Exploration of piperidine 3D fragment chemical space: synthesis and 3D shape analysis of fragments derived from 20 regio- and diastereoisomers of methyl substituted pipecolinates. Issue 12 (28th October 2022)

• Record Type: Journal Article
• Authors: Jones, S. Paul; Firth, James D.; Wheldon, Mary C.; Atobe, Masakazu; Hubbard, Roderick E.; Blakemore, David C.; De Fusco, Claudia; Lucas, Simon C. C.; Roughley, Stephen D.; Vidler, Lewis R.; Whatton, Maria Ann; Woolford, Alison J.-A.; Wrigley, Gail L.; O'Brien, Peter
• Is Part Of: RSC medicinal chemistry. Volume 13:Issue 12(2022)
• Page Start: 1614
• Page End: 1620
• Publication Date: 2022-10-28
• Subjects: Pharmaceutical chemistry -- Periodicals; 615.19005
• DOI: 10.1039/d2md00239f
• Languages: English
• ISSNs: 2632-8682

Abstract

Abstract : The synthesis and 3D shape analysis of fragments derived from 20 regio- and diastereoisomers of methyl substituted pipecolinates is described. Abstract : Fragment-based drug discovery is now widely adopted for lead generation in the pharmaceutical industry. However, fragment screening collections are often predominantly populated with flat, 2D molecules. Herein, we report the synthesis of piperidine-based 3D fragment building blocks – 20 regio- and diastereoisomers of methyl substituted pipecolinates using simple and general synthetic methods. cis -Piperidines, accessed through a pyridine hydrogenation were transformed into their trans -diastereoisomers using conformational control and unified reaction conditions. Additionally, diastereoselective lithiation/trapping was utilised to access trans -piperidines. Analysis of a virtual library of fragments derived from the 20 cis - and trans -disubstituted piperidines showed that it consisted of 3D molecules with suitable molecular properties to be used in fragment-based drug discovery programs.