HRID39051

反应详情

EQUATION

反应方程式

HRID 39051 的结构方程式

PROCEDURE

实验过程

A mixture of intermediate 1-5 (4.02 g, 12 mmol), 2-(2,4-dimethyl-thiazol-5-yl)-quinoline-6-boronic acid 16-1 (4.58 g, 1.19 eq, synthesized as described in WO2006/076529), K2CO3 (5.13 g, 3.1 eq) and dichloro-bis(triphenylphosphino)-Pd(II) (0.86 g, 0.10 eq) in ethanol/toluene (1:1, 80 mL) was stirred at room temperature under N2 overnight. After concentration under reduced pressure, the reaction mixture was redissolved in ethyl acetate and washed with a 5 M NaHCO3 solution. The obtained yellow precipitate was filtered off, washed with water, then isopropanol to give 4.13 g (67%) of 3-Cyclohexyl-2-[2-(2,4-dimethyl-thiazol-5-yl)-quinolin-6-yl]-1H-indole-6-carboxylic acid methyl ester 16-2 as a yellow solid; m/z=496 (M+H+).

WORKUP

后处理

  1. concentrationAfter concentration under reduced pressure
  2. dissolutionthe reaction mixture was redissolved in ethyl acetate
  3. washwashed with a 5 M NaHCO3 solution
  4. filtrationThe obtained yellow precipitate was filtered off
  5. washwashed with water