반응식
Cl[CH2:2][C:3]([NH:5][C:6]1[C:11]([CH3:12])=[CH:10][CH:9]=[CH:8][C:7]=1[CH3:13])=[O:4].[CH3:14][C:15]1([CH3:28])[N:19]2[CH2:20][CH2:21][NH:22][CH2:23][CH:18]2[C:17](=[O:24])[N:16]1[CH:25]([CH3:27])[CH3:26].C(N(CC)CC)C>CN(C)C=O>[CH3:13][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]([CH3:12])[C:6]=1[NH:5][C:3](=[O:4])[CH2:2][N:22]1[CH2:21][CH2:20][N:19]2[C:15]([CH3:14])([CH3:28])[N:16]([CH:25]([CH3:26])[CH3:27])[C:17](=[O:24])[CH:18]2[CH2:23]1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 75 °C
실험 절차
A mixture of 8.2 parts of 2-chloro-N-(2,6-dimethylphenyl)acetamide, 7.2 parts of hexahydro-3,3-dimethyl-2-(1-methylethyl)imidazo[1,5-a]pyrazin-1(5H)-one, 7 parts of N,N-diethylethanamine and 54 parts of N,N-dimethylformamide was stirred and heated for 3 hours at 75° C. After cooling to 0° C., the precipitate was filtered off and the filtrate was evaporated. The residue was dissolved in 300 parts of trichloromethane. This solution was washed with 50 parts of water, dried, filtered and evaporated. The residue was triturated in 2,2'-oxybispropane. After cooling to 0° C., the product was filtered off and dried, yielding 9.2 parts (72.7%) of N-(2,6-dimethylphenyl)hexahydro-3,3-dimethyl-2-(1-methylethyl)-1-oxoimidazo[1,5-a]pyrazine-7(8H)-acetamide; mp. 155° C. (intermediate 101).
후처리
- temperatureAfter cooling to 0° C.
- filtrationthe precipitate was filtered off
- customthe filtrate was evaporated
- dissolutionThe residue was dissolved in 300 parts of trichloromethane
- washThis solution was washed with 50 parts of water
- customdried
- filtrationfiltered
- customevaporated
- customThe residue was triturated in 2,2'-oxybispropane
- temperatureAfter cooling to 0° C.
- filtrationthe product was filtered off
- customdried
출처 및 근거
- ORD 기록
- ord-aefb654b87b7431f99ffecb3fefb8341
- 출처 데이터셋
- uspto-grants-1988_08
- 특허 번호
- US04766125
연결된 노트
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