Aminopyrimidines and derivatives. XIII. Condensation of 4-aminopyrimidines with aldoses was written by Asenjo Asenjo, R.;Melgarejo Sampedro, M.;Rodriguez Melgarejo, C.;Nogueras Montiel, M.;Sanchez Rodrigo, A.. And the article was included in Anales de Quimica, Serie C: Quimica Organica y Bioquimica in 1983.Electric Literature of C6H9N3OS This article mentions the following:
Several N-glycosides I (R = H, Me; R1 = H, CH2OH; R2 = H; X = O,S) were obtained by reaction of 4-aminopyrimidines II with glucose and xylose. I (R2 = Ac) are obtained by acetylation of I (R2 = H) with Ac2O and pyridine at room temperature In the experiment, the researchers used many compounds, for example, 6-Amino-3-methyl-2-(methylthio)pyrimidin-4(3H)-one (cas: 54030-56-7Electric Literature of C6H9N3OS).
6-Amino-3-methyl-2-(methylthio)pyrimidin-4(3H)-one (cas: 54030-56-7) belongs to pyrimidine derivatives. Pyrimidine also found in many synthetic compounds such as barbiturates and the HIV drug, zidovudine. For example, the neurotoxin tetrodotoxin is a pyrimidine derivative. It is found in a number of species including the Japanese puffer fish, the blue-ringed octopus, and the orange-bellied newt. Tetrodotoxin prevents the transmission of nerve signals and can result in paralysis and death.Electric Literature of C6H9N3OS
Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia