1-(3-CHLORO-4-CYCLOALKYLPHENYL)-CYCLO-ALKYL-1-CARBOXYLIC ACIDS

1277239 1- Phenyl - cycloalkane - 1 - carboxylic acids;. TAKEDA YAKUHIN KOGYO KK 4 July 1969 [4 July 1968 13 July 1969 18 Jan 1969] 33732/69 Heading C2C Novel 1 - phenyl - cycloalkane - 1 - carboxylic acids of the general formula wherein X is a hydrogen or halogen atom, R is a C 3-6 alkyl or cycloal...

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Hauptverfasser: KISHIMOTO S,JA, MINAMIDA I,JA, NOGUCHI S,JA, KAWAI K,JA, OBAYASHI M,JA
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MINAMIDA I,JA
NOGUCHI S,JA
KAWAI K,JA
OBAYASHI M,JA
description 1277239 1- Phenyl - cycloalkane - 1 - carboxylic acids;. TAKEDA YAKUHIN KOGYO KK 4 July 1969 [4 July 1968 13 July 1969 18 Jan 1969] 33732/69 Heading C2C Novel 1 - phenyl - cycloalkane - 1 - carboxylic acids of the general formula wherein X is a hydrogen or halogen atom, R is a C 3-6 alkyl or cycloalkyl group and n is an integer of from 2 to 5, and pharmaceutically acceptable salts or derivatives thereof derived by conversion of the carboxylic group, i.e. acid amides and esters and hydroxamic acids, are prepared (a) by reaction of a phenyl-acetonitrile of the. general formulawith an alkylene halide of the general; formula X1(CH 2 ) n X1, wherein X1 is a halogen atom, followed optionally by halogenation and/or hydrolysis. of the resulting 1-phenyl-cycloalkane-1-nitrile of the general formula (b)- byhalogenation of a phenyl'-acetonitrile of the second general. formula above and reaction of the resulting-phenyl-acetonitrile of the.general formula wherein X11 is a halogen atom, with an alkylene halide of the third general formula above, followed optionally by hydrolysis of the resulting 1-phenyl-cycloalkane-1-nitrile of the general formula and (c) when n is 2 ,by reaction of diazomethane with, an α-phenyl-acrylic acid of the general formula. or a pharmaceutically acceptable salt or deriva; tive thereof derived by conversion of the carboxylic group and denitrification of the resultting 3 - phenyl - 1 - pyrazoline - 3 - carboxylic acid of the general formula or pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group, followed optionally by conversion of a resulting 1-phenyl-cycloalkane-1,-carboxylic acid of the first general formula above to a pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group (other than a nitrile in the case of (a) and (b) above), or by conversion of a resulting pharmaceutically acceptable salt or derivative of a 1-phenyl-cycloalkane- 1 -carboxylic acid of the first general, formula above derived by conversion of the carboxylic group to the free acid. Pharmaceutical compositions having antiinflammatory activity comprise, as active ingredient, a 1-phenylcycloalkane-carboxylic acid of the first general formula above or a pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group, in admixture with a pharmaceutically acceptable carrier or adjuvant, and may be administered orally or by way of injection.
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TAKEDA YAKUHIN KOGYO KK 4 July 1969 [4 July 1968 13 July 1969 18 Jan 1969] 33732/69 Heading C2C Novel 1 - phenyl - cycloalkane - 1 - carboxylic acids of the general formula wherein X is a hydrogen or halogen atom, R is a C 3-6 alkyl or cycloalkyl group and n is an integer of from 2 to 5, and pharmaceutically acceptable salts or derivatives thereof derived by conversion of the carboxylic group, i.e. acid amides and esters and hydroxamic acids, are prepared (a) by reaction of a phenyl-acetonitrile of the. general formulawith an alkylene halide of the general; formula X1(CH 2 ) n X1, wherein X1 is a halogen atom, followed optionally by halogenation and/or hydrolysis. of the resulting 1-phenyl-cycloalkane-1-nitrile of the general formula (b)- byhalogenation of a phenyl'-acetonitrile of the second general. formula above and reaction of the resulting-phenyl-acetonitrile of the.general formula wherein X11 is a halogen atom, with an alkylene halide of the third general formula above, followed optionally by hydrolysis of the resulting 1-phenyl-cycloalkane-1-nitrile of the general formula and (c) when n is 2 ,by reaction of diazomethane with, an α-phenyl-acrylic acid of the general formula. or a pharmaceutically acceptable salt or deriva; tive thereof derived by conversion of the carboxylic group and denitrification of the resultting 3 - phenyl - 1 - pyrazoline - 3 - carboxylic acid of the general formula or pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group, followed optionally by conversion of a resulting 1-phenyl-cycloalkane-1,-carboxylic acid of the first general formula above to a pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group (other than a nitrile in the case of (a) and (b) above), or by conversion of a resulting pharmaceutically acceptable salt or derivative of a 1-phenyl-cycloalkane- 1 -carboxylic acid of the first general, formula above derived by conversion of the carboxylic group to the free acid. 