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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964718Generated: November 1, 2026

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

https://huagongshe.com/reaction/1964718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5-fluoropyridine-2-carboxylic AcidHCID 2762876—
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 numberUS08415359B2
Source datasetuspto-grants-2013_04
ORD IDord-e9099bce0c9744fe89c5a98143382cb0
Source noteuspto-grants-2013_04