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

HRID 970592
ノート
印刷プレビュー

反応式

HRID 970592 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

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

生成物 1

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

実験手順

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).

後処理

  • 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
  • 出典と根拠

    ORDレコード
    ord-6980db59a21b4348a0232fe22564f017
    出典データセット
    uspto-grants-2007_12
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07312221B2

    反応ノート

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