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Absolute configuration of the enantiomers of 7-chloro-4-[[4-(diethylamino)-1-methylbutyl]amino]quinoline (chloroquine)

✍ Scribed by Craig, J. Cymerman; Bhargava, Hemendra N.; Everhart, E. Thomas; LaBelle, Bruce; Ohnsorge, Ulrich; Webster, Richard V.


Book ID
118165240
Publisher
American Chemical Society
Year
1988
Tongue
English
Weight
580 KB
Volume
53
Category
Article
ISSN
0022-3263

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Resolution of 7-chloro-4(4β€²-diethylamino
✍ Dr. J. Cymerman Craiga; Aslam M. Ansari πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 300 KB

## Abstract Evidence is accumulating that 7‐chloro‐4‐[4‐diethylamino‐1‐methylbutyl] amino quinoline (chloroquine) displays considerable stereoselectivity in its metabolism, pharmacokinetics, macromolecular interactions, and biological activity. The availability of the enantiomers has been hampered

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Absolute configurations have been assigned to the enantiomers of the antimalarial drug quinacrine dihydrochloride. Condensation of ( -)-(R)-4-amino-l-diethylaminopentane (from L-glutamic acid) with 6,9-dichloro-2-methoxyacridine gave ( -)-(R)-6-chloro-9-(4'diethylamino-1'-methylbutyl) amino-2-methox