5-methyl-4-oxo-4,5,6,7-tetrahydro-2H-pyrrolo[3,4-c]pyridine-1-carbaldehyde → 5-Methyl-1-(2-oxo-4-piperidin-4-yl-1,2-dihydroindol-3-ylidene-methyl)-2,5,6,7-tetrahydro-pyrrolo[3,4-c]pyridin-4-one
반응식
[NH:1]1[CH2:6][CH2:5][CH:4]([C:7]2[CH:15]=[CH:14][CH:13]=[C:12]3[C:8]=2[CH2:9][C:10](=[O:16])[NH:11]3)[CH2:3][CH2:2]1.[CH3:17][N:18]1[CH2:23][CH2:22][C:21]2=[C:24]([CH:27]=O)[NH:25][CH:26]=[C:20]2[C:19]1=[O:29]>N1CCCCC1.C(O)C>[CH3:17][N:18]1[CH2:23][CH2:22][C:21]2=[C:24]([CH:27]=[C:9]3[C:8]4[C:12](=[CH:13][CH:14]=[CH:15][C:7]=4[CH:4]4[CH2:3][CH2:2][NH:1][CH2:6][CH2:5]4)[NH:11][C:10]3=[O:16])[NH:25][CH:26]=[C:20]2[C:19]1=[O:29]참가 물질
5
반응물 2
생성물 1
시약·촉매·용매 2
실험 절차
A mixture of 4-piperidin-4-yl-1,3-dihydroindol-2-one (58.4 mg, 0.27 mmol), 5-methyl-4-oxo-4,5,6,7-tetrahydro-2H-pyrrolo[3,4-c]pyridine-1-carbaldehyde (48 mg, 0.27 mmol) and piperidine (1 drop) in ethanol (1 mL) was stirred at room temperature for 7 days. The precipitate was collected by vacuum filtration, washed with ethanol and dried to give 58 mg (57%) of the title compound as a yellow solid.
후처리
- filtrationThe precipitate was collected by vacuum filtration
- washwashed with ethanol
- customdried
출처 및 근거
- ORD 기록
- ord-5953f9e269d345c7b5c12457f06ec8c7
- 출처 데이터셋
- uspto-grants-2003_10
- 특허 번호
- US06635640B2
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