HRID1989556
反应详情
EQUATION
反应方程式
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反应物
PRODUCTS
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PROCEDURE
实验过程
The title compound was prepared from 2-(3-bromo-phenyl)-4-(3,4-dichloro-phenyl)-6-methyl-pyridine (example E.85) (0.20 g, 0.509 mmol) and commercially available 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (0.123 g, 0.56 mmol) according to the general procedure VI. Obtained as an off-white solid (0.050 g, 21%). MS (ISP) 406.0 [(M+H)+], 408.1 [(M+2+H)+] and 410 [(M+4+H)+]; mp 99° C. (dec.).