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Phosphorus oxychloride → 4-Chloro-7-isopropylquinazoline

HRID 884003
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HRID 884003 반응식
[CH:1]([C:4]1[CH:13]=[C:12]2[C:7]([C:8](=O)[NH:9][CH:10]=[N:11]2)=[CH:6][CH:5]=1)([CH3:3])[CH3:2].P(Cl)(Cl)([Cl:17])=O>>[Cl:17][C:8]1[C:7]2[C:12](=[CH:13][C:4]([CH:1]([CH3:3])[CH3:2])=[CH:5][CH:6]=2)[N:11]=[CH:10][N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 1361233184-Hydroxy-7-isopropylquinazoline

생성물 1

HCID 866155654-Chloro-7-isopropylquinazoline수율 97%

실험 절차

The product of Example 91E (100 mg, 0.5313 mmol) in phosphorous oxychloride (2 mL) was heated under a nitrogen atmosphere at reflux for one hour. The reaction was cooled and concentrated by rotary evaporation. The residue was dissolved in ethyl acetate (50 mL) and washed sequentially with saturated aqueous sodium hydrogencarbonate (2×25 mL), water (25 mL), and brine (25 mL). The organic extract was dried over sodium sulfate, filtered, and concentrated by rotary evaporation to afford the title compound as a yellow oil (107 mg, 0.5177 mmol, 97%). 1H NMR (300 MHz, DMSO-D6) δ ppm 1.33 (d, J=6.99 Hz, 6 H) 3.14-3.29 (m, 1 H) 7.86 (dd, J=8.64, 1.65 Hz, 1 H) 7.93 (s, 1 H) 8.22 (d, J=8.46 Hz, 1 H) 9.07 (s, 1 H).

후처리

  1. temperatureat reflux for one hour
  • temperatureThe reaction was cooled
  • concentrationconcentrated by rotary evaporation
  • dissolutionThe residue was dissolved in ethyl acetate (50 mL)
  • washwashed sequentially with saturated aqueous sodium hydrogencarbonate (2×25 mL), water (25 mL), and brine (25 mL)
  • extractionThe organic extract
  • dry with materialwas dried over sodium sulfate
  • filtrationfiltered
  • concentrationconcentrated by rotary evaporation
  • 출처 및 근거

    ORD 기록
    ord-44dda497ebf14870bee03c5d074352b6
    출처 데이터셋
    uspto-grants-2012_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08236950B2

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