Ammonium → HCID 481003, Verbindung

Reaktionsgleichung

Cl.[CH3:2][C:3]1[CH:4]=[C:5]([CH:25]=[C:26]([CH3:28])[CH:27]=1)[CH2:6][C:7]1[C:12]([CH2:13][CH3:14])=[C:11]([CH3:15])[N:10]=[C:9]([O:16]C)[C:8]=1[NH:18]C(=O)C(C)(C)C.[NH4+]>O>[NH2:18][C:8]1[C:9](=[O:16])[NH:10][C:11]([CH3:15])=[C:12]([CH2:13][CH3:14])[C:7]=1[CH2:6][C:5]1[CH:4]=[C:3]([CH3:2])[CH:27]=[C:26]([CH3:28])[CH:25]=1

Komponenten

Versuchsvorschrift

3M aqueous hydrochloric acid (150 mL) was added to a suspension of 4-(3,5-dimethylbenzyl)-5-ethyl-2-methoxy-6-methyl-3-pivaloylaminopyridine (2.36 g) in water (300 mL). The mixture was refluxed for 3.5 h and then stirred at room temperature for 12 h. The solution was basified by adding concentrated ammonium hydroxyde and was extracted with 3×800 mL ethyl acetate. The combined organic layers were washed with 110 mL brine, dried over magnesium sulfate and concentrated under reduced pressure giving 3-amino-4-(3,5-dimethylbenzyl)-5-ethyl-6-methylpyridin-2(1H)-one. (1.79 g, 100%). mp 204-205° C.