Unfused heterobicycles as amplifiers of phleomycin. II. Some 2,4′-, 4,5′- and 5,5′-bipyrimidines was written by Brown, Desmond J.;Cowden, William B.;Strekowski, Lucjan. And the article was included in Australian Journal of Chemistry in 1981.Quality Control of 2-Chloropyrimidine-4-carbonitrile This article mentions the following:
Methoxy, methylthio, dimethylamino, ็?dimethylaminoethylamino, and ็?dimethylaminoethylthio substituted 2,4′-, 4,5′- and 5,5′-bipyrimidines were prepared Thus, the pyrimidine I (R = Cl, R1 = CN) was treated with Me2NH and the resulting I (R = Me2N, R1 = CN) treated with PhSO3–.NH4+ to give I (R = Me2N, R1 = C(:NH)NH2).PhSO3H, which was cyclized with H2C(CO2Me)2 to give the bipyrimidine II. II was chlorinated by POCl3 and then treated with Me2NH and Me2NCH2CH2NH2 to give the bipyrimidine III. In the experiment, the researchers used many compounds, for example, 2-Chloropyrimidine-4-carbonitrile (cas: 75833-38-4Quality Control of 2-Chloropyrimidine-4-carbonitrile).
2-Chloropyrimidine-4-carbonitrile (cas: 75833-38-4) belongs to pyrimidine derivatives. The pyrimidine ring system has wide occurrence in nature as substituted and ring fused compounds and derivatives. We all know its importance to life – pyrimidine and purine bases are included in the structure of DNA and RNA.Quality Control of 2-Chloropyrimidine-4-carbonitrile
Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia