Dimethylformamide → (R)-3-(5-Bromo-thiophen-2-yl)-3-{[1-(3,4-difluoro-benzyl)-2-oxo-1,2-dihydro-pyridine-3-carbonyl]-amino}-propionic acid methyl ester
반응식
[CH3:1][O:2][C:3](=[O:30])[CH2:4][C@@H:5]([NH:11][C:12]([C:14]1[C:15](=[O:29])[N:16]([CH2:20][C:21]2[CH:26]=[CH:25][C:24]([F:27])=[C:23]([F:28])[CH:22]=2)[CH:17]=[CH:18][CH:19]=1)=[O:13])[C:6]1[S:7][CH:8]=[CH:9][CH:10]=1.CN(C)C=O.[Br:36]N1C(=O)CCC1=O>C(Cl)Cl>[CH3:1][O:2][C:3](=[O:30])[CH2:4][C@H:5]([C:6]1[S:7][C:8]([Br:36])=[CH:9][CH:10]=1)[NH:11][C:12]([C:14]1[C:15](=[O:29])[N:16]([CH2:20][C:21]2[CH:26]=[CH:25][C:24]([F:27])=[C:23]([F:28])[CH:22]=2)[CH:17]=[CH:18][CH:19]=1)=[O:13]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
(R)-3-{[1-(3,4-Difluoro-benzyl)-2-oxo-1,2-dihydro-pyridine-3-carbonyl]-amino}-3-thiophen-2-yl-propionic acid methyl ester (0.420 g, 0.000971 mol;) was dissolved in N,N-Dimethylformamide (20 mL, 0.2 mol;) and N-Bromosuccinimide (0.19 g, 0.0011 mol;) was added. The reaction was allowed to stir o/n and LC-MS showed formation of product at 1.87 510.95. The reaction was diluted with methylene chloride and washed 1× with saturated bicarbonate, 1× with 5% citric acid, and 1× with brine. The organic layer was then dried with magnesium sulfate and concentrated to give the crude material. The crude was dissolved in methylene chloride and purified by combiflash 0-100% hexanes/ethyl acetate to give the pure product. ES (+) MS m/e=510.95
후처리
- washwashed 1× with saturated bicarbonate, 1× with 5% citric acid, and 1× with brine
- dry with materialThe organic layer was then dried with magnesium sulfate
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-50d20f586c42495ea9c798b7f20349bb
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08778977B2
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