反应 #40362

ord-148cb1d56fd049cf839a5bc3d69b3e2b

反应方程式

Cc1cc(Oc2ccnc(Oc3cccc(Cl)c3C)n2)c(C)cc1N
4-[2-(3-chloro-2-methyl-phenoxy)-pyrimidin-4-yloxy]-2,5-dimethyl-phenylamine
CO
methanol
CCN(C)C(OC)OC
N-(dimethoxymethyl)-N-methyl-ethanamine
CCN(C)C=Nc1cc(C)c(Oc2ccnc(Oc3cccc(Cl)c3C)n2)cc1C
N′-{4-[2-(3-chloro-2-methyl-phenoxy)-pyrimidin-4-yloxy]-2,5-dimethyl-phenyl}-N-ethyl-N-methyl-formamidine

反应条件

温度
45°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added
  2. 2
    干燥The reaction mixture was dried over magnesium sulfate
  3. 3
    浓缩concentrated in vacuo
  4. 4
    其他yielded 290 mg (76%) with a purity of 78%

实验过程

To a mixture of 293 mg (0.7 mmol) of 4-[2-(3-chloro-2-methyl-phenoxy)-pyrimidin-4-yloxy]-2,5-dimethyl-phenylamine in 20 ml methanol 182 mg (1.05 mmol) of N-(dimethoxymethyl)-N-methyl-ethanamine (77% pure) was added. The reaction mixture was stirred for 20 hrs at 45° C. The reaction mixture was dried over magnesium sulfate concentrated in vacuo and yielded 290 mg (76%) with a purity of 78%; log P (pH 2.3)=2.08.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07727986B2uspto-grants-2010_06