Trifluoroacetic acid → HCID 59253163, Verbindung
Reaktionsgleichung
FC(F)(F)C(O)=O.C(OC(=O)[NH:14][C:15]1[O:19][N:18]=[C:17]([C:20]([CH3:28])([CH3:27])[CH2:21][N:22]([C:24](=[O:26])[CH3:25])[CH3:23])[CH:16]=1)(C)(C)C>C(Cl)Cl>[NH2:14][C:15]1[O:19][N:18]=[C:17]([C:20]([CH3:28])([CH3:27])[CH2:21][N:22]([CH3:23])[C:24](=[O:26])[CH3:25])[CH:16]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Trifluoroacetic acid (0.108 mL, 1.4 mmol) is added to a solution of {3-[2-(acetyl-methyl-amino)-1,1-dimethyl-ethyl]isoxazol-5-yl}-carbamic acid tert-butyl ester (87.0 mg, 0.28 mmol) in DCM (1 mL). The reaction mixture is stirred at room temperature for 1 h. More trifluoroacetic acid (0.20 mL, 2.59 mmol) is added to the reaction mixture and the reaction mixture is stirred for another hour. After this time, the reaction mixture is diluted with DCM and quenched with saturated aqueous NaHCO3 solution. The layers are separated and the aqueous layer is extracted with DCM twice. The organics are combined and washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to provide 28.0 mg of the title compound. Yield: 47%. LC-MS Retention time: 0.94 mins. ESI+ion mode. Zorbax SB-C18 column (3.5 μm, 4.6×30 mm). Gradient: 5% B to 80% B (0 min to 1.7 mins), 80% B to 95% B (1.7 mins to 2 mins), 95% B to 95% B (2 mins to 2.1 mins). Flow rate: 2.5 mL/min. A=(Water+0.1% Formic Acid) B=(Acetonitrile+0.1% Formic Acid). Diode Array Detector; m/z 212 [M+H].