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

HRID 2181561
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HRID 2181561 반응식
[NH:1]1[C:5]2[NH:6][CH:7]=[CH:8][C:9](=O)[C:4]=2[CH:3]=[N:2]1.P(Cl)(Cl)(Cl)(Cl)[Cl:12]>O=P(Cl)(Cl)Cl>[Cl:12][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

4

반응물 2

HCID 24819Phosphorus pentachlorideHCID 1357416021H-pyrazolo[3,4-b]pyridin-4-ol

생성물 1

HCID 3100454-Chloro-1H-pyrazolo[3,4-b]pyridine수율 53,396.199%

시약·촉매·용매 1

HCID 24813Phosphorus oxychloride용매

실험 절차

1,7-Dihydro-pyrazolo[3,4-b]pyridin-4-one (1.2 g, 8.8 mmol) (Dorn, H. et al., Prakt. Chem., 324, 55762 (1982)) in POCl3 (15 ml) at 0° C. was treated with PCl5 (2.5 mg, 0.01 mmol). The solution was allowed to warm to rt over 1 h, then heated to 90° C. and held 3 h. 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 857 (d, 1H, J=5.2 Hz), 8.25 (s, 1H), 7.28 (d, 1H, J=5.2 Hz).

후처리

  1. temperatureheated to 90° C.
  2. concentrationThe solution was-concentrated under reduced pressure
  3. additiontreated with ice and water (50 ml)
  4. extractionThe resulting mixture was extracted with ethyl acetate (100 ml)
  5. washthe organic layer was washed with a saturated aqueous solution of sodium bicarbonate (30 ml)
  6. dry with materialThe organic layer was dried over MgSO4
  7. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-cedc3abbcbef4591a6f39ebd2998a67b
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06891044B2

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