HRID511335

反应详情

EQUATION

反应方程式

HRID 511335 的结构方程式

PROCEDURE

实验过程

The title compound was prepared using the procedure from Example 97 with Diethyl (4-{[4-{[4-bromo-2-(methylcarbamoyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-2-yl]amino}benzyl)phosphonate (Example 106) and 1-[4-(tert-butyl-dimethyl-silanyloxy)-cyclohexyl]-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (Compound 137A). After Suzuki reaction and SPE pre-purification, dried material was dissolved in DCM and 1.0 M HCl in ether was added. The mixture was stirred at room temperature for half an hour. The crude was sent to MDP for purification. MS (ES+): m/z 702.34 (100) [MH+]; HPLC: tR=0.96 min (UPLC, purity).

WORKUP

后处理

  1. customAfter Suzuki reaction
  2. custompre-purification, dried material
  3. dissolutionwas dissolved in DCM
  4. addition1.0 M HCl in ether was added
  5. customThe crude was sent to MDP for purification