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Phosphorus oxychloride → 4-chloro-1,3-dimethyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine

HRID 1764095
ノート
印刷プレビュー

反応式

HRID 1764095 の反応式
[CH3:1][N:2]1[C:6]2=[N:7][C:8]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[CH:9][C:10](O)=[C:5]2[C:4]([CH3:18])=[N:3]1.P(Cl)(Cl)([Cl:21])=O>>[Cl:21][C:10]1[CH:9]=[C:8]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[N:7]=[C:6]2[N:2]([CH3:1])[N:3]=[C:4]([CH3:18])[C:5]=12
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 178433989HCID 178433989、化合物

生成物 1

HCID 227705064-chloro-1,3-dimethyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine

実験手順

73 gms. of 1,3-dimethyl-4-hydroxy-6-phenyl-1H-pyrazolo[3,4-b]pyridine (0.31 mol.) are refluxed in 800 ml. of phosphorus oxychloride for 6 hours. The excess phosphorus oxychloride is removed in vacuo and the oily residue is treated with ice-water by which operation the compound becomes solid. The compound is extracted with ether, washed with an aqueous sodium carbonate solution (10%) and again with water. Evaporation of the dried (Na2SO4) and charcoal treated ethereal extract provides 4-chloro-1,3 -dimethyl-6-phenyl-1H-pyrazolo[3,4-b]-pyridine which is washed with absolute ethanol, yield: 55.6 gms. (69.8%) of white product melting at 89°-90° C.

後処理

  1. customThe excess phosphorus oxychloride is removed in vacuo
  2. additionthe oily residue is treated with ice-water by which operation the compound
  • extractionThe compound is extracted with ether
  • washwashed with an aqueous sodium carbonate solution (10%) and again with water
  • customEvaporation of the
  • dry with materialdried (Na2SO4) and charcoal treated ethereal
  • extractionextract
  • 出典と根拠

    ORDレコード
    ord-22cf88fcf58b4feb9eb58d6987952e55
    出典データセット
    uspto-grants-1978_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04115394

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