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Phosphorus oxychloride → (2-Chloro-3-methyl-3H-imidazo[4,5-c]pyridin-4-yl)-dipropylamine

HRID 2235567
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HRID 2235567 반응식
[CH2:1]([N:4]([CH2:16][CH2:17][CH3:18])[C:5]1[C:10]2[N:11]([CH3:15])[C:12](=O)[NH:13][C:9]=2[CH:8]=[CH:7][N:6]=1)[CH2:2][CH3:3].P(Cl)(Cl)([Cl:21])=O>>[Cl:21][C:12]1[N:11]([CH3:15])[C:10]2[C:5]([N:4]([CH2:16][CH2:17][CH3:18])[CH2:1][CH2:2][CH3:3])=[N:6][CH:7]=[CH:8][C:9]=2[N:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 685842814-Dipropylamino-3-methyl-1,3-dihydroimidazo[4,5-c]pyridin-2-one

생성물 1

HCID 68582019(2-Chloro-3-methyl-3H-imidazo[4,5-c]pyridin-4-yl)-dipropylamine

실험 절차

A solution of 0.91 g (3.66 mmol) of 4-dipropylamino-3-methyl-1,3-dihydroimidazo[4,5-c]pyridin-2-one in 30 mL of phosphorous oxychloride was heated at 100° C. overnight and concentrated in vacuo. The thus obtained residue was quenched with water, adjusted with aqueous sodium bicarbonate to pH 5, and extracted with ethyl acetate. The organics were dried over sodium sulfate, filtered and concentrated in vacuo. The thus obtained residue was triturated with acetonitrile, filtered, and the filtrate, which contained the desired product, was concentrated in vacuo. The residue thus obtained (0.18 g, 18%) was used in the next reaction without further purification.

후처리

  1. concentration
concentrated in vacuo
  • customThe thus obtained residue was quenched with water
  • extractionextracted with ethyl acetate
  • dry with materialThe organics were dried over sodium sulfate
  • filtrationfiltered
  • concentrationconcentrated in vacuo
  • customThe thus obtained residue was triturated with acetonitrile
  • filtrationfiltered
  • concentrationwas concentrated in vacuo
  • customThe residue thus obtained (0.18 g, 18%)
  • customwas used in the next reaction without further purification
  • 출처 및 근거

    ORD 기록
    ord-481ae704dc264cc5b158c3786b29df36
    출처 데이터셋
    uspto-grants-2010_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07714009B2

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