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Automated Synthesis of New Quinoxalinetacrines
Author(s) -
BautistaAguilera Óscar M.,
Ismaili Lhassane,
Chioua Mourad,
Iriepa Isabel,
Ángeles MartinezGrau Marìa,
Beadle Christopher D.,
Vetman Tatiana,
LópezMuñoz Francisco,
MarcoContelles José
Publication year - 2020
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.202001593
Subject(s) - tacrine , chemistry , quinoxaline , cholinesterase , butyrylcholinesterase , acetylcholinesterase , combinatorial chemistry , pharmacology , biochemistry , organic chemistry , enzyme , aché , medicine
Tacrine was the first acetylcholinesterase inhibitor approved for the treatment of Alzheimer's disease although its use has been limited and finally abandoned because of side effects including hepatic toxicity. Based on 1,2,3,4‐tetrahydroquinolino[2,3‐ b ]quinoxalin‐12‐amine ( QT78 ), a recently reported cholinesterase inhibitor, less toxic and potent than tacrine as acetylycholinesterase inhibitor, but more selective against butyrylcholinesterase, herein we report the synthesis of novel quinoxalinetacrines QT1‐11 , a series of hybrids designed by juxtaposition of tacrine and quinoxaline. The target compounds have been obtained in moderate yields from 3‐aminoquinoxaline‐2‐carbonitrile and suitable commercially available ketones, under microwave‐promoted Friedländer reactions catalyzed by aluminium trichloride or indium trichloride. These compounds were synthesized remotely in Eli Lilly's Automated Synthesis Laboratory as part of their Open Innovation Drug Discovery program.