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Phosphorus oxychloride → HCID 59574224、化合物

HRID 2092040
ノート
印刷プレビュー

反応式

HRID 2092040 の反応式
O=[C:2]1[C:7]([CH2:8][N:9]2[C:17](=[O:18])[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10]2=[O:19])=[CH:6][CH:5]=[N:4][NH:3]1.P(Cl)(Cl)([Cl:22])=O>>[Cl:22][C:2]1[N:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH2:8][N:9]1[C:17](=[O:18])[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]1=[O:19]
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 oxychloride2 回HCID 595748042-[(3-Oxo-2,3-dihydropyridazin-4-yl)methyl]isoindoline-1,3-dione

生成物 1

HCID 59574224HCID 59574224、化合物収率 89%

実験手順

2-[(3-Oxo-2,3-dihydropyridazin-4-yl)methyl]-1H-isoindole-1,3(2H)-dione (1.1 g, 4.27 mmol) was mixed with phosphoryl chloride (10 mL) and heated to reflux for 1 hour. After completion of the reaction, phosphoryl chloride was removed under reduced pressure. The resulting residue was diluted with chloroform and water. The organic layer was separated, dried over anhydrous magnesium sulfate, and the solvent was removed by vacuum distillation. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1) to give the desired product (89% yield).

後処理

  1. temperatureheated
  2. temperature
to reflux for 1 hour
  • customwas removed under reduced pressure
  • additionThe resulting residue was diluted with chloroform and water
  • customThe organic layer was separated
  • dry with materialdried over anhydrous magnesium sulfate
  • customthe solvent was removed by vacuum distillation
  • customThe resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=9/1)
  • 出典と根拠

    ORDレコード
    ord-cab618e620a041d9b7dba1373d9ae338
    出典データセット
    uspto-grants-2013_05
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08440666B2

    反応ノート

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