반응 #578412

ord-4b1c936e05794d15a800e31f39b0a2de

반응 방정식

FC(F)(F)c1cc(Br)ccc1Cl
4-bromo-1-chloro-2-(trifluoromethyl)benzene
Cc1cnc(Cl)nc1N
4-amino-2-chloro-5-methylpyrimidine
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
Cc1cnc(Cl)nc1Nc1ccc(Cl)c(C(F)(F)F)c1
2-chloro-N-(4-chloro-3-(trifluoromethyl)phenyl)-5-methylpyrimidin-4-amine
수율 62.1%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도under refluxed for 10 h under argon
  3. 3
    기타The solvent was removed
  4. 4
    기타the residue was purified by HPLC

실험 절차

A mixture of 4-bromo-1-chloro-2-(trifluoromethyl)benzene (259 mg, 1.0 mmol), 4-amino-2-chloro-5-methylpyrimidine (143 mg, 1.0 mmol), Pd2(dba)3 (9 mg, 0.01 mmol), xantphos (14 mg, 0.02 mmol) and cesium carbonate (650 mg, 2.0 mmol) in dioxane (15 mL) was heated under refluxed for 10 h under argon. The solvent was removed and the residue was purified by HPLC to give an intermediate 2-chloro-N-(4-chloro-3-(trifluoromethyl)phenyl)-5-methylpyrimidin-4-amine as brown solid (200 mg, 62%). A mixture of this intermediate (161 mg, 0.5 mmol) and 4-(2-(pyrrolidin-1-yl)ethoxy)benzenamine (103 mg, 0.5 mmol) in glacial acetic acid (5 mL) was heated under refluxed for 3 h under argon. The crude reaction mixture on purification using HPLC gave the title compound as brown solid (75 mg, 31%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07528143B2uspto-grants-2009_05