반응식
[CH:1]1[S:5][C:4]([NH:6][C:7]([NH2:9])=[NH:8])=[N:3][C:2]=1[CH2:10][S:11][CH2:12][CH2:13][C:14]([NH:16][S:17]([NH2:20])(=[O:19])=[O:18])=[NH:15].[NH2:21][C@H:22]([C:27]([OH:29])=[O:28])[CH2:23][C:24]([OH:26])=[O:25]>ClCCl>[CH:1]1[S:5][C:4]([NH:6][C:7]([NH2:9])=[NH:8])=[N:3][C:2]=1[CH2:10][S:11][CH2:12][CH2:13][C:14]([NH:16][S:17]([NH2:20])(=[O:19])=[O:18])=[NH:15].[NH2:21][C@H:22]([C:27]([O-:29])=[O:28])[CH2:23][C:24]([O-:26])=[O:25]참가 물질
4
실험 절차
A mixture of 0.56 g (0.166 cmole) of famotidine and 0.222 g (0.166 cmole) of aspartic acid was suspended in dichloromethane (10 ml). The mixture was stirred for 3 hours at room temperature, was filtered, washed with dichloromethane and dried. Weight: 0.782 g. Quantitative yield. Stereoscopically homogenous white microcrystalline solid, similar to milky quartz. Slightly bitter taste. M.P.: 165°-170° C. IR FIG. 2.
후처리
- filtrationwas filtered
- washwashed with dichloromethane
- customdried
출처 및 근거
- ORD 기록
- ord-f1b01b4e29a740aa9b69fbc4007a5bb9
- 출처 데이터셋
- uspto-grants-1988_06
- 특허 번호
- US04749790
연결된 노트
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