Reaktion #1869184

Reaktionsgleichung

methanesulphonyl chloride

trifluoromethanesulphonic anhydride

quinoline

4-hydroxy-[1,5]naphthyridine

→

4-amino 1,5-naphthyridine

n-propylamine

Lösungsmittel

pyridine

phosphorus oxychloride

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigewith subsequent hydrolysis to the acid

Vorschrift

4-Hydroxy-1,5-naphthyridines can be prepared from 3-aminopyridine derivatives by reaction with diethyl ethoxymethylene malonate to produce the 4-hydroxy-3-carboxylic acid ester derivative with subsequent hydrolysis to the acid, followed by thermal decarboxylation in quinoline (as for example described for 4-Hydroxy-[1,5]naphthyridine-3-carboxylic acid, J. T. Adams et al., J. Amer. Chem. Soc., 1946, 68, 1317). A 4-hydroxy-[1,5]naphthyridine can be converted to the 4-chloro derivative by heating in phosphorus oxychloride, or to the 4-methanesulphonyloxy or 4-trifluoromethanesulphonyloxy derivative by reaction with methanesulphonyl chloride or trifluoromethanesulphonic anhydride, respectively, in the presence of an organic base. A 4-amino 1,5-naphthyridine can be obtained from the 4-chloro derivative by reaction with n-propylamine in pyridine.

Quelle