HRID1512138

反应详情

EQUATION

反应方程式

HRID 1512138 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
120 °C

PROCEDURE

实验过程

To an argon flushed mixture of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine (42 mg, 0.19 mmol), 6-chloro-N-methyl-2-morpholino-N-(tetrahydro-2H-pyran-4-yl)pyrimidin-4-amine (12 mg, 0.038 mmol) in THF (0.8 mL), and aq. Na2CO3 (2M, 0.27 mL) in a pressure vessel, was added dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloromethane adduct (8 mg, 0.0095 mmol) in one portion. The pressure vessel was sealed and the mixture was heated in a microwave at 120° C. for 600 seconds. The crude mixture was filtered, concentrated under reduced pressure and purified by reverse phase preparative HPLC to give N6-methyl-2-morpholino-N6-(tetrahydro-2H-pyran-4-yl)-4,5′-bipyrimidine-2′,6-diamine (4.6 mg, 32%). LC/MS (m/z): 372.2 (MH+), Rt 1.76 minutes.

WORKUP

后处理

  1. customTo an argon flushed
  2. customThe pressure vessel was sealed
  3. filtrationThe crude mixture was filtered
  4. concentrationconcentrated under reduced pressure
  5. custompurified by reverse phase preparative HPLC