Dimethylformamide → Tert-butyl 4-(2-fluoro-3-formylbenzoyl)piperazine-1-carboxylate

HRID 1172452노트

반응식

HRID 1172452 반응식
Br[C:2]1[C:3]([F:23])=[C:4]([CH:20]=[CH:21][CH:22]=1)[C:5]([N:7]1[CH2:12][CH2:11][N:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:9][CH2:8]1)=[O:6].C([Mg]Cl)C(C)C.CN(C)[CH:32]=[O:33].[Cl-].[NH4+]>O1CCCC1>[F:23][C:3]1[C:2]([CH:32]=[O:33])=[CH:22][CH:21]=[CH:20][C:4]=1[C:5]([N:7]1[CH2:12][CH2:11][N:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:9][CH2:8]1)=[O:6]

참가 물질

6

실험 절차

194 mg of tert-butyl 4-(3-bromo-2-fluorobenzoyl)piperazine-1-carboxylate was dissolved in 5.0 ml of tetrahydrofuran, and 1.25 ml of a solution of isobutyl magnesium chloride in tetrahydrofuran (2.0 M) was added thereto at −78° C. After stirring at the same temperature for 2 hours, 0.39 ml (5.0 mmol) of N,N-dimethylformamide was added thereto. The resulting mixture was stirred at the same temperature for 30 minutes and further stirred at 0° C. for 30 minutes. To the reaction mixture was added saturated ammonium chloride, and the mixture was extracted with chloroform. The organic layer was washed with brine and then concentrated. The residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate=9/1 to 1/1) to give the title compound.

후처리

  1. customat −78° C
  2. stirringThe resulting mixture was stirred at the same temperature for 30 minutes
  3. stirringfurther stirred at 0° C. for 30 minutes
  4. extractionthe mixture was extracted with chloroform
  5. washThe organic layer was washed with brine
  6. concentrationconcentrated
  7. customThe residue was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate=9/1 to 1/1)

출처 및 근거

ORD 기록
ord-8101c7d7376a4209950002c7019f1b76
출처 데이터셋
uspto-grants-2010_11
특허 번호
US07834018B2

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