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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633698Generated: October 25, 2026

Pyridine → N-methoxy-N,3,5-trimethylisoxazole-4-carboxamide

https://huagongshe.com/reaction/633698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant3,5-Dimethylisoxazole-4-carbonyl ChlorideHCID 2736265—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductN-methoxy-N,3,5-trimethylisoxazole-4-carboxamideHCID 5110975398.9%

Reaction Steps

659 μl (8.15 mmol) of pyridine are added to a suspension of 343.07 mg (3.45 mmol) of N,O-dimethylhydroxylamine hydrochloride in 10 mL of dichloromethane. The mixture is stirred at room temperature until fully dissolved. A solution of 526.32 mg (3.13 mmol) of 3,5-dimethylisoxazole-4-carbonyl chloride in 5 mL of dichloromethane is then added. After stirring for 1 hour at room temperature, the reaction mixture is taken up in saturated aqueous NaHCO3 solution and stirred for a few minutes, and the phases are separated by settling. The organic phase is dried over magnesium sulfate and evaporated to dryness. The residue obtained is taken up in toluene and evaporated, the operation being repeated a second time. 570 mg of N-methoxy-N-methyl-3,5-dimethylisoxazole-4-carboxamide are then obtained, corresponding to the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321790B2
Source datasetuspto-grants-2016_04
ORD IDord-31d42ef2e01f42079414ff88fdf1d682
Source noteuspto-grants-2016_04