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Phosphorus oxychloride → 4-Chloro-6,6-dimethyl-5,6,7,8-tetrahydroquinazoline

HRID 240997
ノート
印刷プレビュー

反応式

HRID 240997 の反応式
[CH3:1][C:2]1([CH3:13])[CH2:11][CH2:10][C:9]2[N:8]=[CH:7][NH:6][C:5](=O)[C:4]=2[CH2:3]1.P(Cl)(Cl)([Cl:16])=O>C(Cl)(Cl)Cl>[Cl:16][C:5]1[C:4]2[CH2:3][C:2]([CH3:13])([CH3:1])[CH2:11][CH2:10][C:9]=2[N:8]=[CH:7][N:6]=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 2

HCID 24813Phosphorus oxychlorideHCID 1357423376,6-Dimethyl-3,4,5,6,7,8-hexahydroquinazolin-4-one

生成物 1

HCID 866478114-Chloro-6,6-dimethyl-5,6,7,8-tetrahydroquinazoline収率 75%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

To 6,6-dimethyl-5,6,7,8-tetrahydroquinazolin-4(3H)-one (6.41 g, 36 mmol) in chloroform (10 mL) added phosphorus oxychloride (10 mL) and refluxed for 2 hours. The mixture was concentrated to an oil, then diluted with ethyl acetate (80 mL) and washed with saturated sodium carbonate (50 mL) and brine (25 mL). The solution was dried over anhydrous sodium sulfate, filtered and concentrated, then the residue purified by silica gel column chromatography (ethyl acetate/hexanes, 1:8) to give 4-chloro-6,6-dimethyl-5,6,7,8-tetrahydroquinazoline (5.3 g, 75% yield) as a yellow solid. 1H NMR (400 MHz, CDCl3): 8.72 (s, 1H), 2.52 (t, 2H), 2.14 (s, 2H), 1.48 (t 2H), 0.93 (s, 6H); MS (EI) for C10H13ClN2: 197 (MH+).

後処理

  1. temperaturerefluxed for 2 hours
  2. concentrationThe mixture was concentrated to an oil
  3. additiondiluted with ethyl acetate (80 mL)
  4. washwashed with saturated sodium carbonate (50 mL) and brine (25 mL)
  5. dry with materialThe solution was dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customthe residue purified by silica gel column chromatography (ethyl acetate/hexanes, 1:8)

出典と根拠

ORDレコード
ord-032ef48705184554a0eeedffe1217a7a
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08648066B2

反応ノート

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