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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 7-Fluoroquinolin-2(1H)-one

HRID 969310
ノート
印刷プレビュー

反応式

HRID 969310 の反応式
C(C1C(=O)C(Cl)=C(Cl)C(=O)C=1C#N)#N.[F:15][C:16]1[CH:25]=[C:24]2[C:19]([CH2:20][CH2:21][C:22](=[O:26])[NH:23]2)=[CH:18][CH:17]=1>O1CCOCC1>[F:15][C:16]1[CH:25]=[C:24]2[C:19]([CH:20]=[CH:21][C:22](=[O:26])[NH:23]2)=[CH:18][CH:17]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 138300Carbostyril, 3,4-dihydro-7-fluoro-

生成物 1

HCID 190675757-Fluoroquinolin-2(1H)-one収率 18.9%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

DDQ (0.42 g, 1.9 mmol) was added to a solution of 7-fluoro-3,4-dihydro-1H-quinolin-2-one (0.20 g 1.2 mmol) in dioxane (25 mL) and the resulting mixture was refluxed under an Argon atmosphere for 16 h. The mixture was concentrated under reduced pressure and sat aqueous Na2CO3 solution (25 mL) was added, and this was extracted with an organic mixture (MeOH/CH2Cl2 1:10, 3×50 mL). The combined organic phase was dried (Na2SO4), filtered, concentrated under reduced pressure and purified by combi flash LC (SiO2; CH2Cl2/MeOH 10:1) to give the title compound (0.037 g, 18%). 1H NMR (DMSO-D6) δ 11.8 (s, 1H), 7.88 (d, J=9.6 Hz, 1H), 7.74-7.65 (m, 1H), 7.05-6.95 (m, 2H), 6.43, (d, J=9.6 Hz); 13C NMR (CDMSO-D6) δ 163.0 (d, J=247 Hz), 161.9, 140.4 (d, J=13 Hz), 130.4 (d, J=11 Hz), 120.9, 116.1, 109.8 (d, J=23), 101.0 (d, J=25 Hz).

後処理

  1. temperaturethe resulting mixture was refluxed under an Argon atmosphere for 16 h
  2. concentrationThe mixture was concentrated under reduced pressure
  3. additionwas added
  4. extractionthis was extracted with an organic mixture (MeOH/CH2Cl2 1:10, 3×50 mL)
  5. dry with materialThe combined organic phase was dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. custompurified by combi flash LC (SiO2; CH2Cl2/MeOH 10:1)

出典と根拠

ORDレコード
ord-f312168461c9433fae9b947d34d25d3b
出典データセット
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07307075B2

反応ノート

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