Phenacyl bromide → Tert-butyl 4-methyl-3-(4-phenylthiazol-2-yl)piperazine-1-carboxylate

HRID 874969노트

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HRID 874969 반응식
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=O.[C:11]([CH:14]1[N:19]([CH3:20])[CH2:18][CH2:17][N:16]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:15]1)(=[S:13])[NH2:12]>CCO>[CH3:20][N:19]1[CH2:18][CH2:17][N:16]([C:21]([O:23][C:24]([CH3:27])([CH3:25])[CH3:26])=[O:22])[CH2:15][CH:14]1[C:11]1[S:13][CH:2]=[C:3]([C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)[N:12]=1

참가 물질

4

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온도
70 °C

실험 절차

A mixture of 2-bromoacetophenone (130 mg, 0.65 mmol) and tert-butyl 3-carbamothioyl-4-methylpiperazine-1-carboxylate (170 mg, 0.65 mmol) in EtOH (15 mL) was heated to 70° C. for 4 h. The reaction mixture was cooled to room temperature and solvent was evaporated under reduced pressure. The residue was diluted with water and the organic product was extracted with EtOAc. The combined extracts were washed with H2O and brine, and concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel 60-120 mesh, eluent 20-25% EtOAc in petroleum ether) to afford tert-butyl 4-methyl-3-(4-phenylthiazol-2-yl)piperazine-1-carboxylate (150 mg, yield 64%). 1H NMR (300 MHz, CDCl3) δ 7.92-7.90 (m, 2H), 7.49 (m, 1H), 7.46-7.41 (m, 2H), 7.37-7.34 (m, 1H), 4.03-3.98 (m, 1H), 3.67-3.64 (m, 2H), 3.23-3.15 (m, 2H), 2.97-2.93 (m, 2H), 2.26 (s, 3H), 1.46 (s, 9H). MS (ESI) m/z: Calculated for C19H25N3O2S: 359.17. found: 360.2 (M+H)+

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customsolvent was evaporated under reduced pressure
  3. additionThe residue was diluted with water
  4. extractionthe organic product was extracted with EtOAc
  5. washThe combined extracts were washed with H2O and brine
  6. concentrationconcentrated under reduced pressure
  7. customThe crude product was purified by column chromatography (silica gel 60-120 mesh, eluent 20-25% EtOAc in petroleum ether)

출처 및 근거

ORD 기록
ord-48d68d5e72474c058cf12631ab5ea7cc
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08981084B2

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