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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966927Generated: November 1, 2026

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

https://huagongshe.com/reaction/1966927

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 numberUS08420676B2
Source datasetuspto-grants-2013_04
ORD IDord-1f860b6a2256411b9fb06dc1a284974e
Source noteuspto-grants-2013_04