Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 3680-71-5, Name is 1,7-Dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one, SMILES is O=C1C2=C(NC=C2)NC=N1, in an article , author is Sirakanyan, Samvel N., once mentioned of 3680-71-5, Name: 1,7-Dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one.
Synthesis and antimicrobial evaluation of novel polyheterocyclic systems derived from cyclopenta[4 ‘,5 ‘]pyrido[3 ‘,2 ‘:4,5]furo[3,2-d]pyrimidine
The synthesis of new cyclopenta[4′,5′]pyrido[3′,2’:4,5]furo[3,2-d]pyrimidin-7-amines have been carried out to study their antimicrobial activity. The biological tests evidenced that some of the synthesized compounds exhibit pronounced antimicrobial properties. A study of the structure-activity relationship revealed that the 3,5-dimethyl-1H-pyrazol-1-yl moiety linked to the carbon C-9 of the pyrimidine plays a decisive role in the manifestation of activity. The influence of 3,5-dimethyl-1H-pyrazol-1-yl group on the Dimroth rearrangement and azide-tetrazole equilibrium has also been examined.
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Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia