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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752949Generated: October 28, 2026

Pyridine → 5-Bromo-2-(5-methyl-1,3,4-oxadiazol-2-yl)pyridine

https://huagongshe.com/reaction/1752949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
Reactant5-Bromo-2-(2H-tetrazol-5-yl)pyridineHCID 23438683—
SolventAcetic AnhydrideHCID 7918—
Product5-Bromo-2-(5-methyl-1,3,4-oxadiazol-2-yl)pyridineHCID 2343864380%

Reaction Steps

In 130 ml of acetic anhydride was dissolved 8.6 g of 2-(tetrazol-5-yl)-5-bromopyridine prepared in the Preparation example 6. And then the solution was added with 15 ml of pyridine and stirred for 3 hours for reaction. The reaction mixture was added with ethyl acetate and extracted to separate organic layer. And then the organic layer was washed with water and brine. The organic layer was dehydrated, filtrated and concentrated in vacuo to give 7.3 g of the title compound. Yield 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163043B2
Source datasetuspto-grants-2015_10
ORD IDord-922b978cd7784d899d3e8bca634c9442
Source noteuspto-grants-2015_10