HRID500841

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11173165

未命名化合物

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=C(c1cc2nccc(Oc3ccc([N+](=O)[O-])cc3F)c2s1)N1CCCC1

HCID59424552

[7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl]-1-pyrrolidinylmethanone

C18H14FN3O4S

收率 93%

PROCEDURE

实验过程

Starting from (7-chlorothieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanone (139, scheme 26) and following the procedure described above for the synthesis of compound 6 (scheme 1, example 1), title compound 193 was obtained in (93% yield). LRMS (M+1) 387.4 (100%).