Synthesis and characterization of chiral 6-azaspiro[2.5]octanes as potent and selective antagonists of the M muscarinic acetylcholine receptor

Authors

Bender AM Aaron M , Carter TR Trever R , Spock M Matthew , Rodriguez AL Alice L , Dickerson JW Jonathan W , Rook JM Jerri M , Chang S Sichen , Qi A Aidong , Presley CC Christopher C , Engers DW Darren W , Harp JM Joel M , Bridges TM Thomas M , Niswender CM Colleen M , Conn PJ P Jeffrey , Lindsley CW Craig W .
Bioorganic & medicinal chemistry letters. 2021 11 24; 56().
128479

PMID: 34838649

Abstract

In this manuscript, we report a series of chiral 6-azaspiro[2.5]octanes and related spirocycles as highly potent and selective antagonists of the muscarinic acetylcholine receptor subtype 4 (mAChR). Chiral separation and subsequent X-ray crystallographic analysis of early generation analogs revealed the R enantiomer to possess excellent human and rat M potency, and further structure-activity relationship (SAR) studies on this chiral scaffold led to the discovery of VU6015241 (compound 19). Compound 19 is characterized by high M potency and selectivity across multiple species, excellent aqueous solubility, and moderate brain exposure in rodents after intraperitoneal administration.