Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059663Generated: November 1, 2026

Acetic Acid → 2-Chloro-6-methyl-4-(5-methyl-[1,2,4]oxadiazol-3-yl)-pyridine

https://huagongshe.com/reaction/2059663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 178426669HCID 178426669—
SolventTrimethylorthoacetateHCID 21927715—
Product2-Chloro-6-methyl-4-(5-methyl-[1,2,4]oxadiazol-3-yl)-pyridineHCID 59534443—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Chloro-N-hydroxy-6-methyl-isonicotinamidine (120 mg) was suspended in trimethylorthoacetate (3 ml) under inert atmosphere and acetic acid (0.3 ml) was added. The mixture was heated to 100° C. and stirred for 2 h. After cooling to room temperature the solvent was evaporated under reduced pressure and the residue partitioned between EtOAc and aqueous solution of NaHCO3. The organic layer was separated, washed with water and brine, dried under Na2SO4, filtered and the solvent was evaporated under reduced pressure. The crude was purified by flash column chromatography (10 g Isolute® silica gel cartridge; gradient elution: hexane/EtOAc from 10/0 to 9/1) affording the title compound (107 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278302B2
Source datasetuspto-grants-2012_10
ORD IDord-a3f386dfd32f4497a39099a5a1eed0ca
Source noteuspto-grants-2012_10