HRID1261359

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CSc1cc2nccc(Oc3ccc([N+](=O)[O-])cc3F)c2s1

HCID59424488

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

C14H9FN2O3S2

结构：CC(C)(C)[Si](C)(C)OC1CN(C(=O)c2cc3nccc(Cl)c3s2)C1

HCID59424656

未命名化合物

PRODUCTS

生成物

结构：O=C(c1cc2nccc(Oc3ccc([N+](=O)[O-])cc3F)c2s1)N1CC(O)C1

HCID59424556

未命名化合物

收率 39%

PROCEDURE

实验过程

Starting from the amide 297 and following the procedure described above for the synthesis of compound 230 (scheme 50, example 203), title compound 298 was obtained in 39% yield as a syrup. MS (m/z): 389.05 (M+1).