amount of a compound represented by the formula: ##STR10## where: R.sup.7 is alkyl having 1 to 6 carbon atoms, cycloalkyl having 3 to 7 carbon atoms, hydroxymethyl, alkoxymethyl having 2 to 7 carbon atoms, trifluoromethyl, vinyl, ethynyl, fluoro, chloro, hydroxy or a conventional hydrolyzable ester thereof derived from a hydrocarbon carboxylic acid having 1 to 12 carbon atoms, alkoxy having 1 to 6 carbon atoms, difluoromethoxy, alkoxymethyloxy having 2 to 7 carbon atoms, alkylthiomethyloxy having 2 to 7 carbon atoms, alkylthio having 1 to 6 carbon atoms, difluoromethylthio, alkoxymethylthio having 2 to 7 carbon atoms, alkylthiomethylthio having 2 to 7 carbon atoms, formyl, carboxy, alkoxycarbonyl having 2 to 7 carbon atoms, acetyl, cyano or phenyl optionally p-monosubstituted with methyl, fluoro, chloro, hydroxy, methoxy or ethyl; one of R.sup.10 and R.sup.11 is hydrogen, and the other is methyl, ethyl, difluoromethyl, fluoro or chloro, or R.sup.10 and R.sup.11 taken together are alkylidene, halomethylene or ethylene; an alkyl ester of a compound of formula XIV derived from an alkanol having 1 to 12 carbon atoms; or a pharmaceutically acceptable addition salt thereof. 12. The method according to claim 11 wherein said compound is 6-methoxy-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 13. The method according to claim 11 wherein said compound is 6-methoxy-2-naphthyl-.alpha.-methylacetic acid. 14. The method according to claim 11 wherein said compound is 6-methylthio-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 15. The method according to claim 11 wherein said compound is 6-methylthio-2-naphthyl-.alpha.-methylacetic acid. 16. The method according to claim 11 wherein said compound is d 6-methoxy-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 17. The method according to claim 11 wherein said compound is d 6-methoxy-2-naphthyl-.alpha.-methylacetic acid. 18. The method according to claim 11 wherein said compound is 6-fluoro-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 19. The method according to claim 11 wherein said compound is 6-chloro-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 20. The method according to claim 11 wherein said compound is 6-methyl-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 21. The method according to claim 11 wherein said compound is 6-trifluoromethyl-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 22. The method according to claim 11 wherein said compound is 6-difluoromethoxy-2-naphthyl-.alpha.-methylacetic acid, an alkyl ester thereof derived from an alkanol having 1 to 12 carbon atoms, or a pharmaceutically acceptable addition salt thereof. 23. The method of claim 11 wherein said compound is the sodium salt of 6-methoxy-2-naphthyl-.alpha.-methylacetic acid. 24. The method of claim 11 wherein said compound is the sodium salt of d 6-methoxy-2-naphthyl-.alpha.-methylacetic acid. 25. The method of claim 11 wherein said compound is methyl 6-methoxy-2-naphthyl-.alpha.-methylacetate.