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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120106Generated: October 30, 2026

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

https://huagongshe.com/reaction/2120106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant5-Bromo-2-(2H-tetrazol-5-yl)pyridineHCID 23438683—
Product5-Bromo-2-(5-methyl-1,3,4-oxadiazol-2-yl)pyridineHCID 23438643—

Reaction Steps

In 10 ml of acetic anhydride was dissolved 1 g of 2-(5-tetrazolyl)-5-bromopyridine, followed by refluxing for 2 hours. After completion of the reaction, the same post-treatment as in Preparation Example 13 was conducted to give the title compound. 0.6 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689779B2
Source datasetuspto-grants-2004_02
ORD IDord-bae44cf0b4384f059428f5c6467c2335
Source noteuspto-grants-2004_02