📜(6R,7R)-7-[(Z)-2-(5-Amino-[1,2,4]Thiadiazol-3-yl)-2-Trityloxyiminoacetylamino]-8-Oxo-3-[(E)-(R)-2-Oxo-[1,3']Bipyrrolidinyl-3-Ylidenemethyl]-5-Thia-1-Azabicyclo[4.2.0]oct-2-Ene-2-Carboxylic Acid 以49的收率获得头孢吡普
参考文献:Derivatives Of 3-(2-Oxo-[1,3']Bipyrrolidinyl-3-Ylidenemethyl)-Cephams
标题:Derivatives Of 3-(2-Oxo-[1,3']Bipyrrolidinyl-3-Ylidenemethyl)-Cephams
摘要:本发明提供了式i的化合物,其中r1为氢,C1-6-烷基,C1-6-烷基取代氟,或c3-6-环烷基;R2为氢或从群组中选择的取代基,该群组包括-ch2C(═chr)-coor,-ch2ocor,-ch(R)ocor,-ch(R)ocoor,-ch(ocor)ocor,-ch2Coch2ocor和r3为氢或从群组中选择的取代基,该群组包括-ch2C(═ch2)-coor,-cooch2C(═chr)-coor,-cooch2ocor,-cooch(R)ocor,-cooch(R)ocoor,-cooch(ocor)ocor,-cooch2Coch2ocor,且其中r2和r3中的一个为氢,另一个不是氢,R为氢或c1-6-烷基;R4为氢或羟基,R5为氢或&ohgr;-羟基烷基;X为ch或n,这些化合物的药学上可接受的盐和它们的盐的水合物.