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An efficient multigram synthesis of the potent histamine H3 antagonist GT-2331 and the reassessment of the absolute configuration.
Liu, Huaqing; Kerdesky, Francis A; Black, Lawrence A; Fitzgerald, Michael; Henry, Rodger; Esbenshade, Timothy A; Hancock, Arthur A; Bennani, Youssef L.
Affiliation
  • Liu H; Neuroscience Research, Global Pharmaceutical Research Division, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, Illinois 60064-6123, USA. huaqing.liu@abbott.com
J Org Chem ; 69(1): 192-4, 2004 Jan 09.
Article in En | MEDLINE | ID: mdl-14703397
GT-2331 is a potent histamine H(3) antagonist which has entered clinical trials. Efficient multigram syntheses of this compound and its enantiomer are described. The literature reports that GT-2331 is the dextrorotatory (+), more potent, enantiomer of 4-[2-(5,5-dimethylhex-1-ynyl)cyclopropyl]-1H-imidazole with the absolute configuration of (1R,2R)-1. However, we found that the dextrorotatory, more potent, enantiomer of 4-[2-(5,5-dimethylhex-1-ynyl)cyclopropyl]-1H-imidazole has the (1S,2S) absolute configuration. We suggest a reconsideration of the absolute configuration of GT-2331.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Histamine H3 / Histamine Agents / Imidazoles Language: En Journal: J Org Chem Year: 2004 Document type: Article Affiliation country: United States Country of publication: United States
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Histamine H3 / Histamine Agents / Imidazoles Language: En Journal: J Org Chem Year: 2004 Document type: Article Affiliation country: United States Country of publication: United States