Triethylamine → Ethyl 2-(difluoromethyl)-5-(isobutyramidomethyl)nicotinate

HRID 241441노트

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HRID 241441 반응식
Cl.Cl.[NH2:3][CH2:4][C:5]1[CH:6]=[C:7]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:8]([CH:11]([F:13])[F:12])=[N:9][CH:10]=1.C(N(CC)CC)C.[C:26](Cl)(=[O:30])[CH:27]([CH3:29])[CH3:28]>C(Cl)Cl>[F:12][CH:11]([F:13])[C:8]1[C:7]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:6][C:5]([CH2:4][NH:3][C:26](=[O:30])[CH:27]([CH3:29])[CH3:28])=[CH:10][N:9]=1

참가 물질

5

실험 절차

Cool a mixture of ethyl 5-(aminomethyl)-2-(difluoromethyl)pyridine-3-carboxylate dihydrochloride (29.8 g, 111.8 mmol, 1.0 equiv), DCM (510 mL), and triethylamine (59.2 mL, 424.6 mmol, 3.8 equiv) to 0° C., then add a solution of isobutyryl chloride (15.3 mL, 145.3 mmol, 1.3 equiv) in DCM (23 mL) drop wise over 20 min. Stir overnight while allowing the mixture to warm to room temperature. Remove the solid precipitate by filtration, and rinse the filter with EtOAc (500 mL). Concentrate the filtrate under reduced pressure; filter the concentrate to remove the solids; and rinse the solids with EtOAc. Concentrate the filtrate under reduced pressure to give a yellow oil. Subject this crude material to silica gel chromatography eluting with a gradient of 40-90% EtOAc/hexanes gradient, to give the title compound as a light yellow crystalline solid (25.8 g, 77% yield). ES/MS (m/z) 301 (M+1).

후처리

  1. temperatureCool
  2. customRemove the solid precipitate
  3. filtrationby filtration
  4. washrinse the
  5. filtrationfilter with EtOAc (500 mL)
  6. concentrationConcentrate the filtrate under reduced pressure
  7. filtrationfilter the
  8. concentrationconcentrate
  9. customto remove the solids
  10. washand rinse the solids with EtOAc
  11. concentrationConcentrate the filtrate under reduced pressure
  12. customto give a yellow oil
  13. washeluting with a gradient of 40-90% EtOAc/hexanes gradient

출처 및 근거

ORD 기록
ord-6da8dc3c62d340669ebf0dde28cb8623
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08648200B2

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