반응 #80205

ord-9966b6b3fb934e508c6f4ea6101b2d21

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
  5. 5
    기타to provide a residue
  6. 6
    기타This material was purified by preparative thin-layer-chromatography on silica eluting with ethyl acetate
  7. 7
    workup.ADDITIONThe product containing band
  8. 8
    기타was collected
  9. 9
    세척eluted with 5% methanol in ethyl acetate

실험 절차

7-[(4′-Trifluoromethyl-biphenyl-2-carbonyl)-amino]-quinoline-3-carboxylic acid (100 mg, 0.23 mmol) was combined with phenylalaninamide (38 mg, 0.23 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (53 mg, 0.27 mmol), 1-hydroxybenzotriazole (34 mg, 0.25 mmol), and triethylamine (0.13 ml, 0.92 mmol) in 1.5 ml of dichloromethane. After stirring overnight at ambient temperature, the reaction mixture was diluted with 50 ml of dichloromethane, and the organic phase washed sequentially with water, and brine, and then dried over anhydrous magnesium sulfate, filtered and concentrated under vacuum to provide a residue. This material was purified by preparative thin-layer-chromatography on silica eluting with ethyl acetate. The product containing band was collected and eluted with 5% methanol in ethyl acetate to afford 47 mg of the title compound.

출처

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