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The Preparation Of 3,4-Diaminopyridine, Emil John Fencl

Theses

The preparation of 3,4-diamincpyridine from pyridine was investigated, but found to be of little synthetic value because of the low yield obtained on the rearrangement of 4-nitraminopyridine to 3-nitro 4-aminopyridine. In attempt to nitrate nicotinamide-N-oxide resulted in the isolation of nicotinic acid-N-oxide. Attempts to nitrate nicotinic acid-N-oxide were unsuccessful. Attempts to oxidize 3-methylpyridine-N-oxide and 4-nitro-3-methylpyridine were unsuccessful. The nitration of 3-methylpyridine-N-oxide led to the isolation of 2-nitro-5-methylpyridine, which has not previously been reported as a by-product of that reaction.