Procedure for obtaining a cephalosporin Compound of formula (i), or salts thereof, wherein R1 is a nitrogen-containing Heterocyclic radical - Uncle; R2 is Hydrogen, Hydroxy, and R3, R4 and R5 is Hydrogen, Hydroxy, or aciloxi.Based on the condensation reaction of a compound of formula (i) or its Salt, a compound of formula (iii), in which R1, R2, R3, R4 and R5 have the meanings indicated above. The reaction is carried out in an Inert Organic Solvent, in the presence or absence of a basic sililacion Reagent and at a temperature between 50 - 50 GC and GC.These compounds have pharmacological applications for its antibacterial activity. * * formula
展开▼
机译:获得式(i)的头孢菌素化合物或其盐的方法,其中R 1为含氮杂环基-叔叔; R 2为氢,羟基,R 3,R 4和R 5为氢,羟基或阿昔洛西。基于式(i)的化合物或其盐的缩合反应,式(iii)的化合物,其中R 1,R 2 R 3,R 4和R 5具有以上所示的含义。反应是在惰性有机溶剂中,在有或没有碱性硅化试剂的条件下,在50至50 GC和GC之间的温度下进行的。这些化合物因其抗菌活性而具有药理学应用。 * *公式
展开▼