首页> 外国专利> PROCESS FOR PREPARATION OF 1-ETHYL-4- {3-3-ETHYL- 6, 7-DIHYDRO-7- OXO-2- (PYRIDYLMETHYL) -2H- PYRAZOLO 4, 3-d PYRIMIDIN- 5-YL -4- PROPOXYSULFONYL}- PIPERAZINE AND THE 4-2-SUBSTITUTED-5-(4-ETHYL- 1-PIPERAZINYLSULPHONYL)- BENZAMIDO-5-ETHYL-1- (2-PYRIDYLMETHYL) 1H-PYRAZOLE-3-CARBOXAMIDE INTERMEDIATES THEREFOR

PROCESS FOR PREPARATION OF 1-ETHYL-4- {3-3-ETHYL- 6, 7-DIHYDRO-7- OXO-2- (PYRIDYLMETHYL) -2H- PYRAZOLO 4, 3-d PYRIMIDIN- 5-YL -4- PROPOXYSULFONYL}- PIPERAZINE AND THE 4-2-SUBSTITUTED-5-(4-ETHYL- 1-PIPERAZINYLSULPHONYL)- BENZAMIDO-5-ETHYL-1- (2-PYRIDYLMETHYL) 1H-PYRAZOLE-3-CARBOXAMIDE INTERMEDIATES THEREFOR

机译:制备1-乙基-4- {3- [3-乙基-3-6,7-二羟基-7-氧代-2-(吡咯甲基))-2H-吡唑并[4,3-d]吡唑啉-5-基的方法-4-丙氧磺酰基}-哌嗪和4- [2-取代的5-(4-乙基-1-1-吡嗪基磺酰基)-苯甲酰氨基] -5-乙基-1-(2-吡啶二甲基)1H-吡唑-3-羧酰胺中间体那个

摘要

A process for the preparation of a compound of the formula 3761 כ" ז בשבט התשס" ד - February 19, 2004 comprising reacting a compound of the formula in the presence of -OR, wherein R is CH2 CH2CH3, where X is selected from the group consisting of arylsulphonyloxy, C4 alkylsulphonyloxy, nitro or halo substituted benzenesulphonyloxy, C1-C4 perfluoroalkylsulphonyloxy, optionally substituted aroyloxy, C1-C4 perfluoroalkanoyloxy, C1-C4 alkanoyloxy, halo, diazonium, methoxy, oxonium, perchloryloxy, quaternaryammonium C1-C4 alkylsulphonyloxy, halosulphonyloxy, halonium and diarysulphonylamino. Compounds of formula IIB are claimed as new.
机译:制备式3761的化合物的方法-2004年2月19日,包括在-OR的存在下使式的化合物反应,其中R为CH2 CH2CH3,其中X选自芳基磺酰氧基,C 4烷基磺酰氧基,硝基或卤素取代的苯磺酰氧基,C 1 -C 4全氟烷基磺酰氧基,任选取代的芳酰氧基,C 1 -C 4全氟烷酰氧基,C 1 -C 4烷酰氧基,卤代,重氮基,甲氧基,氧鎓,过氯酰氧基,仲氯氧基,ha和二磺酰基氨基。要求保护式IIB化合物是新的。

著录项

  • 公开/公告号IL152926B

    专利类型

  • 公开/公告日2004-02-19

    原文格式PDF

  • 申请/专利权人 PFIZER IRELAND PHARMACEUTICALS;

    申请/专利号IL152926

  • 发明设计人

    申请日2002-11-18

  • 分类号7C07DA;

  • 国家 IL

  • 入库时间 2022-08-21 23:10:35

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