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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909662Generated: November 3, 2026

Triethylamine → 5-fluoro-N-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/909662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5-fluoropyridine-2-carboxylic AcidHCID 2762876—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantMonomethylamine methanolHCID 57454252—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-fluoro-N-methylpyridine-2-carboxamideHCID 6668339491%

Reaction Steps

5-Fluoropyridine-2-carboxylic acid (495 mg, 3.51 mmol) was dissolved in methylene chloride (10 mL), and HOBt•H2O (591 mg, 3.86 mmol), WSCI•HCl (1.35 g, 7.02 mmol), triethylamine (2.44 mL, 17.5 mmol) and 40% methylamine/methanol solution (0.82 mL, 10.5 mmol) were added, followed by stirring for 15 hours. To the reaction solution, water (30 mL) was added, and extraction was carried out twice with methylene chloride (30 mL). The organic layer was washed with saturated brine, and subsequently dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified using silica gel column chromatography (elution solvent: ethyl acetate/hexane=0%-50%) to afford the desired compound (490 mg, yield 91%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017610B2
Source datasetuspto-grants-2011_09
ORD IDord-8bd557ac5aa240f0a6c1b28f8ddb6b72
Source noteuspto-grants-2011_09