TY - JOUR
T1 - (S)-(+)-ketamine hydrochloride
AU - Hakey, Patrick
AU - Ouellette, Wayne
AU - Zubieta, Jon
AU - Korter, Timothy
PY - 2008
Y1 - 2008
N2 - The crystal structure of the title compound {systematic name: (S)-(+)-N-[1-(2-chloro-phen-yl)-2-oxocyclo-hexyl]meth-anam-in-ium chloride}, C13H17ClNO+·Cl-, was determined at 90 (2) K. The (S)-(+)-ketamine hydro-chloride salt is a well known anesthetic compound and is dramatically more potent than its R isomer. In the title compound, the cyclo-hexa-none ring adopts a chair conformation with the oxo group in the equatorial orientation. The methyl-amino and 2-chloro-phenyl groups at the 2-position have an equatorial and an axial orientation, respectively. The packing of ions is stabilized by an infinite one-dimensional ⋯Cl⋯H - N - H⋯Cl⋯ hydrogen-bonding network, involving NH2 + groups as donors and chloride anions as acceptors.
AB - The crystal structure of the title compound {systematic name: (S)-(+)-N-[1-(2-chloro-phen-yl)-2-oxocyclo-hexyl]meth-anam-in-ium chloride}, C13H17ClNO+·Cl-, was determined at 90 (2) K. The (S)-(+)-ketamine hydro-chloride salt is a well known anesthetic compound and is dramatically more potent than its R isomer. In the title compound, the cyclo-hexa-none ring adopts a chair conformation with the oxo group in the equatorial orientation. The methyl-amino and 2-chloro-phenyl groups at the 2-position have an equatorial and an axial orientation, respectively. The packing of ions is stabilized by an infinite one-dimensional ⋯Cl⋯H - N - H⋯Cl⋯ hydrogen-bonding network, involving NH2 + groups as donors and chloride anions as acceptors.
UR - http://www.scopus.com/inward/record.url?scp=49149090400&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=49149090400&partnerID=8YFLogxK
U2 - 10.1107/S1600536808021053
DO - 10.1107/S1600536808021053
M3 - Article
C2 - 21203199
AN - SCOPUS:49149090400
SN - 1600-5368
VL - 64
SP - o1487
JO - Acta Crystallographica Section E: Structure Reports Online
JF - Acta Crystallographica Section E: Structure Reports Online
IS - 8
ER -