Hydrochloric Acid → 2-{(S)-1-[(3S,45)-3-(4-Chloro-phenyl)-piperidin-4-yl]-ethoxy}-5-trifluoromethyl-pyridine

反応式

ClC1C=CC(OCC2CCNCC2C2C=CC(Cl)=CC=2)=NC=1.Cl.C([N:31]1[CH2:36][CH2:35][C@H:34]([C@@H:37]([O:39][C:40]2[CH:45]=[CH:44][C:43]([C:46]([F:49])([F:48])[F:47])=[CH:42][N:41]=2)[CH3:38])[C@@H:33]([C:50]2[CH:55]=[CH:54][C:53]([Cl:56])=[CH:52][CH:51]=2)[CH2:32]1)C1C=CC=CC=1>>[Cl:56][C:53]1[CH:54]=[CH:55][C:50]([C@@H:33]2[C@@H:34]([C@@H:37]([O:39][C:40]3[CH:45]=[CH:44][C:43]([C:46]([F:48])([F:47])[F:49])=[CH:42][N:41]=3)[CH3:38])[CH2:35][CH2:36][NH:31][CH2:32]2)=[CH:51][CH:52]=1

参加物

反応物 3

HCID 313Hydrochloric Acid2 回

HCID 594381752-{(S)-1-[(3S,4S)-1-Benzyl-3-(4-chloro-phenyl)-piperidin-4-yl]-ethoxy}-5-trifluoromethyl-pyridine

HCID 712055575-chloro-2-[(3RS, 4RS)-3-(4-chloro-phenyl)-piperidin-4-ylmethoxy]-pyridine

生成物 1

HCID 594381202-{(S)-1-[(3S,45)-3-(4-Chloro-phenyl)-piperidin-4-yl]-ethoxy}-5-trifluoromethyl-pyridine

実験手順

In analogy to the procedure described for the synthesis of 5-chloro-2-[(3RS, 4RS)-3-(4-chloro-phenyl)-piperidin-4-ylmethoxy]-pyridine; hydrochloride (example 1, step h) the title compound was prepared from 2-{(S)-1-[(3S,4S)-1-Benzyl-3-(4-chloro-phenyl)-piperidin-4-yl]-ethoxy}-5-trifluoromethyl-pyridine as off-white foam as the respective HCl salt. MS (m/e): 385.2 [(M+H)+].