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Anisole → 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine

HRID 1783385
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HRID 1783385 반응식
O[C:2]1[N:3]=[CH:4][C:5]([O:11][CH3:12])=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2.C1(OC)C=CC=CC=1.P(Br)(Br)([Br:23])=O>>[Br:23][C:2]1[N:3]=[CH:4][C:5]([O:11][CH3:12])=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2
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참가 물질

4

반응물 3

HCID 7519AnisoleHCID 24613Phosphorus oxybromideHCID 178493790HCID 178493790, 화합물

생성물 1

HCID 207912447-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine수율 27.4%

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온도
160 °C

실험 절차

To a flask containing 7-hydroxy-4-methoxy-6-azaindole (0.200 g, 1.22 mmol) was added anisole (3 mL) and then POBr3 (1.57 g, 6.09 mmol). The system was purged with Ar and then it was heated at 160° C. (oil bath temperature) for 1 h. The reaction mixture was then allowed to cool to room temperature, quenched with 2M HBr (5 mL) and extracted with methyl t-butyl ether. The aqueous phase was separated and the pH was adjusted to 6-7, after which it was extracted with EtOAc. The resulting organic phase was dried (MgSO4) and evaporated to give a solid residue which was chromatographed (SiO2/5% MeOH-DCM) to afford the title compound (0.076 g, 27%) as a white solid:

후처리

  1. customThe system was purged with Ar
  2. temperatureto cool to room temperature
  3. customquenched with 2M HBr (5 mL)
  4. extractionextracted with methyl t-butyl ether
  5. customThe aqueous phase was separated
  6. extractionafter which it was extracted with EtOAc
  7. dry with materialThe resulting organic phase was dried (MgSO4)
  8. customevaporated
  9. customto give a solid residue which
  10. customwas chromatographed (SiO2/5% MeOH-DCM)

출처 및 근거

ORD 기록
ord-0c85563ae20744998fe7eb3cad8fa76e
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07501419B2

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