HRID1261263

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11275251

7-Chlorothieno[3,2-b]pyridine

C7H4ClNS

结构：CN(C)C(=O)c1cc2nccc(Oc3ccc([N+](=O)[O-])cc3F)c2s1

HCID59424475

未命名化合物

PRODUCTS

生成物

结构：O=[N+]([O-])c1ccc(Oc2ccnc3ccsc23)c(F)c1

HCID59424682

7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridine

C13H7FN2O3S

收率 45%

PROCEDURE

实验过程

Starting from the chloride 2 (scheme 1) and following the procedure described above for the synthesis of compound 6 (scheme 1, example 1), title compound 168 was obtained in 45% yield. LRMS (M+1) 290.3 (100%).