HCID 21654345、化合物 → HCID 19982481、化合物
反応式
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:21]=[C:20]([C:22]([OH:24])=O)[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[N:13]=2)=[CH:8][C:7]=1[O:25][CH3:26])[CH2:2][CH2:3][CH3:4]>S(Cl)(Cl)=O>[CH2:20]([CH:19]([CH2:18][CH2:17][CH2:16][CH3:15])[CH2:14][NH:13][C:22]([C:20]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=[C:12]([C:9]2[CH:10]=[CH:11][C:6]([O:5][CH2:1][CH2:2][CH2:3][CH3:4])=[C:7]([O:25][CH3:26])[CH:8]=2)[CH:21]=1)=[O:24])[CH3:21]参加物
反応条件
- 温度
- 80 °C
実験手順
10.5 g of 2-(4'-butyoxy-3'-methoxyphenyl)quinoline-4-carboxylic acid (prepared as described in Example 7) were dissolved in 50 g of thionyl chloride, and the solution was refluxed for half an hour. The excess thionyl chloride was distilled off under reduced pressure, and the residue was introduced into 50 g of 2-ethylhexylamine with ice-water cooling. The mixture was stirred at 25° C. for 1 hour and at 80° C. for a further half hour. After cooling, 200 ml of methanol were added to dilute the mixture, and the precipitated product was washed with methanol and water and dried at 60° C. in a drying cabinet. 6.5 g were obtained of N-(2'-ethylhexyl)-2-(4'-butoxy-3'-methoxyphenyl)quinoline-4-carboxamide. The colorless crystals melt at 118° C. and have a λmax in toluene at 352 nm. In 2% strength methanolic hydrochloric acid the λmax is 403 nm.
後処理
- temperaturethe solution was refluxed for half an hour
- distillationThe excess thionyl chloride was distilled off under reduced pressure
- additionthe residue was introduced into 50 g of 2-ethylhexylamine with ice-water cooling
- temperatureAfter cooling
- addition200 ml of methanol were added
- additionto dilute the mixture
- washthe precipitated product was washed with methanol and water
- customdried at 60° C. in a drying cabinet
出典と根拠
- ORDレコード
- ord-e403abb66dc5495ba3df15f57065ab76
- 出典データセット
- uspto-grants-1991_12
- 特許番号
- US05071987
反応ノート
読み込み中…