Pyrazole studies. 21. Synthesis of 3-dialkylaminomethyl-5-methyl-4-substituted-1H-pyrazoles. Selective functionalization of one methyl group via N-nitration of 3,5-dimethyl-4-substituted-1H-pyrazoles was written by Lammers, H.;Vollinga, R.;Zandbergen, P.;Cohen-Fernandes, P.;Habraken, C. L.. And the article was included in Journal of Heterocyclic Chemistry in 1995.Synthetic Route of C5H7ClN2 This article mentions the following:
Treatment of 3,5-dimethyl-1,4-dinitro-1H-pyrazole and 4-halo-3,5-dimethyl-1-nitro-1H-pyrazoles with secondary amines in acetonitrile, in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), gave 3-[(dialkylamino)methyl]-1H-pyrazoles in good to excellent yields. In this way one of the, in general, inert Me groups of 3,5-dimethyl-4-substituted-1H-pyrazoles is functionalized creating a new synthetic route to azoles containing a coordinating substituent. In the experiment, the researchers used many compounds, for example, 4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8Synthetic Route of C5H7ClN2).
4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8) belongs to pyrazole derivatives. The 1H-pyrazole provides an excellent means by which to provide the requisite hydrogen bond acceptor–donor motifs, whether as a monocyclic ring or as a fused indazole ring. Pyrazoles and pyrimidines have diverse biological and pharmacological activities. There are a number of antimicrobial compounds containing pyrazole moiety as the core unit. Pyrazofurin is important antimicrobial drug and 2-methylpyrimidine-4-ylamine derivatives I and II were found to be effective inhibitors of Escherichia coli PDHc-E1 with antibacterial and antifungal activity.Synthetic Route of C5H7ClN2
Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics