Trifluoroacetic acid → 1-(2-Amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea
Reaktionsgleichung
[NH2:1][C:2]([CH3:30])([CH3:29])[CH2:3][NH:4][C:5](=[O:28])[NH:6][C:7]1[CH:26]=[CH:25][C:10]([CH2:11][CH:12]2[CH2:17][CH2:16][N:15](C(OC(C)(C)C)=O)[CH2:14][CH2:13]2)=[CH:9][C:8]=1[F:27].FC(F)(F)C(O)=O>ClCCl>[NH2:1][C:2]([CH3:30])([CH3:29])[CH2:3][NH:4][C:5]([NH:6][C:7]1[CH:26]=[CH:25][C:10]([CH2:11][CH:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)=[CH:9][C:8]=1[F:27])=[O:28]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
tert-Butyl 4-(4-(3-(2-amino-2-methylpropyl)ureido)-3-fluorobenzyl)piperidine-1-carboxylate (2.272 mmol, 960 mg) was dissolved in dichloromethane (40 mL) and trifluoroacetic acid (45.4 mmol, 5181 mg) added. The mixture was stirred at room temperature for 3 hours before concentrating under reduced pressure. The resulting residue was purified by strong cation exchange column chromatography to afford the title compound (110 mg). MS (ESI) m/z 323.5 [M+H]+