4994456 pyridinecarboxylic acid amide derivatives and pharmaceutical compositions comprising same

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viii New Patents 4994456 4994471 PYRIDINECARBOXYLIC ACID AMIDE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS COMPRISING SAME Katsutosh Miura, Hiroyasu Koyama, Toshiji Sugai, Hiroaki Yamada, Einosuk Sakurai, Masato Horigome, Saitama, Japan assigned to Nisshin Flour Milling Co Ltd Compounds are disclosed of the formula See Pa- tent for Chemical Structure (I) wherein R1 is hydrogen; C1-C6 alkyl; C3-C6 cycloalkyl or diphenylmethyl; Y is -NH(CH2)n-R2 or See Pa- tent for Chemical Structure R2 is OH or -ONO2; 1 is 2 or 3; m is 0 or 1; and n is 2 to 8; and phys- iologically acceptable acid addition salts thereof. The compounds of formula (I) are of a blood flow-increasing and hypotensive actions and can be used for the therapy or prevention of diseases in the cardiovascular system. 4994470 BENZOPYRAN DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM Michel Barreau, Jean-Claude Hardy, Christian Renault, Montgeron, France assigned to Rhone- Poulenc Sante New benzopyran derivatives of general formula (I) in which: R1 denotes a hydrogen or halogen atom or a hydroxy, alkyloxy, nitro, amino, alkylsulphonamido, bis(alkylsulphonyl)amino, or acylamino radical, R denotes a radical of general formula: See Patent for Chemical Struc- ture in which A denotes a single bond or a methy- lene radical and R2 and R3 which may be identical or different, denote a hydrogen or halogen atom or a hydroxy, alkyl, alkyloxy, nitro, amino, alkylsulphonamido, bi- s(alkylsulphonyl)amino, acylamino, sulphamoyl or cyano radical, or form together, when they are adjacent, a methylenedioxy or ethylenedioxy radical, or alternatively R denotes a 2-oxo-2H- benzimidazolyl radical, and R' and R" are iden- tical and denote hydrogen atoms or alkyl radicals, their isomeric forms and their prepara- tion. These new products are useful as anti- arrhythmic and antifibrillating agents. See Patent for Chemical Structure (I) N-ARYL-N-(1 SUBSTITUTED-3 ALKOXY-4 PIPERIDINYL)AMIDES AND PHARMACEUTICAL COMPOSITIONS AND METHODS EMPLOYING SUCH COMPOUNDS Nhora L Lalinde, Joh Moliterni, H Kenneth Spencer assigned to BOC Inc This invention pertains to novel N-aryl-N-(N- substituted 3-alkoxy-4-piperidinyl)amides use- ful as analgesics, and methods of administering analgesia, which comprises the systemic ad- ministration to mammals of such compounds, and pharmaceutical compositions containing such compounds, wherein the novel compounds have the general formula: See Patent for Chem- ical Structure (I) including optically active isomeric forms, cis/trans isomeric forms and the pharmaceutically acceptable acid addition salts therof, wherein: R is an aryl group selected from the group consisting of phenyl and substituted phenyl, wherein the substituents on the phenyl group are independently selected from the group consisting of halogen, lower-alkyl, lower- alkoxy, and combinations thereof; R1 is an alkyl group selected from the group consisting of lower-alkyl, lower-alkenyl, and lower-alkoxy lower-alkyl, each alkyl group having from 1 to 6 carbon atoms; R2 is a member selected from the group consisting of phenyl lower-alkyl, thienyl lower-alkyl, pyrazolyl lower-alkyl, tetrazolyl lower-alkyl, 4, 5-dihydro-5-oxo-lH-tetrazolyl lower-alkyl, 1,3-dihydro-l, 3-dioxo-2H- isoindolyl lower-alkyl, and 2, 3-dihydro-2-oxol H-benzimidazolyl lower-alkyl; and R3 is a mem- ber selected from the group consisting of hydro- gen, lower-alkyl and lower-alkyl aryl. 4994493 N-SUBSTITUTED 5- NITROANTHRANILIC ACIDS, A PROCESS FOR THEIR PREPARATION, THEIR USE, AND PHARMACEUTICAL PRODUCTS BASED ON THESE COMPOUNDS Raine Greger, Heinrich C Englert, Hans-Jochen Lang, Max Hropot, Heitersheim, Federal Republic Of Germany assigned to Max-Planck- Gesellschaft zur Forderung der Wissenschaften; Hoechst Aktiengesellscha

