Literature DB >> 31571700

Modified synthesis of NOP receptor antagonist SB612111.

David A Perrey1, Jun-Xu Li2, Yanan Zhang1.   

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.

Entities:  

Keywords:  NOP; SB612111; antagonist; modified synthesis

Year:  2016        PMID: 31571700      PMCID: PMC6768550          DOI: 10.1055/s-0036-1588379

Source DB:  PubMed          Journal:  Synthesis (Stuttg)        ISSN: 0039-7881            Impact factor:   3.157


  23 in total

Review 1.  International Union of Pharmacology. XLVI. G protein-coupled receptor list.

Authors:  Steven M Foord; Tom I Bonner; Richard R Neubig; Edward M Rosser; Jean-Phillipe Pin; Anthony P Davenport; Michael Spedding; Anthony J Harmar
Journal:  Pharmacol Rev       Date:  2005-06       Impact factor: 25.468

Review 2.  Pharmacology of nociceptin and its receptor: a novel therapeutic target.

Authors:  G Calo'; R Guerrini; A Rizzi; S Salvadori; D Regoli
Journal:  Br J Pharmacol       Date:  2000-04       Impact factor: 8.739

3.  cDNA cloning and regional distribution of a novel member of the opioid receptor family.

Authors:  K Fukuda; S Kato; K Mori; M Nishi; H Takeshima; N Iwabe; T Miyata; T Houtani; T Sugimoto
Journal:  FEBS Lett       Date:  1994-04-18       Impact factor: 4.124

4.  cDNA cloning of an orphan opiate receptor gene family member and its splice variant.

Authors:  J B Wang; P S Johnson; Y Imai; A M Persico; B A Ozenberger; C M Eppler; G R Uhl
Journal:  FEBS Lett       Date:  1994-07-04       Impact factor: 4.124

5.  Pharmacological profiles of a novel opioid receptor-like1 (ORL(1)) receptor antagonist, JTC-801.

Authors:  Hideki Yamada; Hiromitsu Nakamoto; Yasunori Suzuki; Takao Ito; Kazuo Aisaka
Journal:  Br J Pharmacol       Date:  2002-01       Impact factor: 8.739

Review 6.  The molecular and behavioral pharmacology of the orphanin FQ/nociceptin peptide and receptor family.

Authors:  J S Mogil; G W Pasternak
Journal:  Pharmacol Rev       Date:  2001-09       Impact factor: 25.468

7.  Modification of nociception and morphine tolerance by the selective opiate receptor-like orphan receptor antagonist (-)-cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol (SB-612111).

Authors:  Paola F Zaratin; Giuseppe Petrone; Massimo Sbacchi; Martine Garnier; Claudia Fossati; Paola Petrillo; Silvio Ronzoni; Giuseppe A M Giardina; Mark A Scheideler
Journal:  J Pharmacol Exp Ther       Date:  2003-10-30       Impact factor: 4.030

Review 8.  Nociceptin/Orphanin FQ Receptor Structure, Signaling, Ligands, Functions, and Interactions with Opioid Systems.

Authors:  Lawrence Toll; Michael R Bruchas; Girolamo Calo'; Brian M Cox; Nurulain T Zaveri
Journal:  Pharmacol Rev       Date:  2016-03-08       Impact factor: 25.468

Review 9.  Reverse physiology: discovery of the novel neuropeptide, orphanin FQ/nociceptin.

Authors:  O Civelli; H P Nothacker; R Reinscheid
Journal:  Crit Rev Neurobiol       Date:  1998

10.  Cloning and functional characterization through antisense mapping of a kappa 3-related opioid receptor.

Authors:  Y X Pan; J Cheng; J Xu; G Rossi; E Jacobson; J Ryan-Moro; A I Brooks; G E Dean; K M Standifer; G W Pasternak
Journal:  Mol Pharmacol       Date:  1995-06       Impact factor: 4.436

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.