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TAKEDA YAKUHIN KOGYO KK 4 July 1969 [4 July 1968 13 July 1969 18 Jan 1969] 33732/69 Heading C2C Novel 1 - phenyl - cycloalkane - 1 - carboxylic acids of the general formula wherein X is a hydrogen or halogen atom, R is a C 3-6 alkyl or cycloalkyl group and n is an integer of from 2 to 5, and pharmaceutically acceptable salts or derivatives thereof derived by conversion of the carboxylic group, i.e. acid amides and esters and hydroxamic acids, are prepared (a) by reaction of a phenyl-acetonitrile of the. general formulawith an alkylene halide of the general; formula X1(CH 2 ) n X1, wherein X1 is a halogen atom, followed optionally by halogenation and/or hydrolysis. of the resulting 1-phenyl-cycloalkane-1-nitrile of the general formula (b)- byhalogenation of a phenyl'-acetonitrile of the second general. formula above and reaction of the resulting-phenyl-acetonitrile of the.general formula wherein X11 is a halogen atom, with an alkylene halide of the third general formula above, followed optionally by hydrolysis of the resulting 1-phenyl-cycloalkane-1-nitrile of the general formula and (c) when n is 2 ,by reaction of diazomethane with, an α-phenyl-acrylic acid of the general formula. or a pharmaceutically acceptable salt or deriva; tive thereof derived by conversion of the carboxylic group and denitrification of the resultting 3 - phenyl - 1 - pyrazoline - 3 - carboxylic acid of the general formula or pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group, followed optionally by conversion of a resulting 1-phenyl-cycloalkane-1,-carboxylic acid of the first general formula above to a pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group (other than a nitrile in the case of (a) and (b) above), or by conversion of a resulting pharmaceutically acceptable salt or derivative of a 1-phenyl-cycloalkane- 1 -carboxylic acid of the first general, formula above derived by conversion of the carboxylic group to the free acid. 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TAKEDA YAKUHIN KOGYO KK 4 July 1969 [4 July 1968 13 July 1969 18 Jan 1969] 33732/69 Heading C2C Novel 1 - phenyl - cycloalkane - 1 - carboxylic acids of the general formula wherein X is a hydrogen or halogen atom, R is a C 3-6 alkyl or cycloalkyl group and n is an integer of from 2 to 5, and pharmaceutically acceptable salts or derivatives thereof derived by conversion of the carboxylic group, i.e. acid amides and esters and hydroxamic acids, are prepared (a) by reaction of a phenyl-acetonitrile of the. general formulawith an alkylene halide of the general; formula X1(CH 2 ) n X1, wherein X1 is a halogen atom, followed optionally by halogenation and/or hydrolysis. of the resulting 1-phenyl-cycloalkane-1-nitrile of the general formula (b)- byhalogenation of a phenyl'-acetonitrile of the second general. formula above and reaction of the resulting-phenyl-acetonitrile of the.general formula wherein X11 is a halogen atom, with an alkylene halide of the third general formula above, followed optionally by hydrolysis of the resulting 1-phenyl-cycloalkane-1-nitrile of the general formula and (c) when n is 2 ,by reaction of diazomethane with, an α-phenyl-acrylic acid of the general formula. or a pharmaceutically acceptable salt or deriva; tive thereof derived by conversion of the carboxylic group and denitrification of the resultting 3 - phenyl - 1 - pyrazoline - 3 - carboxylic acid of the general formula or pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group, followed optionally by conversion of a resulting 1-phenyl-cycloalkane-1,-carboxylic acid of the first general formula above to a pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group (other than a nitrile in the case of (a) and (b) above), or by conversion of a resulting pharmaceutically acceptable salt or derivative of a 1-phenyl-cycloalkane- 1 -carboxylic acid of the first general, formula above derived by conversion of the carboxylic group to the free acid. Pharmaceutical compositions having antiinflammatory activity comprise, as active ingredient, a 1-phenylcycloalkane-carboxylic acid of the first general formula above or a pharmaceutically acceptable salt or derivative thereof derived by conversion of the carboxylic group, in admixture with a pharmaceutically acceptable carrier or adjuvant, and may be administered orally or by way of injection.</abstract><oa>free_for_read</oa></addata></record>
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subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PERFORMING OPERATIONS
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
TRANSPORTING
VEHICLES IN GENERAL
VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISEPROVIDED FOR
title 1-(3-CHLORO-4-CYCLOALKYLPHENYL)-CYCLO-ALKYL-1-CARBOXYLIC ACIDS
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