반응식
[NH2:1][C:2]1[C:3](=[O:28])[N:4]([CH2:14][C:15]([NH:17][CH:18]([CH:25]([CH3:27])[CH3:26])[C:19](=[O:24])[C:20]([F:23])([F:22])[F:21])=[O:16])[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:6][CH:7]=1.ON1C2C=CC=CC=2N=N1.[C:39](O)(=[O:43])[C:40]([CH3:42])=[O:41].COC1C=CC(CC(O)=O)=CC=1>CN(C)C1C=CN=CC=1.ClCCl.O1CCCC1>[O:28]=[C:3]1[C:2]([NH:1][C:39](=[O:43])[C:40]([CH3:42])=[O:41])=[CH:7][CH:6]=[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:4]1[CH2:14][C:15]([NH:17][CH:18]([CH:25]([CH3:26])[CH3:27])[C:19](=[O:24])[C:20]([F:22])([F:23])[F:21])=[O:16]참가 물질
8
반응물 4
생성물 1
시약·촉매·용매 3
실험 절차
2-(3-Amino-2-oxo-6-phenyl-1,2-dihydro-1-pyridyl)-N-(3,3,3-trifluoro-1-isopropyl-2-oxopropyl)acetamide was subjected to procedure similar to Acylation Method B, but substituting: dichloromethane for tetrahydrofuran, 4-dimethylaminopyridine for 1-hydroxybenzotriazole, and pyruvic acid for 4-methoxyphenyl acetic acid. After 72 h, dichloromethane was added and the mixture was washed (water, brine), dried (magnesium sulfate) and evaporated. Chromatography, eluting with dichloromethane:methanol (gradient, 99.5:0.5, 99:1), gave the title compound as a pale yellow solid; TLC: Rf =0.44, dichloromethane:methanol (98:2); MS: m/z=466(M+1).
후처리
- washthe mixture was washed (water, brine)
- dry with materialdried (magnesium sulfate)
- customevaporated
- washChromatography, eluting with dichloromethane
출처 및 근거
- ORD 기록
- ord-6ed4f2edb3374584b7c18a037ad329ed
- 출처 데이터셋
- uspto-grants-1996_05
- 특허 번호
- US05521179
연결된 노트
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