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Phosphorus oxychloride → 4-((4-Chloropyrimidin-2-yl)amino)benzonitrile

HRID 716610
ノート
印刷プレビュー

反応式

HRID 716610 の反応式
O=[C:2]1[CH:7]=[CH:6][NH:5][C:4]([NH:8][C:9]2[CH:16]=[CH:15][C:12]([C:13]#[N:14])=[CH:11][CH:10]=2)=[N:3]1.O=P(Cl)(Cl)[Cl:19]>>[Cl:19][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH:8][C:9]2[CH:16]=[CH:15][C:12]([C:13]#[N:14])=[CH:11][CH:10]=2)[N:3]=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 178510039HCID 178510039、化合物

生成物 1

HCID 111955954-((4-Chloropyrimidin-2-yl)amino)benzonitrile

実験手順

A mixture of 4-[(1,4-dihydro-4-oxo-2-pyrimidinyl)amino]benzonitrile (0.12 mol) in POCl3 (90 ml) was stirred and refluxed under Argon for 20 minutes. The reaction mixture was slowly poured onto 750 ml ice/water, and the solid was separated by filtration. The solid was suspended in 500 ml water, and the pH of the suspension was adjusted to neutral by adding a 20% NaOH solution. The solid was again separated by filtration, suspended in 200 ml 2-propanone, and 1000 ml CH2Cl2 was added. The mixture was heated until all solid had dissolved. After cooling to room temperature, the aqueous layer was separated, and the organic layer was dried. During removal of the drying agent by filtration, a white solid formed in the filtrate. Further cooling of the filtrate in the freezer, followed by filtration, yielded 21.38 g (77.2%) of [4-[(4-chloro-2-pyrimidinyl)amino]benzonitrile (interm. 5).

後処理

temperature
refluxed under Argon for 20 minutes
  • customthe solid was separated by filtration
  • additionby adding a 20% NaOH solution
  • customThe solid was again separated by filtration
  • addition1000 ml CH2Cl2 was added
  • temperatureThe mixture was heated until all solid
  • dissolutionhad dissolved
  • customthe aqueous layer was separated
  • customthe organic layer was dried
  • customDuring removal of the drying agent
  • filtrationby filtration
  • customa white solid formed in the filtrate
  • temperatureFurther cooling of the filtrate in the freezer
  • filtrationfollowed by filtration
  • 出典と根拠

    ORDレコード
    ord-cf7e96e3e8054e0e9929f54daad69d78
    出典データセット
    uspto-grants-2015_11
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US09192577B2

    反応ノート

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