반응 #42057

ord-b7f582fc8d244fbdb46b0a45b6b458da

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도Under ice-cool
  2. 2
    workup.STIRRINGAfter stirring for 1 hour
  3. 3
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  4. 4
    workup.ADDITIONdiluted with water
  5. 5
    추출followed by extraction with ethyl acetate twice
  6. 6
    건조dried over anhydrous magnesium sulfate
  7. 7
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  8. 8
    기타the residue was purified by silica gel column chromatography

실험 절차

1.04 g of 2,4-diaminotoluene, 104 mg of 4-(dimethylamino)pyridine and 4.9 ml of N,N-diisopropyl-N-ethylamine were dissolved in 40 ml of acetonitrile. Under ice-cool stirring, 3.70 g of 4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoyl chloride dihydrochloride (Reference Example 2) was added by four portions. After stirring for 1 hour, the solvent was distilled off under reduced pressure and diluted with water. The reaction solution was alkalified with an aqueous saturated sodium hydrogen carbonate solution, followed by extraction with ethyl acetate twice, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography to obtain 2.56 g of the objective compound as a pale brown amorphous.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07728131B2uspto-grants-2010_06