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

HRID 2235567
ノート
印刷プレビュー

反応式

HRID 2235567 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

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

生成物 1

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

実験手順

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.

後処理

  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
  • 出典と根拠

    ORDレコード
    ord-481ae704dc264cc5b158c3786b29df36
    出典データセット
    uspto-grants-2010_05
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07714009B2

    反応ノート

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