142272-00-2

Upstream product

• 39565-07-6 7-amino-2,4-dimethyl-1,8-naphthyridine 
• 403-29-2 2-bromo-4'-fluoroacetophenone 

Downstream Products

• 142272-09-1 1-amino-6,8-dimethyl-2-(4-fluorophenyl)imidazo<1,2-a><1,8>naphthyridine 
• 142272-08-0 2-isocyano-5,7-dimethyl<1,8>naphthyridine 
• 142272-07-9 1-chloro-6,8-dimethyl-2-(4-fluorophenyl)imidazo<1,2-a><1,8>naphthyridine 
• 142272-06-8 6,8-dimethyl-1-nitroso-2-(4-fluorophenyl)imidazo<1,2-a><1,8>naphthyridine 

Relevant academic research and scientific papers

Synthesis, structure and reactivity of imidazo[1,2-a] [1,8]naphthyridines

The synthesis and reactivity of imidazo[1,2-a][1,8]naphthyridines are reported. Electrophilic substitution reactions were studied and the site of the reaction was established with the aid of high-field 1H and 13C nmr spectra. The experimental C-1 position reaction was correlated with a CNDO/2 calculations.

Carbon-Nitrogen Bond Formation in Cyclisation by Deoxygenation, Thermolysis or Photolysis of Phenylimidazonaphthyridines

Triethyl phosphite deoxygenation of 2-(2-nitrophenyl)imidazonaphthyridine (3) led to the C-insertion to give the indoloimidazonaphthyridine 5.Our attempt to promote the N-insertion by blocking the C-3 position failed.Triethyl phosphite deoxyge