Isatin → 3-Methyl-2-phenylquinoline-4-carboxylic acid
反応式
[NH:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4](=O)[C:2]1=[O:3].[C:12]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)(=O)[CH2:13][CH3:14].[OH-:22].[K+]>C(O)C.O>[CH3:14][C:13]1[C:12]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[N:1][C:11]2[C:6]([C:4]=1[C:2]([OH:22])=[O:3])=[CH:7][CH:8]=[CH:9][CH:10]=2参加物
実験手順
A solution of isatin (5.00 g, 34.0 mmol), propiophenone (5.47 g, 5.43 mL, 40.8 mmol), and potassium hydroxide pellets (6.73 g, 102 mmol) in ethanol (40 mL) was stirred at reflux for 23 h. After cooling, the solvent was removed in vacuo to give a brown residue. The residue was dissolved in water (75 mL) and washed with diethyl ether (4×100 mL). The aqueous layer was cooled by the addition of ice (˜50 g) and acidified to pH˜1 via dropwise addition of concentrated HCl with stirring. A solid precipitate was collected by filtration, washed with water and dried to provide the title compound as a yellowish-tan solid (7.59 g, 85%), which was used without further purification. MS (API+): M+1: 264 (45%), 220 (100); %); 1H NMR (300 MHz, DMSO-d6) d 2.39 (s, 3H), 7.49-7.57 (m, 3H), 7.59-7.72 (m, 7.76-7.84 (m, 2H), 8.06 (d, J=8.5 Hz, 1H), 14.20 (v br s, 1H, exchangeable).
後処理
- temperatureat reflux for 23 h
- temperatureAfter cooling
- customthe solvent was removed in vacuo
- customto give a brown residue
- washwashed with diethyl ether (4×100 mL)
- temperatureThe aqueous layer was cooled by the addition of ice (˜50 g)
- additionacidified to pH˜1 via dropwise addition of concentrated HCl
- filtrationA solid precipitate was collected by filtration
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-9961680a2fa6484eaec9794223c9a1cb
- 出典データセット
- uspto-grants-2005_06
- 特許番号
- US06906193B2
反応ノート
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