反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2[O:15][C:16]1[CH:22]=[CH:21][C:19]([NH2:20])=[C:18]([N+:23]([O-:25])=[O:24])[CH:17]=1.C(N(CC)CC)C.ClC(Cl)(O[C:37](=[O:43])OC(Cl)(Cl)Cl)Cl.[CH:45]([N:48]([CH:52]([CH3:54])[CH3:53])[CH2:49][CH2:50][NH2:51])([CH3:47])[CH3:46]>C(Cl)(Cl)Cl.O>[CH:45]([N:48]([CH:52]([CH3:54])[CH3:53])[CH2:49][CH2:50][NH:51][C:37]([NH:20][C:19]1[CH:21]=[CH:22][C:16]([O:15][C:6]2[C:5]3[C:10](=[CH:11][C:12]([O:13][CH3:14])=[C:3]([O:2][CH3:1])[CH:4]=3)[N:9]=[CH:8][CH:7]=2)=[CH:17][C:18]=1[N+:23]([O-:25])=[O:24])=[O:43])([CH3:47])[CH3:46]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitroaniline (100 mg) was dissolved in chloroform (10 ml) and triethylamine (1 ml) to prepare a solution. A solution of triphosgene (131 mg) in chloroform was then added to the solution, and the mixture was stirred at room temperature for 10 min. Next, N1,N1-diisopropyl-1,2-ethanediamine (63 mg) was added thereto, and the mixture was further stirred at room temperature for one hr. Water was added to stop the reaction, and the reaction solution was then extracted with chloroform, followed by concentration. The residue was purified on a column using chloroform/methanol to give the title compound (103 mg, yield 70%).
後処理
- stirringthe mixture was further stirred at room temperature for one hr
- customthe reaction
- extractionthe reaction solution was then extracted with chloroform
- concentrationfollowed by concentration
- customThe residue was purified on a column
出典と根拠
- ORDレコード
- ord-2ed5e4946b954909a33a62e6cee1d9b7
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07135466B2
関連ノート
読み込み中…