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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715916Generated: October 30, 2026

Ethyl Acetate → 2,5-Difluoro-N-methoxy-N-methylnicotinamide

https://huagongshe.com/reaction/715916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2,5-difluoropyridine-3-carboxylic AcidHCID 11815999—
Catalyst1-HydroxybenzotriazoleHCID 75771—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDiisopropylethylamineHCID 81531—
Product2,5-Difluoro-N-methoxy-N-methylnicotinamideHCID 9161896463.5%

Reaction Steps

To a solution of 2,5-difluoropyridine-3-carboxylic acid (3.00 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (4.34 g), 1-hydroxybenzotriazole (127 mg), and N,O-dimethylhydroxylamine hydrochloride (1.93 g) in N,N-dimethylformamide (30 ml), diisopropylethylamine (7.42 ml) was added, and the mixture was stirred overnight at room temperature. Ethyl acetate and water were added to the reaction solution to separate the aqueous and organic layers. The aqueous layer was subjected to extraction with ethyl acetate. The organic layers were combined, washed with saturated saline, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain the title compound (2.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187489B2
Source datasetuspto-grants-2015_11
ORD IDord-264b2750b84c4af2b44b8bbf3e1a064d
Source noteuspto-grants-2015_11