반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([C:14]([NH:16][C:17]3[CH:37]=[CH:36][C:20]([C:21]([N:23]([CH3:35])[C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=4[C:30](OCC)=[O:31])=[O:22])=[CH:19][CH:18]=3)=[O:15])=[CH:10][CH:11]=[CH:12][CH:13]=2)=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.Cl>O1CCCC1>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:9]([C:14]([NH:16][C:17]3[CH:18]=[CH:19][C:20]([C:21]([N:23]([CH3:35])[C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=4[CH2:30][OH:31])=[O:22])=[CH:36][CH:37]=3)=[O:15])=[CH:10][CH:11]=[CH:12][CH:13]=2)=[CH:6][CH:7]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
A solution of 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-ethoxycarbonylphenyl)benzamide (493 mg) in tetrahydrofuran (20 ml) was cooled in an ice bath. Lithium aluminum hydride (1M solution in tetrahydrofuran, 2.5 ml) was added dropwise to the solution and the mixture was stirred at the same temperature for 2 hours. Water was slowly added to the solution and resulting mixture was acidified with 1N hydrochloric acid. The solution was extracted with chloroform and the organic solution was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was subjected to silica gel column (20 g, 2% methanol in chloroform). The product was solidified with diethyl ether to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-hydroxymethylphenyl)benzamide (245 mg) as a white powder.
후처리
- customresulting mixture
- extractionThe solution was extracted with chloroform
- washthe organic solution was washed with water and brine
- dry with materialdried over magnesium sulfate
- customThe solvent was evaporated in vacuo
출처 및 근거
- ORD 기록
- ord-deb1367bff014b7691c7277433338c96
- 출처 데이터셋
- uspto-grants-2001_04
- 특허 번호
- US06211242B1
연결된 노트
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