HRID1821250

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：Cc1ccc(S(=O)(=O)n2ccc3c(B4OC(C)(C)C(C)(C)O4)ccnc32)cc1

HCID49758926

1-(4-Methylbenzene-1-sulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine

C20H23BN2O4S

结构：Cc1nc(-c2ccc([N+](=O)[O-])cc2)c(Br)s1

HCID68998100

5-Bromo-2-methyl-4-(4-nitrophenyl)thiazole

C10H7BrN2O2S

PRODUCTS

生成物

结构：Cc1ccc(S(=O)(=O)n2ccc3c(-c4sc(C)nc4-c4ccc([N+](=O)[O-])cc4)ccnc32)cc1

HCID69001198

未命名化合物

PROCEDURE

实验过程

Following the procedure described for Intermediate 6 with 5-bromo-2-methyl-4-(4-nitrophenyl)-1,3-thiazole and [(4-methylphenyl)sulfonyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine provided title compound. ESMS [M+H]+: 491.2