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Reaction of 2-aminobenzimidazole with bifunetional carboxylie acid derivatives. Formation of pyrimido[1,2-a] benzimidazolones†
Journal of Heterocyclic Chemistry ( IF 2.0 ) Pub Date : February 1973 , DOI: 10.1002/jhet.5570100116
A. W. Chow , D. R. Jakas , B. P. Trotter , N. M. Hall , J. R. E. Hoover

2-Aminobenzimidazole reacts with α,β-unsaturated carboxylic acid chlorides or esters to give only pyrimido [1,2-a] benzimidazol-2-(1H) ones. β-Ethoxymethylenemalonie acid derivatives or β-ketocarboxylic acid derivatives give only pyrimido [1,2-a] benzimidazol-4-(1H)ones. Structural assignments based on nmr and chemical manipulations are discussed.

中文翻译:

2-氨基苯并咪唑与双官能羧酸衍生物的反应。嘧啶基[1,2-a]苯并咪唑酮的形成

2-氨基苯并咪唑与α,β-不饱和羧酸氯化物或酯反应,仅得到嘧啶基[1,2 - a ]苯并咪唑-2-(1 H)。β-乙氧基亚甲基丙二酸衍生物或β-酮羧酸衍生物仅给出嘧啶基[1,2 - a ]苯并咪唑-4-(1 H)酮。讨论了基于核磁共振和化学操作的结构分配。
更新日期:2017-01-31
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