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Phosphorus oxychloride → 2-Chloro-5-methoxy-3-methylquinazolin-4(3H)-one

HRID 598072
ノート
印刷プレビュー

反応式

HRID 598072 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[C:5](=[O:15])[N:6]([CH3:14])[C:7](=O)[NH:8]2.C(N(CC)C(C)C)(C)C.P(Cl)(Cl)([Cl:27])=O>>[Cl:27][C:7]1[N:6]([CH3:14])[C:5](=[O:15])[C:4]2[C:9](=[CH:10][CH:11]=[CH:12][C:3]=2[O:2][CH3:1])[N:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 24813Phosphorus oxychlorideHCID 81531DiisopropylethylamineHCID 672670575-methoxy-3-methyl-1H-quinazoline-2,4-dione

生成物 1

HCID 672666982-Chloro-5-methoxy-3-methylquinazolin-4(3H)-one収率 99.6%

実験手順

A mixture of 5-methoxy-3-methyl-1H-quinazoline-2,4-dione (165 mg, 0.800 mmol) and N,N-diisopropylethylamine (0.307 ml, 1.76 mmol) in phosphorus oxychloride (2.2 ml, 24.0 mmol) was refluxed for 18 h with stirring and concentrated to dryness under vacuum. The residue was diluted with water. The aqueous solution was extracted with dichloromethane. The extract was washed with water, dried over magnesium sulfate and concentrated under vacuum to afford 179 mg (99%) of the title compound. The residue was used for the next reaction without further purification.

後処理

  1. temperaturewas refluxed for 18 h
  2. concentrationconcentrated to dryness under vacuum
  3. additionThe residue was diluted with water
  4. extractionThe aqueous solution was extracted with dichloromethane
  5. washThe extract was washed with water
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-f689a00b142e4eb1b1f347283c07613c
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07897607B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート