반응식
C(OC(=O)[NH:7][C:8]1[N:9]([CH3:26])[N:10]=[C:11]2[C:16]=1[CH2:15][CH2:14][CH2:13][N:12]2[C:17]1[C:22]([CH3:23])=[CH:21][C:20]([CH3:24])=[CH:19][C:18]=1[Cl:25])(C)(C)C.FC(F)(F)C(O)=O>ClCCl>[Cl:25][C:18]1[CH:19]=[C:20]([CH3:24])[CH:21]=[C:22]([CH3:23])[C:17]=1[N:12]1[CH2:13][CH2:14][CH2:15][C:16]2=[C:8]([NH2:7])[N:9]([CH3:26])[N:10]=[C:11]12참가 물질
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a 0° C. solution of 287 mg of [7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridin-3-yl]carbamic acid tert-butyl ester (Example 8c) in 9 mL of dichloromethane, was added 3 mL of trifluoroacetic acid. After 15 min, the cooling bath was removed and the reaction mixture was allowed to stir and warm to room temperature during 3 h. The reaction mixture was then diluted with dichloromethane and washed with dilute aqueous sodium hydroxide. The aqueous phase was washed with additional dichloromethane, after which the combined organics were dried with magnesium sulfate and concentrated. The residue was chromatographed on silica gel eluting with a methanol/dichloromethane gradient to provide 182 mg of 7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridin-3-ylamine, mp 234-236° C.
후처리
- customthe cooling bath was removed
- additionThe reaction mixture was then diluted with dichloromethane
- washwashed with dilute aqueous sodium hydroxide
- washThe aqueous phase was washed with additional dichloromethane
- dry with materialafter which the combined organics were dried with magnesium sulfate
- concentrationconcentrated
- customThe residue was chromatographed on silica gel eluting with a methanol/dichloromethane gradient
출처 및 근거
- ORD 기록
- ord-3cbaaaa7e1f54954a9d679f76908f440
- 출처 데이터셋
- uspto-grants-2007_09
- 특허 번호
- US07268146B2
연결된 노트
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