首页> 外国专利> Process for the formation of a group of mono primary phosphorylates a functionality of 1,2 - diol - propanu00f3ila terminal, processes for the preparation of 5 - (HET - X - methyl) - 3 - (4 - (1 - benzyl - 1,2,5,6 - tetraidropirid - 4 - YL) - 3.5 - difluorofenil) oxazolidin - 2 - ona, and 5 - isoxazol - 3 - iloximetil - 3 - (4 - (1 - benzyl - 1,2,5,6 - tetraidrop Irid - 4 - YL) - 3.5 - difluorofenil) oxazolidin - 2 - ona, and.Intermediate compound quu00ecmico

Process for the formation of a group of mono primary phosphorylates a functionality of 1,2 - diol - propanu00f3ila terminal, processes for the preparation of 5 - (HET - X - methyl) - 3 - (4 - (1 - benzyl - 1,2,5,6 - tetraidropirid - 4 - YL) - 3.5 - difluorofenil) oxazolidin - 2 - ona, and 5 - isoxazol - 3 - iloximetil - 3 - (4 - (1 - benzyl - 1,2,5,6 - tetraidrop Irid - 4 - YL) - 3.5 - difluorofenil) oxazolidin - 2 - ona, and.Intermediate compound quu00ecmico

机译:形成一组单伯磷酸化基团的功能为1,2-二醇-丙烷末端的方法,制备5-(HET-X-甲基)-3-(4-(1-苄基- 1,2,5,6-四氟哌啶-4-YL)-3.5-二氟苯腈)恶唑烷定-2-ona和5-异恶唑-3-iloximetil-3-(4-(1-苄基-1,2,5, 6-四滴子Irid-4-YL)-3.5-二氟苯腈)恶唑烷丁酯-2-ona和中间体化合物Qu u00ecmico

摘要

Process for the formation of a group of monofosforila primary functionality of 1,2 - diolpropanou00ecla terminal, processes for the preparation of 5 - (HET - X - methyl) - 3 - (4 - (1 - benzyl - 1,2,5,6 - tetraidropirid - 4il) - 3, 5 - difluorofenil) oxazolidin - 2 - ona, and 5 - isoxazol3 - iloximetil - 3 - (4 - (1 - benzyl - 1,2,5,6 - tetraidropi rid - 4 - YL) - 3,5difluorofenil) oxazolidin - 2 - ona, and.Intermediate compound quu00ecmico ".The invention relates to chemical processes and chemical intermediates which are useful in the formation of a selective group of mono phosphorylates primary (- OPO (oh ~ 2 ~)) in a system containing 1.2 - diol - propanou00edla (Hoch ~ 2 ~ ch (OH) - co) terminal.The chemical processes and chemical intermediates and processes for their manufacture) are particularly useful for the manufacture of oxazolidinone agents anti gram positive bacterial containing such Fu.Ncionalidade, particularly for the preparation of 5 (R) isoxazol - 3 - iloximetil - 3 - (4 - (1 - (2 (s) - hydroxy - 3 - fosforil - propanoil) - 1,2,5, 6 - tetraidropiridi - 4-yl) 3,5 - difluorofenil) oxazolidin - 2 - one.
机译:形成一组单氟磺酰基初级官能团的1,2-二醇丙醇末端的方法,制备5-(HET-X-甲基)-3-(4-(1-苄基-1,2, 5,6-四氟哌啶-4il)-3,5-二氟苯腈)恶唑烷-2-ona和5-异恶唑3-iloximetil-3-(4-(1-苄基-1,2,5,6-四氟哌啶-4 -YL)-3,5-二氟苯腈)恶唑烷-2.-中间体,以及中间体化合物。本发明涉及用于形成选择性的单磷酸酯基伯(-OPO)的选择性基团的化学方法和化学中间体。 (oh〜2〜))在包含1.2-二醇-丙醇(Hoch〜2〜ch(OH)-co)末端的系统中。化学过程和化学中间体及其制造方法)对于制造特别有用恶唑烷酮类抗革兰氏阳性细菌的药物,其中含有此类Fu.Ncionalidade,特别是用于制备5(R)的异恶唑-3-iloximetil- 3-(4-(1-(2(s)-羟基-3-fosforil-丙烷油)-1,2,5,6-四氟哌啶-4-基)3,5--二氟苯腈)恶唑烷-2-一。

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