1,1-Dichloroethane → 2-(cyclohexylamino)-6-fluoro-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)nicotinamide
反応式
CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.ClC(Cl)C.[CH:29]1([NH:35][C:36]2[N:44]=[C:43]([F:45])[CH:42]=[CH:41][C:37]=2[C:38]([OH:40])=O)[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1.[NH2:46][C:47]1[CH:56]=[C:55]2[C:50]([CH2:51][CH2:52][C:53](=[O:58])[N:54]2[CH3:57])=[CH:49][CH:48]=1>C(N(CC)CC)C>[CH:29]1([NH:35][C:36]2[N:44]=[C:43]([F:45])[CH:42]=[CH:41][C:37]=2[C:38]([NH:46][C:47]2[CH:56]=[C:55]3[C:50]([CH2:51][CH2:52][C:53](=[O:58])[N:54]3[CH3:57])=[CH:49][CH:48]=2)=[O:40])[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34]1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
HATU was added to a dichloroethane solution of 2-(cyclohexylamino)-6-fluoronicotinic acid and triethylamine. After 30 minutes of stirring at room temperature, 7-amino-1-methyl-3,4-dihydroquinolin-2(1H)-one was added thereto. The reaction liquid was stirred overnight at room temperature and then hearted under reflux for 3 hours. By post-treating the reaction liquid, 2-(cyclohexylamino)-6-fluoro-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)nicotinamide was obtained.
後処理
- customThe reaction liquid
- stirringwas stirred overnight at room temperature
- temperatureunder reflux for 3 hours
- additionBy post-treating
- customthe reaction liquid
出典と根拠
- ORDレコード
- ord-77eb0c87536246de8af8a5379615cd1e
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08106190B2
反応ノート
読み込み中…