CN(C)C1=NC=C(C=C1)[C@H]1C[C@@H]2CC[C@H]1N2S(=O)(=O)C1=CC=C(C)C=C1

InChIKey=KCCURUHDHYZBDI-QXAKKESOSA-N

C20H25N3O2S

371.5

Organic compounds

Alkaloids and derivatives

Epibatidine analogues

Not available

Not available

Epibatidine analogues

N,N-disubstituted p-toluenesulfonamides Pyrrolidinylpyridines Benzenesulfonamides Benzenesulfonyl compounds Dialkylarylamines Aminopyridines and derivatives Organosulfonamides Imidolactams Sulfonyls Pyrrolidines Heteroaromatic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Epibatidine-skeleton - N,n-disubstituted p-toluenesulfonamide - P-toluenesulfonamide - Pyrrolidinylpyridine - Benzenesulfonamide - Tosyl compound - Benzenesulfonyl group - Dialkylarylamine - Aminopyridine - Toluene - Monocyclic benzene moiety - Pyridine - Organosulfonic acid amide - Imidolactam - Benzenoid - Heteroaromatic compound - Pyrrolidine - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Amine - Organosulfur compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as epibatidine analogues. These are compounds containing an epibatidine moiety, with a structure characterized by a 2-chloropyridine moiety connected to an 7-azabicyclo[2.2.1]heptane in exo position.

Not available