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Chemical Compound Review

PubChem15371     pyridine-2,6-diamine

Synonyms: SureCN64599, CHEMBL339234, NSC-1921, CCRIS 6682, D24404_ALDRICH, ...
 
 
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Disease relevance of 1/C5H7N3/c6-4-2-1-3-5(7)8-4/h1-3H,(H4,6,7,8

 

High impact information on 1/C5H7N3/c6-4-2-1-3-5(7)8-4/h1-3H,(H4,6,7,8

  • 2,6-Diaminopyridine is very readily dibenzylated at the 3,5 positions as well as on an amino group, by a phenolic Mannich base; use of a fourfold excess of the pyridine provided a 3-benzylated 2,6-diaminopyridine in 50% yield; this was inactive as an inhibitor of dihydrofolate reductase at 10(-4) M [2].
  • The new 1,10-phenanthroline containing 1:1 proton-transfer compound LH(2), [pyda.H(2)](2+)[phendc](2-), was synthesized from the reaction of 2,6-pyridinediamine, pyda, and 1,10-phenanthroline-2,9-dicarboxylic acid, phendc.H(2), and characterized by elemental analysis, ES-Ms, IR, (1)H, (13)C NMR, and UV/vis spectroscopies [3].
 

Analytical, diagnostic and therapeutic context of 1/C5H7N3/c6-4-2-1-3-5(7)8-4/h1-3H,(H4,6,7,8

References

 
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