Regioselective synthesis of 7,8-dihydroimidazo [5,1-c][1,2,4]triazine-3,6(2H,4H)-dione derivatives: A new drug-like heterocyclic scaffold

被引:12
|
作者
Tzvetkov, Nikolay T. [1 ]
Euler, Harald [2 ]
Mueller, Christa E. [1 ]
机构
[1] Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, Pharmaceut Sci Bonn PSB, D-53121 Bonn, Germany
[2] Univ Bonn, Steinmann Inst Mineral, D-53115 Bonn, Germany
关键词
hydantoins; hydrazides; imidazotriazines; N-alkylation; regio- and chemoselective reaction; thionation; X-ray structure; STRUCTURE ELUCIDATION; IDENTIFICATION; LIPOPHILICITY; ANTITUMOR; ESTERS; RING;
D O I
10.3762/bjoc.8.181
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Dihydroimidazo[5,1-c][1,2,4]triazine-3,6(2H, 4H)-dione derivatives were prepared by successive N3- and N1-alkylation of hydantoins, followed by regioselective thionation and subsequent cyclization under mild conditions. In a final alkylation step a further substituent may be introduced. The synthetic strategy allows broad structural variation of this new drug-like heterobicyclic scaffold. In addition to extensive NMR and MS analyses, the structure of one derivative was confirmed by X-ray crystallography.
引用
收藏
页码:1584 / 1593
页数:10
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