HRID552511

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID693283

4-bromopyridine-2-carbonitrile

C6H3BrN2

结构：Cc1cc(B2OC(C)(C)C(C)(C)O2)cc(C(=O)Nc2ccnc(Cl)c2)n1

HCID49760409

N-(2-Chloropyridin-4-yl)-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxamide

C18H21BClN3O3

PRODUCTS

生成物

结构：Cc1cc(-c2ccnc(C#N)c2)cc(C(=O)Nc2ccnc(Cl)c2)n1

HCID86614584

未命名化合物

PROCEDURE

实验过程

The title compound, was prepared from 6-Methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine-2-carboxylic acid (2-chloro-pyridin-4-yl)-amide in accordance with the general method of example 131, step 2 using 4-Bromo-2-cyanopyridine instead of 3-Trifluoromethyl-5-bromopyridine to yield the final compound as a white solid, MS (ISP): m/e=350.2, 352.2 (M+H)+.