Hydrochloric Acid → (10,11-Dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-10-yl)-[4-(3-hydroxy-cyclohex-1-en-1-yl)-phenyl]-methanone
반응식
[CH:1]1[CH:2]=[CH:3][N:4]2[CH2:10][C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[N:7]([C:15]([C:17]3[CH:22]=[CH:21][C:20]([C:23]4[CH2:28][CH2:27][CH2:26][C:25](=[O:29])[CH:24]=4)=[CH:19][CH:18]=3)=[O:16])[CH2:6][C:5]=12.[Cl-].[Ce+3].[Cl-].[Cl-].[BH4-].[Na+].[H][H].Cl>CO.C(OCC)C>[CH:1]1[CH:2]=[CH:3][N:4]2[CH2:10][C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[N:7]([C:15]([C:17]3[CH:18]=[CH:19][C:20]([C:23]4[CH2:28][CH2:27][CH2:26][CH:25]([OH:29])[CH:24]=4)=[CH:21][CH:22]=3)=[O:16])[CH2:6][C:5]=12참가 물질
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
3-[4-(10,11-Dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-10-carbonyl)-phenyl]-cyclohex-2-enone of Example 24 (0.100 g, 0.261 mmol) and cerium (III) chloride (0.064 g, 0.261 mmol) were dissolved in methanol (1.3 mL) followed by addition of solid sodium borohydride (0.010 g, 0.261 mmol). After hydrogen evolution ceased (approximately 5 minutes), 0.1 N hydrochloric acid (50 mL) was added and the resulting mixture extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, filtered and concentrated. A slightly yellow solid was isolated which was dissolved in boiling diethyl ether and filtered. The product was precipitated from the filtrate by addition of pentane and the precipitate filtered and dried to afford the title compound (0.100 g) as an amorphous white solid.
후처리
- additionwas added
- extractionthe resulting mixture extracted with ethyl acetate
- dry with materialThe extract was dried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customA slightly yellow solid was isolated which
- dissolutionwas dissolved
- filtrationfiltered
- customThe product was precipitated from the filtrate by addition of pentane
- filtrationthe precipitate filtered
- customdried
출처 및 근거
- ORD 기록
- ord-5f36afab113842339506369e8350a84b
- 출처 데이터셋
- uspto-grants-2006_04
- 특허 번호
- US07022699B2
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