首页> 外国专利> METHOD OF OBTAINING NOVEL DERIVATIVES OF PYRIDINE, METHOD OF OBTAINING HYDROXY-SUBSTITUTED DERIVATIVES OF PYRIDINE, METHOD OF OBTAINING DERIVATIVES OF OXIRANYLPYRIDINE, NOVEL DERIVATIVES OF 3-(1,2=DIHYDROXYETHYL)PYRIDINE, NOVEL DERIVATIVES OF 2-PYRIDIN-3-YL-2-HYDROXYETHYLENIC ESTER, NOVEL DERIVATIVES OF PYRIDINE, NOVEL DERIVATIVES OF (DI)OXYDIOXATHIOLANYLPYRIDINE, NOVEL DERIVATIVES OF T-BUTYL2R-4-AMINOFHENYL)ETHYL-2-HYDROXY-2-PYRIDIN-3-YLETHYLCARBAMINIC ESTER, NOVEL DERIVATIVES OF T-BUTYL2R-4-AMINOPHENYL)ETHYL-2-(TERT-BUTYLODIMETHYLSILANYLOXY)-2-PYRIDIN-3-YLETHYLCARBAMINIC ESTER, 2R-4-AMINOPYHENYL)ETHYL-2-(TERT-BUTYLODIMETHYLSILANYLOXY)-2-(6-CHLOROPYRIDIN-3-YL)ETHYL--2-(NITROPHENYL)ETHYLCARBAMINIC ESTER AND NOVEL DERIVATIVES OF 3-{1-TERT-BUTYLODIMETHYLSILANYLOXY)-2-2--(NITROPHENYL)ETHYLAMINOETHYL}PYRIDINE

METHOD OF OBTAINING NOVEL DERIVATIVES OF PYRIDINE, METHOD OF OBTAINING HYDROXY-SUBSTITUTED DERIVATIVES OF PYRIDINE, METHOD OF OBTAINING DERIVATIVES OF OXIRANYLPYRIDINE, NOVEL DERIVATIVES OF 3-(1,2=DIHYDROXYETHYL)PYRIDINE, NOVEL DERIVATIVES OF 2-PYRIDIN-3-YL-2-HYDROXYETHYLENIC ESTER, NOVEL DERIVATIVES OF PYRIDINE, NOVEL DERIVATIVES OF (DI)OXYDIOXATHIOLANYLPYRIDINE, NOVEL DERIVATIVES OF T-BUTYL2R-4-AMINOFHENYL)ETHYL-2-HYDROXY-2-PYRIDIN-3-YLETHYLCARBAMINIC ESTER, NOVEL DERIVATIVES OF T-BUTYL2R-4-AMINOPHENYL)ETHYL-2-(TERT-BUTYLODIMETHYLSILANYLOXY)-2-PYRIDIN-3-YLETHYLCARBAMINIC ESTER, 2R-4-AMINOPYHENYL)ETHYL-2-(TERT-BUTYLODIMETHYLSILANYLOXY)-2-(6-CHLOROPYRIDIN-3-YL)ETHYL--2-(NITROPHENYL)ETHYLCARBAMINIC ESTER AND NOVEL DERIVATIVES OF 3-{1-TERT-BUTYLODIMETHYLSILANYLOXY)-2-2--(NITROPHENYL)ETHYLAMINOETHYL}PYRIDINE

机译:获得吡啶的新衍生物的方法,获得吡啶的羟基取代的衍生物的方法,获得氧吡喃吡啶的衍生物的方法,3-(1,2 =二吡啶基-乙烯基吡啶基)吡啶的新颖衍生物2-羟基乙氧基酯,吡啶的新颖衍生物,(二)羟基二氧代邻苯二甲酰基吡啶的新颖衍生物,叔丁基[2R-4-亚氨基苯基]乙基]-[2-羟基-2-吡啶基-3-乙基酯的新颖衍生物叔丁基[2R-4-氨基苯甲基]-[2-(叔丁基二甲基硅基己氧基)-2-吡啶基-3-乙基]氨基酯,[2R-4-氨基苯基]乙基]-[2-(叔丁二甲基二硅氧烷)-2-(6-氯吡啶-3-基)乙基]-[-2-(硝基苯基)乙基]碳酰胺和3- {1-叔丁二甲基硅烷基)-2-衍生物[[2- -((硝基苯基)乙基]氨基]乙基}吡啶

摘要

A process for preparing a compound of the formula CHEM wherein n, R1, R2, R3 and X are as defined above, used as an intermediate in the synthesis of beta -adrenergic receptor agonists.
机译:制备式化合物的方法,其中n,R 1,R 2,R 3和X如上定义,用作合成β-肾上腺素能受体激动剂的中间体。

著录项

  • 公开/公告号PL346805A1

    专利类型

  • 公开/公告日2001-10-08

    原文格式PDF

  • 申请/专利权人 PFIZER PRODUCTS INC.;

    申请/专利号PL20010346805

  • 发明设计人 DOW ROBERT LEE;SCHNEIDER STEVEN ROY;

    申请日2001-03-30

  • 分类号C07F7/10;

  • 国家 PL

  • 入库时间 2022-08-22 01:24:03

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