반응 #80227

ord-b4f22c5ba3ce4586adf6677244390434

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척the organic phase washed sequentially with water, and brine
  2. 2
    건조dried over anhydrous magnesium sulfate
  3. 3
    여과filtered
  4. 4
    농축concentrated under vacuum

실험 절차

7-[(4′-Trifluoromethyl-biphenyl-2-carbonyl)-amino]-quinoline-3-carboxylic acid (50 mg, 0.11 mmol) was combined with 3-methoxybenzylamine (16 mg, 0.11 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (26 mg, 0.14 mmol), 1-hydroxybenzotriazole (17 mg, 0.13 mmol), and triethylamine (0.064 ml, 0.46 mmol) in 1 ml of dichloromethane. After stirring overnight at ambient temperature, the reaction mixture was diluted with 30 ml of ethyl acetate, and the organic phase washed sequentially with water, and brine, and then dried over anhydrous magnesium sulfate, filtered and concentrated under vacuum to afford 53 mg of the title compound as a colorless solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06713489B2uspto-grants-2004_03