An efficient, large-scale synthesis of cytenamide

被引:2
|
作者
Bedford, Colin T. [1 ]
机构
[1] UCL, Christopher Ingold Lab, Dept Chem, London WC1H 0AJ, England
关键词
cytenamide; dibenzosuberenone; 5H-dibenzo[a; d; cyclohepten-5-one; 5H-5-chlorodibenzo[a; cycloheptene; 5H-5-cyanodibenzo[a; d]cycloheptene; d]cyclo heptene-5-carboxamide; ACID SOLVATE; INHIBITORS;
D O I
10.3184/174751918X15218087557053
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dibenzosuberenone (5H-dibenzo[a,d] cyclohepten-5-one) was reduced to the corresponding alcohol by sodium borohydride/MeOH and converted to the corresponding 5-chloro compound by thionyl chloride/benzene, treatment of which with CuCN/toluene gave the corresponding nitrile. Hydrolysis by ethanolic KOH yielded the corresponding amide, cytenamide (5H-dibenzo[a,d]cycloheptene-5carboxamide).
引用
收藏
页码:153 / 155
页数:3
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