[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:24]=[C:25]([O:27][CH3:28])[CH:26]=1)[CH2:6][NH:7][C@@H:8]([CH3:23])[C@@H:9]([C:11]1[CH:12]=[CH:13][C:14]([OH:22])=[C:15]([NH:17][S:18]([CH3:21])(=[O:20])=[O:19])[CH:16]=1)[OH:10].[ClH:29].O1CCOCC1>O1CCOCC1>[ClH:29].[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:24]=[C:25]([O:27][CH3:28])[CH:26]=1)[CH2:6][NH:7][C@@H:8]([CH3:23])[C@@H:9]([C:11]1[CH:12]=[CH:13][C:14]([OH:22])=[C:15]([NH:17][S:18]([CH3:21])(=[O:20])=[O:19])[CH:16]=1)[OH:10]To the dioxane solution (1 mL) of the obtained amine (5) (47 mg, 0.11 mmol) was added 4N hydrochloric acid/dioxane solution (0.04 mL) and the resulting mixture was freeze-dried to obtain hydrochloric acid salt of the amine (5) as a white solid (27 mg, Yield: 55%).
Wird geladen…