CN1C2=CC=CC=C2N2C1=C(C(=O)NCCN1CCCC1)C(=O)C1=C2N=C(Cl)C=C1

InChIKey=VEGQEOJYWGHKOF-UHFFFAOYSA-N

C22H22ClN5O2

423.9

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

Benzimidazoles Imidazo[1,2-a]pyridines Pyridinecarboxylic acids and derivatives 2-halopyridines Aryl chlorides Benzenoids N-alkylpyrrolidines N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Secondary carboxylic acid amides Trialkylamines Amino acids and derivatives Azacyclic compounds Hydrocarbon derivatives Organic oxides Organochlorides Organooxygen compounds

Aromatic heteropolycyclic compounds

Naphthyridine - Imidazo[1,2-a]pyridine - Benzimidazole - Pyridine carboxylic acid or derivatives - 2-halopyridine - Aryl chloride - Aryl halide - N-substituted imidazole - Pyridine - Benzenoid - N-alkylpyrrolidine - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carboxamide group - Amino acid or derivatives - Azacycle - Carboxylic acid derivative - Organooxygen compound - Hydrocarbon derivative - Organohalogen compound - Organic oxide - Amine - Organic nitrogen compound - Organic oxygen compound - Organochloride - Organonitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as naphthyridines. These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.

Not available