HRID216944

反应详情

EQUATION

反应方程式

HRID 216944 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
85 °C

PROCEDURE

实验过程

(S)-tert-Butyl 4-(1-amino-1-oxo-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 16, step (i), 200 mg) and 5-bromo-2-methylbenzonitrile (80 mg) in acetonitrile (8 mL) were treated with an aqueous solution of sodium carbonate (2M, 0.387 mL) and nitrogen was bubbled through the mixture. 1,1 bis(Di-tert-butylphosphino)ferrocene palladium dichloride (5 mg) was added and the mixture was heated at 85° C. for 18 h. The mixture was concentrated and purified by chromatography on silica eluting with 50 to 100% ethyl acetate/isohexane to afford the sub-titled compound (154 mg).

WORKUP

后处理

  1. customwas bubbled through the mixture
  2. addition1,1 bis(Di-tert-butylphosphino)ferrocene palladium dichloride (5 mg) was added
  3. concentrationThe mixture was concentrated
  4. custompurified by chromatography on silica eluting with 50 to 100% ethyl acetate/isohexane