首页> 外国专利> Derivatives of 1,3 dihydro - 1 - (fenilalquenil) - 2H - imidazol - 2 - One, Process for their preparation, compositions containing Same,Procedure for and elicit that Composition and use of such compounds for preparing medicaments.

Derivatives of 1,3 dihydro - 1 - (fenilalquenil) - 2H - imidazol - 2 - One, Process for their preparation, compositions containing Same,Procedure for and elicit that Composition and use of such compounds for preparing medicaments.

机译:1,3-二氢-1-(苯甲腈)-2H-咪唑-2-的衍生物,其制备方法,含有该衍生物的组合物,该化合物的制备方法和用途以及此类化​​合物在制备药物中的用途。

摘要

1. The invention refers to derivatives of 1,3-dihydro-1 (derivatives of phenyl-2h-pyridan-2-ona formula (I)), positive oxidation form, salt water added with acceptable acid or drug base on medicine and chemically acceptable plasma form. In these derivatives, R1 and R2 are hydrogen, C1-6 tar respectively, Formaldehyde, trifluoromethyl, cyclopropylpropylpropyl, a saturated 5 -,6- or 7 members containing one or two heteroatoms selected from oxygen, sulfur or nitrogen, indanyl, bicyl (2.2.1) -2-heptenyl, bicyl (2.2.1) heptanyl, C1-6 alkylsulfonyl, arylsulfonyl or substituted C1-10 alkyl ; R3 is hydrogen, halo or C1-6 alkynyloxy; R4 is hydrogen, cyano, optionally substituted C1-6 alkyl, C1-6 alkyloxycarbonyl or aryl; R5 is hydrogen, cyano; optionally substituted C1-6 alkyl, C1-6 alkyloxycarbonyl or aryl. Y is a direct bond or C1-3 alkanediyl; -A-B- is a bivalent radical having the formula -CR6 = CR7- or -CHR6-CHR7-. L is hydrogen, optionally substituted C1-6 alkyl C1-6 alkylcarbonyl, C1-6 alkyloxycarbonyl,C1-6 or arilsulfonil tar; arilo is the substituted phenyl. The definition of ldebe is supplemented by the following alternatives: alquenilo C3-6, arilo, pirideni, C1-C4 oarialoal quilo C1-C4. Het is mofflin or alternative pyridine glycol, pyridine, pyridine, furan or smallpox. Definition of alternative isoprene, furan, pyridine or tienilo with chlordecone and PDE IV inhibitor activity.1. Preparation procedure and use of compounds and compounds
机译:1.本发明涉及1,3-二氢-1(苯基-2h-吡啶-2-ona式(I)的衍生物),正氧化形式,加有可接受的酸或药物的盐水,基于药物和化学方法可接受的血浆形式。在这些衍生物中,R1和R2分别为氢,C1-6焦油,甲醛,三氟甲基,环丙基丙基丙基,含有一个或两个选自氧,硫或氮的杂原子的饱和5-,6-或7元,茚满基,二苄基(2.2 .1)-2-庚烯基,bicyl(2.2.1)庚基,C1-6烷基磺酰基,芳基磺酰基或取代的C1-10烷基; R 3是氢,卤素或C 1-6炔氧基; R4是氢,氰基,任选取代的C1-6烷基,C1-6烷氧羰基或芳基; R5是氢,氰基;任选取代的C 1-6烷基,C 1-6烷氧基羰基或芳基。 Y是直接键或C 1-3烷二基; -A-B-是具有式-CR6 = CR7-或-CHR6-CHR7-的二价基团。 L为氢,任选取代的C 1-6烷基,C 1-6烷基羰基,C 1-6烷氧基羰基,C 1-6或阿立磺腈焦油;芳基是取代的苯基。 ldebe的定义由以下替代方法补充:alquenilo C3-6,arilo,pirideni,C1-C4唾液基quilo C1-C4。 Het是mofflin或替代的吡啶二醇,吡啶,吡啶,呋喃或天花。定义具有十氯酮和PDE IV抑制剂活性的异戊二烯,呋喃,吡啶或替尼洛1。化合物的制备方法和用途

著录项

  • 公开/公告号AR003412A1

    专利类型

  • 公开/公告日1998-08-05

    原文格式PDF

  • 申请/专利权人 JANSSEN PHARMACEUTICA N.V.;

    申请/专利号AR20100207796

  • 发明设计人

    申请日1996-04-03

  • 分类号C07D233/32;A61K31/415;A61K31/4166;A61P11;A61P17;A61P29;A61P37/08;C07D233/38;C07D233/70;

  • 国家 AR

  • 入库时间 2022-08-22 02:58:47

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