Potassium Hydroxide → Brequinar Analog

HRID 2118652ノート

反応式

HRID 2118652 の反応式
[CH3:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:7][CH:6]=1)=O.[F:17][C:18]1[CH:19]=[C:20]2[C:24](=[CH:25][CH:26]=1)[NH:23][C:22](=[O:27])[C:21]2=O.[OH-:29].[K+]>C(O)C.O>[C:8]1([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:7]=[CH:6][C:5]([C:3]2[C:2]([CH3:1])=[C:21]([C:22]([OH:27])=[O:29])[C:20]3[C:24](=[CH:25][CH:26]=[C:18]([F:17])[CH:19]=3)[N:23]=2)=[CH:10][CH:9]=1

参加物

6

実験手順

4-Phenylpropiophenone (18.9 g, 0.09 mole) and 5-fluoroisatin (20 g, 0.09 mole) were suspended in 360 ml of ethanol and stirred mechanically as a solution of 35.2 g KOH in 100 ml water was added dropwise over 15 minutes. The reaction mixture was heated at reflux for 12 hours, cooled, and the ethanol evaporated under reduced pressure. The resulting yellow solid was dissolved in water and washed with ethyl ether. The aqueous layer was cooled to 5° and acidified with glacial acetic acid. The resulting yellow precipitate was filtered and dried. Recrystallization from 200 ml of dimethylformamide and 25 ml water provided 13.8 g of 2-(4-biphenylyl)-6-fluoro-3-methylquinoline-4-carboxylic acid as a white solid, m.p. 303°-306°(d).

後処理

  1. additionwas added dropwise over 15 minutes
  2. temperatureThe reaction mixture was heated
  3. temperatureat reflux for 12 hours
  4. temperaturecooled
  5. customthe ethanol evaporated under reduced pressure
  6. dissolutionThe resulting yellow solid was dissolved in water
  7. washwashed with ethyl ether
  8. temperatureThe aqueous layer was cooled to 5°
  9. filtrationThe resulting yellow precipitate was filtered
  10. customdried
  11. customRecrystallization from 200 ml of dimethylformamide and 25 ml water

出典と根拠

ORDレコード
ord-64f51a43b2a44630980313546e7e05d1
出典データセット
uspto-grants-1987_07
特許番号
US04680299

反応ノート

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