A CONVENIENT ROUTE TO CYANO DERIVATIVES OF BENZONAPHTHYRIDINES
DOI:
https://doi.org/10.1007/2106Keywords:
benzonaphthyridine N-oxides, carbonitriles, carboxylic acids, cyanationAbstract
A smooth synthesis of benzo[c][1,5]naphtyridine-6-carbonitrile and benzo[h][1,6]naphthyridine-5-carbonitrile, starting from benzonaphthyridine N-oxides, is achieved by treatment with trimethylsilane carbonitrile (Me3SiCN) in CH2Cl2 at 0–5°C. The resulting nitriles are then hydrolyzed to corresponding acids by boiling in aqueous alkali.
How to Cite
Bachowska, B. Chem. Heterocycl. Compd. 2011, 47(3), 332. [Khim. Geterotsikl. Soedin. 2011, 406.]