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Phosphorus oxychloride → 4-Chloro-1H-pyrazolo[3,4-b]pyridine

HRID 1861125
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HRID 1861125 반응식
[NH:1]1[C:5]2[NH:6][CH:7]=[CH:8][C:9](=O)[C:4]=2[CH:3]=[N:2]1.O=P(Cl)(Cl)[Cl:13]>>[Cl:13][C:9]1[CH:8]=[CH:7][N:6]=[C:5]2[NH:1][N:2]=[CH:3][C:4]=12
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참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 1357416021H-pyrazolo[3,4-b]pyridin-4-ol

생성물 1

HCID 3100454-Chloro-1H-pyrazolo[3,4-b]pyridine수율 60%

실험 절차

1,7-Dihydro-pyrazolo[3,4-b]pyridin4-one (1.2 g, 8.8 mmol) (Dorn, H. et al., Prakt. Chem., 324, 557-62 (1982)) in POCl3 (15 ml) at 0° C. was treated with PCd5 (2.5 mg, 0.01 mmol). The solution was allowed to warm to rt over 1 h, then heated to 90° C. and held 3h. The solution was concentrated under reduced pressure, then treated with ice and water (50 ml). The resulting mixture was extracted with ethyl acetate (100 ml), and the organic layer was washed with a saturated aqueous solution of sodium bicarbonate (30 ml). The organic layer was dried over MgSO4, then evaporated under reduced pressure to give 4-chloro-1H-pyrazolo[3,4-b]pyridine as a yellow solid (820 mg, 60%). 1H NMR (300 MHz, CDCl3) δ 8.57 (d, 1H, J=5.2 Hz), 8.25 (s, 1H), 7.28 (d, 1H, J=5.2 Hz).

후처리

  1. temperature
heated to 90° C.
  • concentrationThe solution was concentrated under reduced pressure
  • additiontreated with ice and water (50 ml)
  • extractionThe resulting mixture was extracted with ethyl acetate (100 ml)
  • washthe organic layer was washed with a saturated aqueous solution of sodium bicarbonate (30 ml)
  • dry with materialThe organic layer was dried over MgSO4
  • customevaporated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-c7861cf32f8c430d84b4a51baaf34537
    출처 데이터셋
    uspto-grants-2003_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06531491B1

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