首页> 外国专利> Sulfonamidsubstituerte benzopyranderivater, fremgangsmÕter for deres fremstilling, deres anvendelse som medikament samt farmas°ytiske preparater inneholdende forbindelsene

Sulfonamidsubstituerte benzopyranderivater, fremgangsmÕter for deres fremstilling, deres anvendelse som medikament samt farmas°ytiske preparater inneholdende forbindelsene

机译:磺酰胺取代的苯并吡喃衍生物,其制备方法,其在含有该化合物的药物和药物制剂中的用途

摘要

4-Sulphonamido-benzopyran derivatives (I) are new. 4-Sulphonamido-benzopyran derivatives of formula (I) and their salts are new: R1, R2 = H, CF3, C2F5, C3F7, alkyl, or phenyl optionally mono- or disubstituted; or R1 + R2 = alkylene; R3 = R10-Cn-H2n-N(R11)- or R10-CnH2n- in which 1 CH2 is optionally replaced; R4 = R13-CrH2r in which 1 CH2 is optionally replaced; or R3 + R4 = alkylene with 1 CH2 optionally replaced; n = 1-10; r = 1-20; R10 = H, Me, cycloalkyl, CF3, C2F5, or C3F7; R11 = H or alkyl; or R10 + R11 = a bond when n is at least 3; R13 = Me, CF3, C2F5, C3F7, cycloalkyl, NR15R16, or phenyl or N-containing heterocyclyl (both optionally mono- or disubstituted); R15, R16 = tetra- or pentamethylene in which 1 CH2 is optionally replaced); R5 = Y-CsH2s-R 18 or phenyl (optionally mono- or disubstituted); Y = O, S or NR10c; R10c = H or alkyl; s = 1-8; R18 = H, CF3, C2F5, C3F7, cycloalkyl, COOR21, NR15aR16a, N-containing heterocyclyl, or phenyl or thienyl (both optionally mono- or disubstituted); or R15a + R16a = tetra- or pentamethylene in which 1 CH2 is optionally replaced); R21 = H or alkyl; R6 = OR10d or OCOR10d B = H; or R6 + B = a bond; R10d = H or alkyl. The full definitions are given in the DEFINITIONS (Full Definitions) Field. Independent claims are also included for: (1) preparation of (I); (2) pharmaceutical compositions containing (I) and a beta-blocker.
机译:4-磺酰胺基-苯并吡喃衍生物(I)是新的。式(I)的4-磺酰胺基-苯并吡喃衍生物及其盐是新的:R 1,R 2 = H,CF 3,C 2 F 5,C 3 F 7,烷基或苯基,其任选被单取代或二取代;或R 1 + R 2 =亚烷基;或R 3 = R 10 -C n -H 2n -N(R 11)-或R 10 -C n H 2n-,其中1个CH 2任选被取代; R 4 = R 13 -CrH 2r,其中1个CH 2被任选地取代;或R 3 + R 4 =亚烷基,其中1个CH 2任选取代; n = 1-10; r = 1-20; R 10 = H,Me,环烷基,CF 3,C 2 F 5或C 3 F 7; R 11 = H或烷基;或R 10 + R 11 = n为3以上时的键。 R 13 = Me,CF 3,C 2 F 5,C 3 F 7,环烷基,NR 15 R 16或苯基或含N的杂环基(任选被单或双取代); R 15,R 16 =四亚甲基或五亚甲基,其中1个CH 2任选地被取代); R 5 = Y-CsH 2s -R 18或苯基(任选被单或双取代); Y = O,S或NR 1 0c; R10c = H或烷基; s = 1-8; R 18 = H,CF 3,C 2 F 5,C 3 F 7,环烷基,COOR 21,NR15aR16a,含氮杂环基或苯基或噻吩基(两者任选被单或双取代);或R15a + R16a =四亚甲基或五亚甲基,其中1个CH2可任选取代);或R 21 = H或烷基; R 6 = OR10d或OCOR10d B = H;或R 6 + B =键;或R 10d = H或烷基。完整定义在“定义(完整定义)”字段中给出。还包括以下方面的独立权利要求:(1)(I)的制备; (2)包含(I)和β-阻断剂的药物组合物。

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