Oxalyl chloride → 3-Bromo-1-(4-methylphenyl)piperazine 2,2-dimethylpropan-1-one

HRID 417990

반응식

HRID 417990 반응식
[Br:1][CH2:2][C:3]([CH3:8])([CH3:7])[C:4](O)=[O:5].C(Cl)(=O)C(Cl)=O.Cl.Cl.[CH3:17][C:18]1[CH:23]=[CH:22][C:21]([N:24]2[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]2)=[CH:20][CH:19]=1.CCN(C(C)C)C(C)C>C(Cl)Cl>[Br:1][CH:26]1[NH:27][CH2:28][CH2:29][N:24]([C:21]2[CH:20]=[CH:19][C:18]([CH3:17])=[CH:23][CH:22]=2)[CH2:25]1.[CH3:2][C:3]([CH3:8])([CH3:7])[CH:4]=[O:5]

참가 물질

6

실험 절차

3-Bromo-2,2-dimethylpropionic acid (10.0 g, 55.3 mmol) was dissolved in DCM (60 mL). Oxalyl chloride (7.20 mL, 82.9 mmol) was added slowly over 10 minutes. The reaction mixture was stirred at room temperature for 18 hours and then concentrated in vacuo. The residue was dissolved in DCM (40 mL) and added to a solution of 4-methylphenyl-piperazine dihydrochloride (13.76 g, 55.3 mmol) and DIPEA (33.0 mL, 193.4 mmol) in DCM (100 mL) at 0° C. The reaction mixture was allowed to warm to room temperature over 1 hour and then stirred at room temperature for 16 hours. The reaction mixture was washed with 10% citric acid solution (2×100 mL), dried (MgSO4) and concentrated in vacuo to give 3-bromo-1-(4-methylphenyl)piperazine-2,2-dimethylpropan-1-one (9.62 g, 52%) as a white solid which was used without further purification.

후처리

  1. concentrationconcentrated in vacuo
  2. dissolutionThe residue was dissolved in DCM (40 mL)
  3. temperatureto warm to room temperature over 1 hour
  4. stirringstirred at room temperature for 16 hours
  5. washThe reaction mixture was washed with 10% citric acid solution (2×100 mL)
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-43dd9f090fc14470b0593744eb01787f
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08093248B2

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