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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068691Generated: November 2, 2026

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

https://huagongshe.com/reaction/2068691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 136397847HCID 136397847—
SolventAcetic AcidHCID 176—
Product5-Bromo-2-(5-methyl-1,2,4-oxadiazol-3-yl)pyridineHCID 2343861045%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-bromo-N′-hydroxypicolinimidamide II (0.75 g, 3.50 mmol) in acetic acid (50.0 mL) was added acetic anhydride (0.75 mL, 7.0 mmol) and the resulting reaction mixture was heated to 100° C. for 2 h. After the completion of reaction (TLC monitoring), acetic acid was distilled off, added water (25.0 mL) and extracted with EtOAc (2×50 mL). The combined organics was washed with brine, dried (Na2SO4), filtered and concentrated to obtain the desired product (0.27 g, 45%). MS: 240.01 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299065B2
Source datasetuspto-grants-2012_10
ORD IDord-0faa30e588764b6fad944d8e1a0bb74f
Source noteuspto-grants-2012_10