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

HRID 1783385
ノート
印刷プレビュー

反応式

HRID 1783385 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 7519AnisoleHCID 24613Phosphorus oxybromideHCID 178493790HCID 178493790、化合物

生成物 1

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

反応条件

温度
160 °C

実験手順

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:

後処理

  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)

出典と根拠

ORDレコード
ord-0c85563ae20744998fe7eb3cad8fa76e
出典データセット
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07501419B2

反応ノート

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