An efficient multigram synthesis of the potent histamine H3 antagonist GT-2331 and the reassessment of the absolute configuration.
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.
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