Acetic Acid → N-(5-chloropyridin-2-yl)-5-iodo-2-[(1-isopropylpiperidin-4-ylcarbonyl)amino]benzamide

HRID 1247141노트

반응식

HRID 1247141 반응식
F[C:2](F)(F)[C:3](O)=O.[Cl:8][C:9]1[CH:10]=[CH:11][C:12]([NH:15][C:16](=[O:33])[C:17]2[CH:22]=[C:21]([I:23])[CH:20]=[CH:19][C:18]=2[NH:24][C:25]([CH:27]2[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]2)=[O:26])=[N:13][CH:14]=1.[C:34](O)(=O)C.C([BH3-])#N.[Na+].C([O-])(=O)C.[NH4+]>CO.CC(C)=O>[Cl:8][C:9]1[CH:10]=[CH:11][C:12]([NH:15][C:16](=[O:33])[C:17]2[CH:22]=[C:21]([I:23])[CH:20]=[CH:19][C:18]=2[NH:24][C:25]([CH:27]2[CH2:28][CH2:29][N:30]([CH:2]([CH3:3])[CH3:34])[CH2:31][CH2:32]2)=[O:26])=[N:13][CH:14]=1

참가 물질

7

실험 절차

To a stirring suspension of N-(5-chloropyridin-2-yl)-5-iodo-2-[(4-piperidinylcarbonyl)amino]benzamide trifluoroacetate (1.5 g, 2.52 mmol) in methanol (25 mL) was added acetone (25 mL), followed by acetic acid (0.6 mL, 10 mmol), and then sodium cyanoborohydride (0.67 g, 10 mmol). After stirring overnight, the solution was treated with saturated aqueous ammonium acetate solution, concentrated, and partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The organic phase was washed with brine, dried over magnesium sulfate, filtered, and concentrated. The crude product was purified by chromatography over silica gel, eluting with a step gradient of 5–15% 2 M solution of ammonia/methanol in dichloromethane. The chromatography product was slurried in diethyl ether and filtered to give 0.87 g (65%) of a white solid.

후처리

  1. concentrationconcentrated
  2. custompartitioned between dichloromethane and saturated aqueous sodium bicarbonate
  3. washThe organic phase was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product was purified by chromatography over silica gel
  8. washeluting with a step gradient of 5–15% 2 M solution of ammonia/methanol in dichloromethane
  9. filtrationfiltered

출처 및 근거

ORD 기록
ord-27e8004c40f7499d8a9094ba59ca6168
출처 데이터셋
uspto-grants-2006_10
특허 번호
US07129245B2

반응 노트

불러오는 중…