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Updated: Jan 6, 2026

Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates
Published on: March 6, 2019
Modified synthesis of NOP receptor antagonist SB612111
David A Perrey1, Jun-Xu Li2, Yanan Zhang1
1Research Triangle Institute, Research Triangle Park, North Carolina 27709, USA.
Abstract:
SB612111 ((5S,7S)-7-{[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl}-1-methyl-6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-ol) is a potent and selective antagonist of the nociception/orphanin FQ peptide (NOP) receptor. In the process of synthesizing cis-SB612111 to support ongoing animal studies, several key steps of the published syntheses in the patent literature proceeded in low yields in our hands, particularly with the route to the key intermediate piperidine 3, the reduction of amide 14, lactone 17 formation and the final reductive amination between 18 and 3 in the diastereoselective synthesis. We have thus explored various reaction conditions and successfully improved the yields for the necessary synthetic steps. We herein report our modified synthesis of SB612111 as the cis-diastereomers.
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