首页> 外国专利> Method for Preparation of fluoro naftalen - 8 - 1 - ilamina and use this to obtain a favorable Synthesis of 7 - (4 - 4 - (5 - fluoro - naftalen - 1 - il) piperazin-1-yl - Butoxy} - 3, 4 - dihydro 1H - 1, 8 naftiridin - 2 - ona

Method for Preparation of fluoro naftalen - 8 - 1 - ilamina and use this to obtain a favorable Synthesis of 7 - (4 - 4 - (5 - fluoro - naftalen - 1 - il) piperazin-1-yl - Butoxy} - 3, 4 - dihydro 1H - 1, 8 naftiridin - 2 - ona

机译:制备氟代萘芬-1-基-1-萘胺的方法,并用该方法得到有利的7-(4- [4-(5--氟代萘芬-1-基)哌嗪-1-基]-丁氧基}的合成。 3,4-二氢1H-[1,8] naftiridin-2-ona

摘要

Describes a procedure for the preparation of fluoro naftalen - 8 - 1 - ilamina comprising reacting 1H - Naphtho [1,8] - [1,2,3] triazine with Hydrogen fluoride or a complex of hydrogen fluoride and a base n donor.It also suggests a procedure to use 8 - fluoro naftalen - 1 - ilamina produced as described above for the preparation of 1 - (5 - fluoro - naftalen - 1 - il) - piperazine can be used as an intermediate in the production of 7 - (4 - [4 - (8 - fluoro naftalen - 1 - IL) - piperazin.Il - 1} - butoxy] - 3,4-dihydro - 1H - [1,8] naftiridin - 2 - ona, a partial D2 agonist indicated for possible use in the treatment of schizophrenia.
机译:描述了一种制备氟代萘芬特(naftalen)-8-1-Ilamina的方法,该方法包括使1H-Naphtho [1,8]-[1,2,3]三嗪与氟化氢或氟化氢与碱n供体的配合物反应。还建议了使用如上所述制备的8-氟代萘芬特-1-丙胺用于制备1-(5-氟代-萘芬特-1-1-1)-哌嗪可用作生产7-(- 4-[4-(8-氟代萘芬-1-IL)-哌嗪.II-1}-丁氧基]-3,4-二氢-1H-[1,8]萘替丁-2-ona,表示部分D2激动剂。用于治疗精神分裂症。

著录项

  • 公开/公告号AR056154A1

    专利类型

  • 公开/公告日2007-09-19

    原文格式PDF

  • 申请/专利权人 PFIZER PRODUCTS INC.;

    申请/专利号AR2006P104638

  • 发明设计人

    申请日2006-10-24

  • 分类号C07C211/59;C07D253/08;C07D295/073;

  • 国家 AR

  • 入库时间 2022-08-21 20:59:34

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