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Phosphorus oxychloride → 4-Chlorobenzo[g]quinoline-3-carbonitrile

HRID 989287
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HRID 989287 반응식
O=[C:2]1[C:11]2[C:6](=[CH:7][C:8]3[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=3[CH:10]=2)[NH:5][CH:4]=[C:3]1[C:16]#[N:17].P(Cl)(Cl)([Cl:20])=O>CN(C)C=O>[Cl:20][C:2]1[C:11]2[C:6](=[CH:7][C:8]3[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=3[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]#[N:17]
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 98344134-Oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile

생성물 1

HCID 98346304-Chlorobenzo[g]quinoline-3-carbonitrile수율 49.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide촉매

반응 조건

온도
105 °C

실험 절차

A reaction mixture of 3.5 g (16 mmol) of 4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile in 35 mL of phosphorus oxychloride and 22 drops of N,N-dimethylformamide (DMF) is heated at 100-110° C. for 5 hours. After cooling, the mixture is concentrated to dryness in vacuo to give a dark residue. The residue is partitioned between methylene chloride and ice-cooled saturated aqueous sodium carbonate solution. The organic layer is washed with ice-cooled brine and dried over sodium sulfate. The organic solvent is passed through a short column of silica gel, and further eluted with additional methylene chloride. Removal of the solvent yields 1.89 g (49.5%) of the product as a bright yellow solid, mp 253-255° C.

후처리

  1. temperatureAfter cooling
  2. concentrationthe mixture is concentrated to dryness in vacuo
  3. customto give a dark residue
  4. customThe residue is partitioned between methylene chloride and ice-
  5. temperaturecooled saturated aqueous sodium carbonate solution
  6. washThe organic layer is washed with ice-
  7. temperaturecooled brine
  8. dry with materialdried over sodium sulfate
  9. washfurther eluted with additional methylene chloride
  10. customRemoval of the solvent

출처 및 근거

ORD 기록
ord-0efc204b03744a3faba6d880bb8c472b
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06638929B2

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