반응식
[Cl:1][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=2)=[CH:6][CH:7]=1.Cl.Cl.[NH2:20][CH:21]1[CH2:26][CH2:25][CH2:24][NH:23][CH2:22]1.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[ClH:1].[F:15][C:14]([F:17])([F:16])[C:11]1[CH:12]=[CH:13][C:8]([C:5]2[N:4]=[N:3][C:2]([N:23]3[CH2:24][CH2:25][CH2:26][CH:21]([NH2:20])[CH2:22]3)=[CH:7][CH:6]=2)=[CH:9][CH:10]=1참가 물질
반응 조건
- 온도
- 120 °C
실험 절차
3-Chloro-6-(4-trifluoromethylphenyl)pyridazine (0.2 g, 0.77 mmol), 3-aminopiperidine dihydrochloride (0.27 g, 1.54 mmol) and potassium carbonate (0.53 g, 3.87 mmol) were mixed in acetone (4 mL) in a 20 mL microwave vessel. The reaction mixture was heated in a microwave oven for 2 h at 120° C. The reaction mixture was filtered and the precipitate was washed with MeOH. The combined organic phases were evaporated. The crude oil was purified on a silicagel column (0.04-0.063 mesh) using dichloromethane/MeOH (9:1) as eluent. This afforded 110 mg of a oil that was dissolved in MeOH and acidified with concentrated HCl (5 mL). The mixture was evaporated and the residue was dissolved in MeOH (1 mL) and ether (100 mL) was added with stirring. The mixture was evaporated to give 76 mg (25%) of the title compound as a yellow solid.
후처리
- filtrationThe reaction mixture was filtered
- washthe precipitate was washed with MeOH
- customThe combined organic phases were evaporated
- customThe crude oil was purified on a silicagel column (0.04-0.063 mesh)
- dissolutionThis afforded 110 mg of a oil that was dissolved in MeOH
- customThe mixture was evaporated
- dissolutionthe residue was dissolved in MeOH (1 mL)
- additionether (100 mL) was added
- customThe mixture was evaporated
출처 및 근거
- ORD 기록
- ord-fee32dfc11fb4f769ef6a6273104e86b
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08846677B2
연결된 노트
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