Publication | Closed Access
Synthesis of 2,3‐dihydropyrido‐ and 2,3‐dihydropyrimido‐[1,4]diazepines from triaminopyridine and triaminopyrimidine
15
Citations
6
References
1997
Year
Selective 13BiochemistryNatural SciencesDiversity-oriented SynthesisOrganic ChemistryNmr TechniquesChemistryHeterocycle ChemistryDerivative (Chemistry)Synthetic ChemistryAcetic Acid
Abstract The reaction of 2,3,6‐triaminopyridine 1 and 4,5,6‐triaminopyrimidine 2 with one equivalent of the chal‐cones 3, in acetic acid, leads to the formation of the 8‐amino‐2,3‐dihydro‐1 H ‐pyrido[2,3‐ b ][1,4]diazepine and 6‐amino‐2,3‐dihydro‐1 H ‐pyrimido[4,5‐ b ][1,4]diazepine derivatives 4 and 5 . The products were characterized by NMR techniques such as 13 C, 1 H, and DEPT including selective 13 C{ 1 H} decoupling experiments.
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