反应条件
1: 3-hydroxy-1,3-dihydro-7-chloro-5-phenyl-2H-1,4-benzodiazepin-2-one With sodium hydride in tetrahydrofuran
T=20°C; deprotonation; 0.5 h;
2: succinic acid anhydride in tetrahydrofuran
T=40°C; Addition; esterification; 2 h;
参考文献
Janssen; Hulst; Kellogg; Hendriks; Ensing; De Zeeuw
Pharmazie, 2000 , vol. 55, # 1 p. 42 - 48