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1-ARYLSULPHONYL-3-PHENYL-1,4,5,6-TETRAHYDROPYRIDAZINES

机译:1-芳基磺酰基-3-苯基-1,4,5,6-四氢哒嗪

摘要

PCT No. PCT/US93/06394 Sec. 371 Date Mar. 6, 1995 Sec. 102(e) Date Mar. 6, 1995 PCT Filed Jul. 1, 1993 PCT Pub. No. WO94/01412 PCT Pub. Date Jan. 20, 1994Disclosed are progestin agonists having the following formula: IMAGE wherein: A is IMAGE W is absent or -CH=CH-; R1 are independently selected from the group consisting of halogen, -CF3, and NO2, or both R1 may be joined to form a bi-radical which is -CH=CHCH=CH-; R3 are independently selected from the group consisting of hydrogen, C1-6 branched or linear alkyl, halogen and -CF3, with the proviso that R3 at the 3-position must be H where R3 at the 4-position is H, or both R3 may be joined to form a bi-radical selected from the group consisting of -CH=CHCH=CH-, -C(NC1-4alkyl2)=CHCH=CH- and -(CH2)4-; R5 is selected from the group consisting of H and Me; with the proviso that only one of R1 and R3 forms the fused bi-radical; and the stereoisomers.
机译:PCT号PCT / US93 / 06394秒371日期1995年3月6日第102(e)日期1995年3月6日PCT申请日1993年7月1日PCT公开专利PCT公开号WO94 / 01412。 1994年1月20日,公开了具有下式的孕激素激动剂:其中:A是 W不存在或-CH = CH-; R 1独立地选自卤素,-CF 3和NO 2,或者两个R 1可以连接形成-CH = CHCH = CH-的双基。 R 3独立地选自氢,C 1-6支链或直链烷基,卤素和-CF 3,条件是3-位的R 3必须为H,而4-位的R 3为H,或两个R 3可以连接形成选自-CH = CHCH = CH-,-C(NC1-4烷基2)= CHCH = CH-和-(CH2)4-的双基; R5选自H和Me;条件是R1和R3中只有一个形成稠合的双基;和立体异构体。

著录项

  • 公开/公告号EP0650480B1

    专利类型

  • 公开/公告日2001-11-21

    原文格式PDF

  • 申请/专利权人 ORTHO PHARMACEUTICAL CORPORATION;

    申请/专利号EP19930917006

  • 发明设计人 COMBS DONALD W.;

    申请日1993-07-01

  • 分类号C07D237/04;C07D409/04;C07F9/6509;A61K31/50;

  • 国家 EP

  • 入库时间 2022-08-22 00:37:34

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