41959-29-9

Usage

Uses

Used in Pharmaceutical Industry:
2-Benzyl-6-hydroxy-2-azabicyclo[2.2.2]octane is used as a pharmaceutical compound for its potential medicinal properties. Its unique structure and functional groups may contribute to the development of new drugs or the enhancement of existing ones, offering novel therapeutic options.
Used in Chemical Industry:
In the chemical industry, 2-Benzyl-6-hydroxy-2-azabicyclo[2.2.2]octane is used as a chemical intermediate for the synthesis of various organic compounds. Its benzyl and hydroxyl functional groups can be utilized in chemical reactions to produce a range of products, contributing to the advancement of chemical research and development.

Upstream product

• 79-37-8 oxalyl dichloride 
• 74403-57-9 2-benzyl-2-aza-bicyclo[2.2.2]octan-3-one 
• 67-68-5 dimethyl sulfoxide 
• 10028-34-9 2-benzyl-2-aza-bicyclo[2.2.2]octane-3,6-dione 
• 41088-52-2 methyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate 
• 100-46-9 benzylamine 
• 38025-71-7 2-benzyl-6-hydroxy-2-aza-bicyclo[2.2.2]octan-3-one 

Relevant academic research and scientific papers

Certain 1-azabicyclo[2.2.1]heptanes useful as muscarinic receptor antagonists

MUSCARINIC RECEPTOR ANTAGONISTS OF THE FOLLOWING FORMULAE: STR1 Muscarinic receptor antagonists, useful especially in the treatment of irritable bowel syndrome, of formula (IA) or (IB) or a pharmaceutically acceptable salt thereof, where R 2 and R 3 are each independently H, halo or C 1 -C 4 alkyl; m is 0, 1 or 2; n is 1, 2 or 3; Y is a direct link, O or S; with the proviso that when n is 1, Y is a direct link; Het is a group of formula (A) or (B), where p is 0, 1 or 2, q is 1, 2 or 3, and r is 0, 1, 2 or 3, with the proviso that the sum of p, q and r is at least 3, the N atom of ""Het"" being attached to the group (CH 2) n in formula (IA) and to the H atom in formula (IB); and R 1 is a group of formula (a), (b) or Het 1, where R 4 and R 5 are each independently H, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, --(CH 2) t OH, halo, trifluoromethyl, cyano, --(CH 2) t NR 6 R 7, --CO(C 1 -C 4 alkyl), --OCO(C 1 -C 4 alkyl), CH(OH)(C 1 -C 4 alkyl), --C(OH)(C 1 -C 4 alkyl) 2, --SO 2 NH 2, --(CH 2) t CONR 6 R 7 or --(CH 2) t COO(C 1 -C 4 alkyl); R 6 and R 7 are each independently H or C 1 -C 4 alkyl; t is 0, 1 or 2; X and X 1 are each independently O or CH 2 ; s is 1, 2 or 3; and Het 1 is pyridyl, pyrazinyl or thienyl.

5-(1,1-Diphenyl-3-(5- or 6-hydroxy-2-azabicyclo(2.2.2)oct-2-yl)propyl)-2-alkyl-1,3,4-oxadiazoles and related compounds

This invention encompasses novel 5-[1,1-diphenyl-3-(5-or 6-hydroxy-2-azabicyclo[2.2.2]oct-2-yl)propyl]-2-alkyl-1,3,4-oxadiazoles and their lower O-alkanoyl derivatives. These compounds are useful anti-diarrheal agents and also possess little or no analges