Ethanol → 1-Cyclopropyl-3-ethoxycarbonyl-7,8,9-trifluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine
反応式
[CH:1]1([NH2:4])[CH2:3][CH2:2]1.Cl[C:6]1[C:15]([C:16]([C:18](=[CH:24]N(C)C)[C:19]([O:21][CH2:22][CH3:23])=[O:20])=[O:17])=[CH:14][C:13]2[C:8](=[C:9]([F:30])[C:10]([F:29])=[C:11]([F:28])[CH:12]=2)[N:7]=1.C(O)C.C1CCN2C(=NCCC2)CC1>ClC(Cl)Cl>[CH:1]1([N:4]2[C:6]3[N:7]=[C:8]4[C:9]([F:30])=[C:10]([F:29])[C:11]([F:28])=[CH:12][C:13]4=[CH:14][C:15]=3[C:16](=[O:17])[C:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:24]2)[CH2:3][CH2:2]1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 80 °C
実験手順
Cyclopropylamine (4.12 g) is added in the course of 5 minutes to a solution, maintained at a temperature in the region of 20° C., of ethyl 2-(2-chloro-6,7,8-trifluoro-3-quinolinecarbonyl)-3-(dimethylamino)acrylate (7 g) in trichloromethane (100 cc), and the mixture is stirred for a further 4 hours at the same temperature. The reaction mixture is concentrated under reduced pressure (20 kPa) at approximately 50° C. The oily residue obtained is taken up with ethanol (100 cc) and DBU (3 g). The mixture is heated to 80° C. and kept stirring at the same temperature for 1 hour and a half. After cooling to approximately 20° C., the insoluble matter is drained and washed with ethanol (2×30 cc) and isopropyl ether (2×30 cc). 1-Cyclopropyl-3-ethoxycarbonyl-7,8,9-trifluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine (4.5 g) is obtained in the form of a colorless solid, m.p. 260° C.
後処理
- concentrationThe reaction mixture is concentrated under reduced pressure (20 kPa) at approximately 50° C
- customThe oily residue obtained
- stirringkept stirring at the same temperature for 1 hour
- temperatureAfter cooling to approximately 20° C.
- washwashed with ethanol (2×30 cc) and isopropyl ether (2×30 cc)
出典と根拠
- ORDレコード
- ord-aa9c30ce7d314705b014427735207341
- 出典データセット
- uspto-grants-1991_10
- 特許番号
- US05053509
反応ノート
読み込み中…