反应 #554624

ord-68d246155c0e4a528a24dd8480f2a2ec

反应方程式

Nc1ccnc(OCc2ccc(CNC(=O)C(F)(F)F)cc2)n1
N-(4-((4-Aminopyrimidin-2-yloxy)methyl)benzyl)-2,2,2-trifluoroacetamide
CN
methylamine
NCc1ccc(COc2nccc(N)n2)cc1
2-(4-(Aminomethyl)benzyloxy)4-aminopyrimidine

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他all volatiles are removed in vacuo
  2. 2
    其他The product is used without further purification in the next step

实验过程

150 mg (0.46 mmol) of N-(4-((4-Aminopyrimidin-2-yloxy)methyl)benzyl)-2,2,2-trifluoroacetamide (1) is dissolved in 2 mL methanol and treated with 5 mL methylamine (33% in ethanol). The reaction mixture is stirred at room temperature over night and all volatiles are removed in vacuo. The product is used without further purification in the next step. ESI-MS m/z 231 [M+H]+.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08623627B2uspto-grants-2014_01