Chemistry Heterocyclic Building Blocks Naphthyridines
Naphthyridine, which has a chemical formula of C8H6N2, belongs to a group of diazanaphthalenes called isomeric naphthyridines. This particular naphthyridine is the most extensively researched among the six isomers.
There are various marine products that contain functionalized naphthyridines and their benzo/heterofused analogs. These compounds have been found to exhibit diverse properties, including anti-proliferative and anti-aggressive effects, as well as inhibition of HIV-1 integrase. Additionally, they are employed as anti-HCV agents.
Due to the presence of nitrogen atoms, the naphthyridines exhibit electron drift in their molecular orbitals, resulting in distortion of each of the five orbitals. These orbitals contain 10 delocalized π-electrons.
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tert-Butyl 7-chloro-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxylate
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tert-Butyl (8-chloro-1,7-naphthyridin-3-yl)carbamate
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1,2,3,4-Tetrahydro-2,6-naphthyridine dihydrochloride
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tert-Butyl 2-(Hydroxymethyl)-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate
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5,7-Bis(trifluoromethyl)-1,8-naphthyridin-2-amine
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2,4-Bis(trifluoromethyl)imidazo[1,2-a][1,8]naphthyridine-8-carbohydrazide
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4-(6-(Azetidin-1-yl)-2-methyl-1-oxo-1,2-dihydro-2,7-naphthyridin-4-yl)-2,6-dimethoxybenzaldehyde
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5,6,7,8-Tetrahydro-1,6-naphthyridine-3-carbonitrile hydrochloride