반응 #466911

ord-5b637e7fed394ef799ad953188f659ec

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척the mixture washed consecutively with 1N aqueous HCl (50 ml×2) and saturated aqueous sodium bicarbonate (50 ml×2)
  2. 2
    건조The organic layer was dried (MgSO4) and solvent
  3. 3
    기타removed
  4. 4
    기타The resultant residue was purified by flash chromatography
  5. 5
    세척eluting with ethyl acetate/hexane (1:2)

실험 절차

To a solution of 3-amino-6-chloro-2-(3-methoxybenzoyl)indole (Example 18, 413 mg, 1.37 mmol) in dichloromethane (20 ml) was added pyridine (0.33 ml, 4.12 mmol) and acetyl chloride (0.14 ml, 2.06 mmol). After stirring for 0.5 h, water (1 ml) and diethyl ether (100 ml) were added, and the mixture washed consecutively with 1N aqueous HCl (50 ml×2) and saturated aqueous sodium bicarbonate (50 ml×2). The organic layer was dried (MgSO4) and solvent removed. The resultant residue was purified by flash chromatography eluting with ethyl acetate/hexane (1:2) to afford the title compound as an oil. Crystallization from ethanol/hexane to give 260 mg (55%) of title compound. m.p.: 161-162° C. 1H-NMR (CDCl3) δ: 9.92 (1H, br s), 8.32 (1H, br s), 8.22 (1H, d, J=9.2 Hz), 7.47 (1H, dd, J=7.7 and 8.1 Hz), 7.37-7.26 (3H, m), 7.18-7.08 (1H, m), 7.10 (1H, dd, J=1.6 and 9.0 Hz), 3.88 (3H, s), 2.25 (3H, s)

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06300363B1uspto-grants-2001_10