Cc1cc2c(cnc(NC3CCN(CC3)C(=O)C(F)(F)CN)c2[nH]c1=O)C1=CCOCC1

InChIKey=YTQRBAXLTKDECT-UHFFFAOYSA-N

C22H27F2N5O3

447.487

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

N-acylpiperidines Polyhalopyridines Secondary alkylarylamines Pyridinones 2-halopyridines Pyrans Imidolactams Tertiary carboxylic acid amides Heteroaromatic compounds Lactams Amino acids and derivatives Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organofluorides Organic oxides Monoalkylamines Hydrocarbon derivatives Alkyl fluorides

Aromatic heteropolycyclic compounds

Naphthyridine - N-acyl-piperidine - Polyhalopyridine - 2-halopyridine - Secondary aliphatic/aromatic amine - Pyridinone - Imidolactam - Pyridine - Pyran - Piperidine - Heteroaromatic compound - Tertiary carboxylic acid amide - Lactam - Carboxamide group - Amino acid or derivatives - Oxacycle - Azacycle - Secondary amine - Ether - Dialkyl ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Primary aliphatic amine - Amine - Alkyl halide - Alkyl fluoride - 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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