Synthesis of Methyl 3-Azidothieno[2,3-b]pyridine-2-carboxylates and Application of the Huisgen Reaction

被引：8

作者：

Chaouni, Wafaa ^{[1
,2
]}

Aadil, Mina ^{[2
]}

Djellal, Ahmed ^{[1
]}

Kirsch, Gilbert ^{[1
]}

机构：

[1] Univ Lorraine, Inst Jean Barriol, UMR 7565, SRMSC,LIMBP, F-57070 Metz, France

[2] FST Mohammedia, LCBA, Mohammadia 20800, Morocco

来源：

ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES | 2014年 / 69卷 / 05期

关键词：

Vilsmeier-Haack-Arnold Reaction; 2-Chloro-3-cyano-pyridines; Thienopyridines; 1,2,3-Triazole; HERPESVIRUS POLYMERASES; BIOLOGICAL EVALUATION; DERIVATIVES; INHIBITORS; PYRIDOTHIENOPYRIMIDINES; PYRIDOTHIENOTRIAZINES; PYRIDINES; DESIGN; AGENTS;

D O I：

10.5560/ZNB.2014-3320

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The preparation of new substituted methyl 3-azidothieno[2,3-b]pyridine carboxylates by azotization of methyl 3-aminothieno[2,3-b]pyridine and subsequent treatment with sodium azide is described. Via Huisgen's 1,3-dipolar cycloaddition between substituted alkynes and the prepared azides, methyl 1,2,3-triazolo-thieno[2,3-b]pyridine carboxylates have been obtained.

引用

页码：509 / 518

页数：10

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