Hydrochloric Acid → HCID 131727849, Verbindung
Reaktionsgleichung
[ClH:1].C(OC([N:9]1[CH2:16][CH:15]2[O:17][CH:11]([CH2:12][N:13]([CH2:18][CH2:19][NH:20][S:21]([C:24]3[CH:29]=[CH:28][C:27]([F:30])=[CH:26][CH:25]=3)(=[O:23])=[O:22])[CH2:14]2)[CH2:10]1)=O)(C)(C)C>O1CCOCC1>[ClH:1].[F:30][C:27]1[CH:28]=[CH:29][C:24]([S:21]([NH:20][CH2:19][CH2:18][N:13]2[CH2:14][CH:15]3[O:17][CH:11]([CH2:10][NH:9][CH2:16]3)[CH2:12]2)(=[O:23])=[O:22])=[CH:25][CH:26]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
HCl in dioxane (50 ml) was added to a solution of 7-[2-(4-Fluoro-benzenesulfonylamino)-ethyl]-9-oxa-3,7-diaza-bicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester (4 g; see step (ii) above) in dry dioxane (50 ml) at RT and the reaction mixture was stirred at RT for 1 h. Dioxane was decanted, precipitated solid was washed with dry diethyl ether (three times) and dried under vacuum to give the title compound as pale yellow solid. Yield: 3.55 g