Trifluoroacetic acid → 2-[2-(3,5-Difluoro-benzylcarbamoyl)-propionylamino]-3-(1H-indol-3-yl)-propionic acid
Reaktionsgleichung
C([O:5][C:6](=[O:35])[CH:7]([NH:18][C:19](=[O:34])[CH:20]([C:22](=[O:33])[NH:23][CH2:24][C:25]1[CH:30]=[C:29]([F:31])[CH:28]=[C:27]([F:32])[CH:26]=1)[CH3:21])[CH2:8][C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[NH:11][CH:10]=1)(C)(C)C.FC(F)(F)C(O)=O>ClCCl>[F:32][C:27]1[CH:26]=[C:25]([CH:30]=[C:29]([F:31])[CH:28]=1)[CH2:24][NH:23][C:22]([CH:20]([CH3:21])[C:19]([NH:18][CH:7]([CH2:8][C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[NH:11][CH:10]=1)[C:6]([OH:35])=[O:5])=[O:34])=[O:33]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2-[2-(3,5-Difluoro-benzylcarbamoyl)-propionylamino]-3-(1H-indol-3-yl)-propionic acid tert-butyl ester (5.99 g, 12.3 mmol) was dissolved in dichloromethane (15 ml), and trifluoroacetic acid (15 ml) was added at 0° C. The mixture was stirred overnight at r.t. until all starting material was consumed (analytical HPLC). The volatiles were evaporated, the residue was taken up in ethyl acetate and washed with water. The organic layers were dried (Na2SO4). After evaporation of the solvent, the title compound, MS: m/e=429.4 (M+H+), (3.5 g, 66%) was obtained by chromatographic purification of the residue (silica gel, MeOH, CH2Cl2).