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Phosphorus oxychloride → 4-Chloro-2-chloromethyl-7-(3-trifluoromethyl-pyridin-2-yl)-quinazoline

HRID 2113612
ノート
印刷プレビュー

反応式

HRID 2113612 の反応式
[Cl:1][CH2:2][C:3]1[NH:12][C:11](=O)[C:10]2[C:5](=[CH:6][C:7]([C:14]3[C:19]([C:20]([F:23])([F:22])[F:21])=[CH:18][CH:17]=[CH:16][N:15]=3)=[CH:8][CH:9]=2)[N:4]=1.O=P(Cl)(Cl)[Cl:26]>>[Cl:26][C:11]1[C:10]2[C:5](=[CH:6][C:7]([C:14]3[C:19]([C:20]([F:23])([F:22])[F:21])=[CH:18][CH:17]=[CH:16][N:15]=3)=[CH:8][CH:9]=2)[N:4]=[C:3]([CH2:2][Cl:1])[N:12]=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 1356820662-chloromethyl-7-(3-trifluoromethyl-pyridin-2-yl)-3H-quinazolin-4-one

生成物 1

HCID 220301504-Chloro-2-chloromethyl-7-(3-trifluoromethyl-pyridin-2-yl)-quinazoline

実験手順

Reflux a mixture of 2-chloromethyl-7-(3-trifluoromethyl-pyridin-2-yl)-3H-quinazolin-4-one and POCl3 for 16 hours. Cool the mixture and concentrate under reduced pressure. Partition the residue between EtOAc and saturated NaHCO3 solution. Wash the EtOAc portion with additional NaHCO3 and then dry (Na2SO4) and concentrate under reduced pressure. Filter the brown residue through 2 inches of silica gel (1:1 EtOAc/hexanes eluent) and concentrate under reduced pressure to give 4-chloro-2-chloromethyl-7-(3-trifluoromethyl-pyridin-2-yl)-quinazoline.

後処理

  1. temperatureReflux
  2. temperature
Cool the mixture
  • concentrationconcentrate under reduced pressure
  • customPartition the residue between EtOAc and saturated NaHCO3 solution
  • washWash the EtOAc portion with additional NaHCO3
  • dry with materialdry (Na2SO4)
  • concentrationconcentrate under reduced pressure
  • filtrationFilter the brown residue through 2 inches of silica gel (1:1 EtOAc/hexanes eluent)
  • concentrationconcentrate under reduced pressure
  • 出典と根拠

    ORDレコード
    ord-09b40d1231ba47b19d91f2fb61965382
    出典データセット
    uspto-grants-2008_10
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07432275B2

    反応ノート

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