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Phosphorus oxychloride → 4-Chloro-6-fluoro-1-methyl-2-oxo-1,2-dihydroquinoline-3-carbonitrile

HRID 970507
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반응식

HRID 970507 반응식
C1([NH:7][C:8]([C:10]2[C:11](=[O:23])[N:12]([CH3:22])[C:13]3[C:18]([C:19]=2O)=[CH:17][C:16]([F:21])=[CH:15][CH:14]=3)=O)CCCCC1.P(Cl)(Cl)([Cl:26])=O>>[Cl:26][C:19]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([F:21])[CH:17]=2)[N:12]([CH3:22])[C:11](=[O:23])[C:10]=1[C:8]#[N:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 694755656-Fluoro 4-hydroxy-1-methyl-2-oxo-1,2-dihydro-quinoline-3-carboxylic acid cyclohexylamide

생성물 1

HCID 210819614-Chloro-6-fluoro-1-methyl-2-oxo-1,2-dihydroquinoline-3-carbonitrile수율 56%

실험 절차

A solution of Compound 44 (2 g, 6.28 mmol) in 20 ml neat phosphorus oxychloride was heated at 90° C. for 5 h. The solvent was evaporated under reduced pressure. The residue was suspended in ice water and neutralized by solid sodium bicarbonate. The solids formed were filtered, washed by water, and purified by flash chromatography eluting with 1% methanol in dichloromethane to yield 0.80 g (56%) of yellow solids. M.P. 258° C. 1H NMR (DMSO-d6): δ 3.67 (s, 3H), 7.78-7.89 (m, 3H). EIMS m/z 259 (M+23).

후처리

  • customThe solvent was evaporated under reduced pressure
  • customThe solids formed
  • filtrationwere filtered
  • washwashed by water
  • custompurified by flash chromatography
  • washeluting with 1% methanol in dichloromethane
  • 출처 및 근거

    ORD 기록
    ord-e9edc79c4bf64d9fa74d933f34b65524
    출처 데이터셋
    uspto-grants-2007_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07312220B2

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