5-Chloro-alpha,alpha-dimethyl-1H-indole-3-ethanamine → [2-(6-fluoro-1H-indol-3-yl)-1,1-dimethylethyl]{2-[2-(2-methyl-prop-1-yloxy)phenoxy]ethyl}amine hydrochloride
反応式
CS(O[CH2:6][CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[O:15][CH2:16][CH:17]([CH3:19])[CH3:18])(=O)=O.[Cl:20]C1C=C2C(=CC=1)NC=C2CC(N)(C)C.[F:35][C:36]1[CH:44]=[C:43]2[C:39]([C:40]([CH2:45][C:46]([NH2:49])([CH3:48])[CH3:47])=[CH:41][NH:42]2)=[CH:38][CH:37]=1>>[ClH:20].[F:35][C:36]1[CH:44]=[C:43]2[C:39]([C:40]([CH2:45][C:46]([NH:49][CH2:6][CH2:7][O:8][C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[O:15][CH2:16][CH:17]([CH3:18])[CH3:19])([CH3:47])[CH3:48])=[CH:41][NH:42]2)=[CH:38][CH:37]=1参加物
4
反応物 3
生成物 1
実験手順
Proceeding as an Example 3, but replacing 2-[2-(cyclopropylmethyloxy)phenoxy]ethyl methanesulfonate with 2-[2-(2-methylprop-1-yloxy)phenoxy]ethyl methanesulfonate and [2-(5-chloro-1H-indol-3-yl)-1,1-dimethylethyl]amine with [2- (6-fluoro-1H-indol-3-yl)-1,1-dimethylethyl]amine, gave [2-(6-fluoro-1H-indol-3-yl)-1,1-dimethylethyl]{2-[2-(2-methyl-prop-1-yloxy)phenoxy]ethyl}amine hydrochloride, m.p. 135°-137° C.