반응식
C([O:3][C:4]([CH2:6][O:7][CH:8]1[C:14]2[CH:15]=[C:16]([Cl:19])[CH:17]=[CH:18][C:13]=2[N:12]([C:20](=[O:37])[C:21]2[CH:26]=[CH:25][C:24]([NH:27][C:28](=[O:36])[C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=3[CH3:35])=[CH:23][CH:22]=2)[CH2:11][CH2:10][CH2:9]1)=O)C.[BH4-].[Li+].Cl>O1CCCC1>[OH:3][CH2:4][CH2:6][O:7][CH:8]1[C:14]2[CH:15]=[C:16]([Cl:19])[CH:17]=[CH:18][C:13]=2[N:12]([C:20](=[O:37])[C:21]2[CH:26]=[CH:25][C:24]([NH:27][C:28](=[O:36])[C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=3[CH3:35])=[CH:23][CH:22]=2)[CH2:11][CH2:10][CH2:9]1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 5-ethoxycarbonylmethoxy-7-chloro-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (2.2 g) in tetrahydrofuran (50 ml) is added with stirring lithium borohydride (0.28 g) at room temperature, and the mixture is refluxed for 30 minutes. The reaction solution is poured into diluted hydrochloric acid and extracted with dichloromethane. The extract is dried over magnesium sulfate and the solvent is distilled off under reduced pressure. The resulting residue is purified by silica gel column chromatography (eluent; dichloromethane:methanol=100:1→50:1), and recrystallized from dichloromethane/diethyl ether to give 5-(2-hydroxyethoxy)-7-chloro-1-[4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (1.6 g) as white powder, mp. 185°-187.5° C.
후처리
- temperaturethe mixture is refluxed for 30 minutes
- extractionextracted with dichloromethane
- dry with materialThe extract is dried over magnesium sulfate
- distillationthe solvent is distilled off under reduced pressure
- customThe resulting residue is purified by silica gel column chromatography (eluent; dichloromethane:methanol=100:1→50:1)
- customrecrystallized from dichloromethane/diethyl ether
출처 및 근거
- ORD 기록
- ord-afa3792d8ff0460690d319722a9ee47e
- 출처 데이터셋
- uspto-grants-1993_09
- 특허 번호
- US05244898
연결된 노트
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