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Page 1: 4994456 Pyridinecarboxylic acid amide derivatives and pharmaceutical compositions comprising same

viii New Patents

4994456 4994471

P Y R I D I N E C A R B O X Y L I C A C I D A M I D E D E R I V A T I V E S A N D

P H A R M A C E U T I C A L C O M P O S I T I O N S C O M P R I S I N G

S A M E

Katsutosh Miura, Hiroyasu Koyama, Toshiji Sugai, Hiroaki Yamada, Einosuk Sakurai, Masato Horigome, Saitama, Japan assigned to Nisshin Flour Milling Co Ltd

Compounds are disclosed of the formula See Pa- tent for Chemical Structure (I) wherein R1 is hydrogen; C1-C6 alkyl; C3-C6 cycloalkyl or diphenylmethyl; Y is -NH(CH2)n-R2 or See Pa- tent for Chemical Structure R2 is OH or -ONO2; 1 is 2 or 3; m is 0 or 1; and n is 2 to 8; and phys- iologically acceptable acid addition salts thereof. The compounds of formula (I) are of a blood flow-increasing and hypotensive actions and can be used for the therapy or prevention of diseases in the cardiovascular system.

4994470

B E N Z O P Y R A N D E R I V A T I V E S A N D P H A R M A C E U T I C A L

C O M P O S I T I O N S C O N T A I N I N G T H E M

Michel Barreau, Jean-Claude Hardy, Christian Renault, Montgeron, France assigned to Rhone- Poulenc Sante

New benzopyran derivatives of general formula (I) in which: R1 denotes a hydrogen or halogen atom or a hydroxy, alkyloxy, nitro, amino, alkylsulphonamido, bis(alkylsulphonyl)amino, or acylamino radical, R denotes a radical of general formula: See Patent for Chemical Struc- ture in which A denotes a single bond or a methy- lene radical and R2 and R3 which may be identical or different, denote a hydrogen or halogen atom or a hydroxy, alkyl, alkyloxy, nitro, amino, alkylsulphonamido, bi- s(alkylsulphonyl)amino, acylamino, sulphamoyl or cyano radical, or form together, when they are adjacent, a methylenedioxy or ethylenedioxy radical, or alternatively R denotes a 2-oxo-2H- benzimidazolyl radical, and R' and R" are iden- tical and denote hydrogen atoms or alkyl radicals, their isomeric forms and their prepara- tion. These new products are useful as anti- arrhythmic and antifibrillating agents. See Patent for Chemical Structure (I)

N - A R Y L - N - ( 1 S U B S T I T U T E D - 3 A L K O X Y - 4 P I P E R I D I N Y L ) A M I D E S

A N D P H A R M A C E U T I C A L C O M P O S I T I O N S A N D M E T H O D S

E M P L O Y I N G S U C H C O M P O U N D S

Nhora L Lalinde, Joh Moliterni, H Kenneth Spencer assigned to BOC Inc

This invention pertains to novel N-aryl-N-(N- substituted 3-alkoxy-4-piperidinyl)amides use- ful as analgesics, and methods of administering analgesia, which comprises the systemic ad- ministration to mammals of such compounds, and pharmaceutical compositions containing such compounds, wherein the novel compounds have the general formula: See Patent for Chem- ical Structure (I) including optically active isomeric forms, cis/trans isomeric forms and the pharmaceutically acceptable acid addition salts therof, wherein: R is an aryl group selected from the group consisting of phenyl and substituted phenyl, wherein the substituents on the phenyl group are independently selected from the group consisting of halogen, lower-alkyl, lower- alkoxy, and combinations thereof; R1 is an alkyl group selected from the group consisting of lower-alkyl, lower-alkenyl, and lower-alkoxy lower-alkyl, each alkyl group having from 1 to 6 carbon atoms; R2 is a member selected from the group consisting of phenyl lower-alkyl, thienyl lower-alkyl, pyrazolyl lower-alkyl, tetrazolyl lower-alkyl, 4, 5-dihydro-5-oxo-lH-tetrazolyl lower-alkyl, 1,3-dihydro-l, 3-dioxo-2H- isoindolyl lower-alkyl, and 2, 3-dihydro-2-oxol H-benzimidazolyl lower-alkyl; and R3 is a mem- ber selected from the group consisting of hydro- gen, lower-alkyl and lower-alkyl aryl.

4994493

N - S U B S T I T U T E D 5- N I T R O A N T H R A N I L I C A C I D S , A

P R O C E S S F O R T H E I R P R E P A R A T I O N , T H E I R U S E , A N D P H A R M A C E U T I C A L P R O D U C T S B A S E D O N T H E S E C O M P O U N D S

Raine Greger, Heinrich C Englert, Hans-Jochen Lang, Max Hropot, Heitersheim, Federal Republic Of Germany assigned to Max-Planck- Gesellschaft zur Forderung der Wissenschaften; Hoechst Aktiengesellscha