Dimethylformamide → (5-Bromo-thiophen-2-yl)-{[1-(3,4-difluoro-benzyl)-2-oxo-1,2-dihydro-pyridine-3-carbonyl]-amino}-acetic acid methyl ester

HRID 1625477노트

반응식

HRID 1625477 반응식
[CH3:1][O:2][C:3](=[O:29])[CH:4]([NH:10][C:11]([C:13]1[C:14](=[O:28])[N:15]([CH2:19][C:20]2[CH:25]=[CH:24][C:23]([F:26])=[C:22]([F:27])[CH:21]=2)[CH:16]=[CH:17][CH:18]=1)=[O:12])[C:5]1[S:6][CH:7]=[CH:8][CH:9]=1.CN(C)C=O.[Br:35]N1C(=O)CCC1=O>>[CH3:1][O:2][C:3](=[O:29])[CH:4]([C:5]1[S:6][C:7]([Br:35])=[CH:8][CH:9]=1)[NH:10][C:11]([C:13]1[C:14](=[O:28])[N:15]([CH2:19][C:20]2[CH:25]=[CH:24][C:23]([F:26])=[C:22]([F:27])[CH:21]=2)[CH:16]=[CH:17][CH:18]=1)=[O:12]

참가 물질

4

실험 절차

{[1-(3,4-Difluoro-benzyl)-2-oxo-1,2-dihydro-pyridine-3-carbonyl]-amino}-thiophen-2-yl-acetic acid methyl ester (0.190 g, 0.000454 mol;) was dissolved in N,N-Dimethylformamide (6 mL, 0.07 mol;) and N-Bromosuccinimide (0.089 g, 0.00050 mol;) was added. The reaction was allowed to stir at room temperature o/n. LC-MS showed the formation of product at 1.89 498.45. The reaction was concentrated and dissolved in ethyl acetate. The reaction was then washed 1× with saturated bicarbonate and 1× with brine before drying with magnesium sulfate and concentrating. The crude was then dissolved in methylene chloride and injected onto the combiflash and eluted using a 0-100% hexanes ethyl acetate gradient. The pure fractions were combined and concentrated to give the product. ES (+) MS m/e=498.45

후처리

  1. concentrationThe reaction was concentrated
  2. dissolutiondissolved in ethyl acetate
  3. washThe reaction was then washed 1× with saturated bicarbonate and 1× with brine
  4. dry with materialbefore drying with magnesium sulfate
  5. concentrationconcentrating
  6. dissolutionThe crude was then dissolved in methylene chloride
  7. washeluted
  8. concentrationconcentrated
  9. customto give the product

출처 및 근거

ORD 기록
ord-7c1b32dc42614930ac3addce13df35f3
출처 데이터셋
uspto-grants-2014_07
특허 번호
US08778977B2

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