节点文献
硫酸头孢喹肟的合成
Synthesis of Cefquinome Sulfate
【摘要】 头孢噻肟用六甲基二硅胺烷保护氨基和羧基后与三甲基碘硅烷进行取代反应,与5,6,7,8-四氢喹啉进行3-位取代后用甲醇处理得到头孢喹肟氢碘酸盐,阴离子交换树脂除去碘离子后与硫酸成盐,得抗生素硫酸头孢喹肟一水合物,总收率约48%。
【Abstract】 The amido group and carboxyl group of cefotaxime were protected by reacting with hexamethyl disilazane, then underwent 3-substistution by trimethyliodosilane and 5,6,7,8-tetrahydroquinoline successively, and treated with methanol to obtain cefquinome hydroiodide, which after ion exchange to remove the iodide and neutralized with sulfuric acid to give cefquinome sulfate in 48% overall yield.
- 【文献出处】 中国医药工业杂志 ,Chinese Journal of Pharmaceuticals , 编辑部邮箱 ,2007年06期
- 【分类号】R914
- 【被引频次】14
- 【下载频次】494