Acetyl chloride → 3-Acetylaminopyrazole
반응식
[NH:1]1[C:5]([NH2:6])=[CH:4][CH:3]=[N:2]1.CN1CC[O:11][CH2:10][CH2:9]1.C(Cl)(=O)C.[OH-].[Na+]>C(Cl)Cl>[NH:1]1[C:5]([NH:6][C:10](=[O:11])[CH3:9])=[CH:4][CH:3]=[N:2]1참가 물질
6
실험 절차
To a solution of 1H-pyrazol-5-amine (50 g, 0.602 mol) and N-methylmorpholine (160 mL, 1.44 mol) in CH2Cl2 (2 L) was added acetyl chloride (99 mL, 1.38 mol) dropwise at 0° C. under an atmosphere of nitrogen. The reaction mixture was stirred at room temperature for 1 d. Some di-acylated product was observed in an LCMS. The reaction mixture was concentrated in vacuo and the resulting solid was suspended in MeOH (2 L) and cooled to 0° C. 4 M NaOH solution (aq., 440 mL, 1.75 mol) was added slowly and the mixture allowed to warm to room temperature over 1.5 h. The MeOH was removed in vacuo and the solid was collected by filtration, washed with minimal cold water and dried in vacuo to provide the title compound as a solid (60 g).
후처리
- concentrationThe reaction mixture was concentrated in vacuo
- temperaturecooled to 0° C
- temperatureto warm to room temperature over 1.5 h
- customThe MeOH was removed in vacuo
- filtrationthe solid was collected by filtration
- washwashed with minimal cold water
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-9ec5f41752d848a9b9d8d94217ee8533
- 출처 데이터셋
- uspto-grants-2016_06
- 특허 번호
- US09371332B2
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