摘要
以氯乙酰氯为原料,经6步反应合成目标化合物,总收率27.7%。目标产物的光谱数据与文献报道一致。该工艺原料和试剂价廉易得,条件温和,反应总收率高,更适合工业化生产。
The target compound was synthesized via 6 steps from chloroacetyl chloride in 27.7% overall yield. Its spectral data were identical with those reported in literature. A more practical, effciently, economic process for synthesis of disodium ticarcillin is worked out.
出处
《中国药物化学杂志》
CAS
CSCD
2006年第3期178-179,共2页
Chinese Journal of Medicinal Chemistry
关键词
药物化学
工艺改进
化学合成
替卡西林钠
抗生素
medicinal chemistry
process improvement
chemical synthesis
disodium ticarcillin
antibiotics