2-Methoxyethylamine → Ethyl 5-bromo-2-((2-methoxyethyl)amino)pyrimidine-4-carboxylate
Reaktionsgleichung
[CH3:1][O:2][CH2:3][CH2:4][NH2:5].[CH2:6]([O:8][C:9]([C:11]1[C:16]([Br:17])=[CH:15][N:14]=[C:13](S(C)(=O)=O)[N:12]=1)=[O:10])[CH3:7]>ClCCl>[CH2:6]([O:8][C:9]([C:11]1[C:16]([Br:17])=[CH:15][N:14]=[C:13]([NH:5][CH2:4][CH2:3][O:2][CH3:1])[N:12]=1)=[O:10])[CH3:7]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2-Methoxyethylamine (0.278 ml, 3.2 mmol) was added at room temperature to a solution of 5-bromo-2-methanesulfonyl-pyrimidine-4-carboxylic acid ethyl ester (0.2 g, 0.65 mmol) in dichloromethane (5 ml). Stirring was continued at 45° C. for 2 hours. The solvent was evaporated and the crude product was purified by silica gel chromatography using an ethyl acetate/heptane eluent to yield the title compound as colorless oil (0.175 g, 89%).