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Phosphorus oxychloride → 4-(4-Chloro-5-pyrimidinyl)-o-phenylene diacetate

HRID 1755858
ノート
印刷プレビュー

反応式

HRID 1755858 の反応式
[C:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[C:12](=O)[NH:13][CH:14]=[N:15][CH:16]=2)=[CH:7][C:6]=1[O:18][C:19](=[O:21])[CH3:20])(=[O:3])[CH3:2].P(Cl)(Cl)([Cl:24])=O>>[C:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[C:12]([Cl:24])=[N:13][CH:14]=[N:15][CH:16]=2)=[CH:7][C:6]=1[O:18][C:19](=[O:21])[CH3:20])(=[O:3])[CH3:2]
参加物反応条件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 218053924-(3,4-Dihydro-4-oxo-5-pyrimidinyl)-o-phenylene diacetate

生成物 1

HCID 218054064-(4-Chloro-5-pyrimidinyl)-o-phenylene diacetate

反応条件

温度
100 °C

実験手順

4-(3,4-Dihydro-4-oxo-5-pyrimidinyl)-o-phenylene diacetate (194 mg) (0.67 mmol) are added to 5 ml of phosphorus oxychloride. After stirring at 100° C. for 6 hours the mixture is concentrated in a vacuum at 40° C. The residue is dissolved in dichloromethane/methanol (99:1 v/v) and the solution is washed with water. The solution is dried over sodium sulphate and concentrated. The residue is crystallized using ethanol. The beige crystals are filtered off under suction, washed with petroleum ether and dried in a high vacuum at room temperature. There are obtained 90 mg of 4-(4-chloro-5-pyrimidinyl)-o-phenylene diacetate of m.p. 108° C.

後処理

  1. concentrationis concentrated in a vacuum at 40° C
  2. dissolutionThe residue is dissolved in dichloromethane/methanol (99:1 v/v)
  3. washthe solution is washed with water
  4. dry with materialThe solution is dried over sodium sulphate
  5. concentrationconcentrated
  6. customThe residue is crystallized
  7. filtrationThe beige crystals are filtered off under suction
  8. washwashed with petroleum ether
  9. customdried in a high vacuum at room temperature

出典と根拠

ORDレコード
ord-b421f8e7a7f44dcdb012d8e53b99d51e
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05438052

反応ノート

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