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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366078Generated: October 31, 2026

Pivaloyl chloride → 5-(5-Tert-butyl-1,2,4-oxadiazol-3-yl)-2-chloropyridine

https://huagongshe.com/reaction/2366078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
Reactant6-Chloro-N-hydroxy-nicotinamidineHCID 33678499—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
Product5-(5-Tert-butyl-1,2,4-oxadiazol-3-yl)-2-chloropyridineHCID 8665995721%

Reaction Steps

A mixture of 1.5 g (8.74 mmol) of 6-chloro-N′-hydroxypyridine-3-carboximidamide and 1.13 mL (9.18 mmol) of trimethylacetyl chloride in 15 mL of toluene is stirred for 1 hour at room temperature and then refluxed for 4 hours. The medium is filtered. The insoluble material formed is dissolved in 15 mL of AcOH and then heated at 60° C. for 5 hours. After cooling to room temperature, the medium is concentrated under reduced pressure and then purified by chromatography on silica gel, eluting with a cyclohexane/EtOAc mixture (9/1). 0.39 g of 5-(5-tert-butyl-1,2,4-oxadiazol-3-yl)-2-chloropyridine is obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697731B2
Source datasetuspto-grants-2014_04
ORD IDord-acee6a1dd39d4661b5de728e31514b8e
Source noteuspto-grants-2014_04