What unique challenges do researchers face in 16710-11-5

As far as I know, this compound(16710-11-5)Application In Synthesis of 4-Methyl-6-(methylthio)pyrimidin-2-ol can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 16710-11-5, is researched, SMILESS is CSC1=NC(O)=NC(C)=C1, Molecular C6H8N2OSJournal, Russian Journal of General Chemistry called 4-arylamino-2-(2-acetoxyethyl)amino-6-methylpyrimidines: Synthesis, deacetylation, and biological activity, Author is Erkin, A. V.; Krutikov, V. I., the main research direction is ethanolamine acetate arylaminopyrimidinyl tuberculostatic preparation; pyrimidinediamine acetoxyethyl aryl tuberculostatic preparation; deacetylation acetoxyethylaminopyrimidine.Application In Synthesis of 4-Methyl-6-(methylthio)pyrimidin-2-ol.

The reaction of 2-(2-acetoxyethyl)amino-4-chloro-6-methylpyrimidine with aromatic amines leads to a series of 4-arylamino-2-(2-acetoxyethyl)amino-6-methylpyrimidines. Deacetylation of these compounds proceeds in both acidic and basic media. Most of the (arylamino)pyrimidines obtained exhibit a pronounced antituberculous effect.

As far as I know, this compound(16710-11-5)Application In Synthesis of 4-Methyl-6-(methylthio)pyrimidin-2-ol can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Reference:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem