Hydrochloric Acid → HCID 69030132, Verbindung
Reaktionsgleichung
[ClH:1].[CH2:2]([N:6]([CH2:41][CH:42]([CH3:44])[CH3:43])[C:7]([C:9]1[CH:40]=[CH:39][C:12]2[N:13]([CH2:29][CH2:30][NH:31]C(=O)OC(C)(C)C)[C:14]([NH:16][C:17]3[CH:22]=[C:21]([O:23][CH3:24])[C:20]([O:25][CH3:26])=[C:19]([O:27][CH3:28])[CH:18]=3)=[N:15][C:11]=2[CH:10]=1)=[O:8])[CH:3]([CH3:5])[CH3:4]>C(OCC)(=O)C>[ClH:1].[NH2:31][CH2:30][CH2:29][N:13]1[C:12]2[CH:39]=[CH:40][C:9]([C:7]([N:6]([CH2:2][CH:3]([CH3:4])[CH3:5])[CH2:41][CH:42]([CH3:44])[CH3:43])=[O:8])=[CH:10][C:11]=2[N:15]=[C:14]1[NH:16][C:17]1[CH:22]=[C:21]([O:23][CH3:24])[C:20]([O:25][CH3:26])=[C:19]([O:27][CH3:28])[CH:18]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A stream of dry HCl is passed through a solution of tert-butyl 2-{5-[(diisobutylamino)carbonyl]-2-[(3,4,5-trimethoxy phenyl)amino]-1H-benzimidazol-1-yl}ethylcarbamate (2.56 g, prepared according to the procedure described in Example A1, reaction diagram A) in ethyl acetate (100 ml), (100% ethyl acetate) cooled down to 0° C. until the TLC shows complete disappearance of the starting product. The resulting mixture is then evaporated under reduced pressure. The solid obtained is triturated in diethylether and filtered in order to produce the expected compound in the form of white crystals (2.25 g, 97% yield).