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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422414Generated: October 31, 2026

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

https://huagongshe.com/reaction/1422414

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 numberUSRE045323E1
Source datasetuspto-grants-2015_01
ORD IDord-0e6cea59468a4e678ea582219a2287f7
Source noteuspto-grants-2015_01