Hydrochloric Acid → {4-[(4S,5R)-2-(6-tert-Butyl-4-ethoxy-pyridin-3-yl)-4,5-bis-(4-chloro-phenyl)-4,5-dimethyl-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-acetic acid hydrochloride

HRID 1894411

Reaktionsgleichung

Reaktionsgleichung von HRID 1894411
C([O:5][C:6](=[O:50])[CH2:7][N:8]1[CH2:13][CH2:12][N:11]([C:14]([N:16]2[C@@:20]([C:22]3[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][CH:23]=3)([CH3:21])[C@@:19]([C:30]3[CH:35]=[CH:34][C:33]([Cl:36])=[CH:32][CH:31]=3)([CH3:29])[N:18]=[C:17]2[C:37]2[CH:38]=[N:39][C:40]([C:46]([CH3:49])([CH3:48])[CH3:47])=[CH:41][C:42]=2[O:43][CH2:44][CH3:45])=[O:15])[CH2:10][CH2:9]1)(C)(C)C.[OH-].[Li+].Cl>CO.O1CCCC1>[ClH:28].[C:46]([C:40]1[N:39]=[CH:38][C:37]([C:17]2[N:16]([C:14]([N:11]3[CH2:10][CH2:9][N:8]([CH2:7][C:6]([OH:50])=[O:5])[CH2:13][CH2:12]3)=[O:15])[C@@:20]([C:22]3[CH:23]=[CH:24][C:25]([Cl:28])=[CH:26][CH:27]=3)([CH3:21])[C@@:19]([C:30]3[CH:31]=[CH:32][C:33]([Cl:36])=[CH:34][CH:35]=3)([CH3:29])[N:18]=2)=[C:42]([O:43][CH2:44][CH3:45])[CH:41]=1)([CH3:47])([CH3:48])[CH3:49]

Komponenten

6

Versuchsvorschrift

{4-[(4S,5R)-2-(6-tert-Butyl-4-ethoxy-pyridin-3-yl)-4,5-bis-(4-chloro-phenyl)-4,5-dimethyl-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-acetic acid tert-butyl ester was either reacted with lithium hydroxide (2N solution) in methanol and tetrahydrofuran at 50° C. for 4 h or with 1N hydrochloric acid at 50° C. for 2.5 h to give the title compound. HR-MS (ES, m/z) calculated for C35H42Cl2N5O4 [(M+H)+] 666.2609, observed 666.2611.

Quellen und Nachweise

ORD-Eintrag
ord-121a4ee0cff74c85bdcc0d609cd8385a
Quelldatensatz
uspto-grants-2013_08
Patentnummer
US08513239B2

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