Dichloromethane → HCID 69275389, 화합물

HRID 2375382노트

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HRID 2375382 반응식
[C:1]([C:4]1[CH:8]=[C:7]([CH3:9])[N:6]([C:10]2[CH:15]=[CH:14][C:13]([O:16]C)=[CH:12][C:11]=2[O:18][CH3:19])[C:5]=1[CH3:20])(=[O:3])[CH3:2].B(Br)(Br)Br.C(Cl)Cl>>[C:1]([C:4]1[CH:8]=[C:7]([CH3:9])[N:6]([C:10]2[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][C:11]=2[O:18][CH3:19])[C:5]=1[CH3:20])(=[O:3])[CH3:2]

참가 물질

4

실험 절차

To a solution of 3-acetyl-1-(2,4-dimethoxyphenyl)-2,5-dimethylpyrrole (2.73 g, 10 mmol) (EXAMPLE 33) in CH2Cl2at rt (75 mL) was added a 1.0M solution of boron tribromide in CH2Cl2 (15 mL, 15 mmol) and the reaction monitored by LC. After complete consumption of the starting material, the reaction was carefully quenched with saturated NaHCO3 and partitioned between EtOAc and water. The organic layer was washed with brine, dried over MgSO4, filtered, concentrated in vacuo, and purified by flash chromatography to give 3-acetyl-2,5-dimethyl-1-(4-hydroxy-2-methoxyphenyl)pyrrole as a tan solid: 1H NMR (CDCl3, 500 MHz) δ 6.92 (d, 1H), 6.61 (d, 1H), 6.54 (dd, 1H), 6.32 (s, 1H), 3.72 (s, 3H), 2.44 (s, 3H), 2.26 (s, 3H), 1.93 (s, 3H), 1.69 (br s, 1H); MS (ESI) 260 (M+H)+.

후처리

  1. customAfter complete consumption of the starting material
  2. customthe reaction was carefully quenched with saturated NaHCO3
  3. custompartitioned between EtOAc and water
  4. washThe organic layer was washed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. custompurified by flash chromatography

출처 및 근거

ORD 기록
ord-ee4b61021eb24c619151a261c472286c
출처 데이터셋
uspto-grants-2008_12
특허 번호
US07465730B2

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