Triethylamine → N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamide

HRID 38246

반응식

HRID 38246 반응식
Cl.[N:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](Cl)=[O:9].CCN(CC)CC.[CH3:18][O:19][C:20]1[CH:21]=[C:22]([CH:24]=[CH:25][C:26]=1[O:27][C:28]1[N:33]=[CH:32][CH:31]=[CH:30][N:29]=1)[NH2:23]>C(Cl)Cl>[CH3:18][O:19][C:20]1[CH:21]=[C:22]([NH:23][C:8](=[O:9])[C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][N:2]=2)[CH:24]=[CH:25][C:26]=1[O:27][C:28]1[N:29]=[CH:30][CH:31]=[CH:32][N:33]=1

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 135033Picolinoyl Chloride HydrochlorideHCID 621109613-Methoxy-4-(pyrimidin-2-yloxy)aniline

생성물 1

HCID 42645238N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamide수율 19.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

According to Scheme 3 Step 3: Picolinoyl chloride hydrochloride (1.33 mmol, 256 mg) and Et3N (2.67 mmol, 0.37 mL) were added sequentially to a solution of 3-methoxy-4-(pyrimidin-2-yloxy)aniline (0.89 mmol, 193 mg) in DCM (3 mL) at 0° C. The reaction mixture was stirred at room temperature for 2 hours. The organic phase was washed with a saturated solution of NaHCO3. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over MgSO4, was filtered and was concentrated under reduced pressure. The crude product was purified by flash chromatography over C18 column using water/ACN (70:30) as eluent to afford N-(3-methoxy-4-(pyrimidin-2-yloxy)phenyl)picolinamide (0.17 mmol, 55 mg, 19%) as a white solid.

후처리

  1. washThe organic phase was washed with a saturated solution of NaHCO3
  2. extractionThe aqueous phase was extracted with AcOEt
  3. washThe organic phase was washed with brine
  4. dry with materialwas dried over MgSO4
  5. filtrationwas filtered
  6. concentrationwas concentrated under reduced pressure
  7. customThe crude product was purified by flash chromatography over C18 column

출처 및 근거

ORD 기록
ord-a7f5fcf130d348a486c01d6789d738a7
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08524726B2

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