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

HRID 240997
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HRID 240997 반응식
[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
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참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

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+).

후처리

  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)

출처 및 근거

ORD 기록
ord-032ef48705184554a0eeedffe1217a7a
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08648066B2

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