摘要
以δ 戊内酯和环己胺为原料合成了抗血小板聚集药物西洛他唑的重要中间体N 环己基 5 氯丁基 1H 四氮唑 。
N cyclohexyl 5 (4' chlorobutyl) 1H tetrazole was synthesized by a convenient process from δ valerolactone and cyclohexylamine. Appropriate cyclocondensation reagent and phase transfer catalyst were selected. The yield of product is 78%. The product is an important intermediate for producing drugs of blood platelets aggregation inhibitors.
出处
《合成化学》
CAS
CSCD
2003年第2期150-152,共3页
Chinese Journal of Synthetic Chemistry