反応式
[C:1]([Cl:4])([Cl:3])=[O:2].C1(C)C=CC=CC=1.[CH3:12][O:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]([CH2:23][CH2:24][NH:25][CH2:26][CH:27]2[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]2)([CH3:22])[CH3:21])=[CH:16][CH:15]=1>C(OCC)C>[ClH:3].[CH3:12][O:13][C:14]1[CH:15]=[CH:16][C:17]([C:20]([CH2:23][CH2:24][NH:25][CH2:26][CH:27]2[CH2:32][CH2:31][N:30]([C:1]([Cl:4])=[O:2])[CH2:29][CH2:28]2)([CH3:21])[CH3:22])=[CH:18][CH:19]=1参加物
4
実験手順
To a solution of 2 M phosgene/toluene (2.0 ml, 4 mmole) in ethyl ether (20 ml) was added a solution of N-[2-(4-methoxyphenyl-1-methylethyl]-N-ethyl-(piperidin-4-ylmethyl)amine (0.23 grams, 0.79 mmole) in ethyl ether (30 ml). After 30 minutes the precipitate was collected by filtration and dried in vacuo to give N-[2-(4-methoxyphenyl-1-methylethyl]-N-ethyl-(1-chlorocarbonylpiperidin-4-ylmethyl)amine hydrochloride (0.238 grams, 77%), m.p. 144-145° C.
後処理
- filtrationAfter 30 minutes the precipitate was collected by filtration
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-1ec6e23dc6ff4907bd35a8ee02bb9891
- 出典データセット
- uspto-grants-2001_11
- 特許番号
- US06319920B1
関連ノート
読み込み中…