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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878672Generated: November 1, 2026

4-Aminopyridine → HCID 62235240, compound

https://huagongshe.com/reaction/1878672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant6-Chloropicolinic acidHCID 20812—
SolventThionyl ChlorideHCID 24386—
ProductHCID 62235240HCID 62235240—

Reaction Conditions

Temperature25 °C

Reaction Steps

6-Chloropicolinic acid (0.50 g, 3.17 mmol) was dissolved in thionyl chloride (5.0 mL) and stirred at 25° C. for 1 hour. The thionyl chloride was evaporated, and 4-aminopyridine (0.28 g, 2.98 mmol), triethylamine (0.415 mL, 2.98 mmol) and dichloromethane (50 mL) were added. The solution was stirred at 25° C. for 18 hours. The reaction mixture was partitioned between dichloromethane (50 mL) and saturated sodium bicarbonate solution (100 mL). The organic layer was dried (sodium sulfate) and concentrated, and the residue was purified by silica gel flash column chromatography to afford the titled compound: 1H NMR (500 MHz, methanol-D4) δ ppm 7.71 (dd, J=7.9, 0.9 Hz, 1H), 7.91-7.95 (m, 2H), 8.05 (t, J=7.8 Hz, 1), 8.20 (dd, J=7.6, 0.6 Hz, 1H), 8.43-8.52 (m, 2H) MS (ESI) m/z=335 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314119B2
Source datasetuspto-grants-2012_11
ORD IDord-3ba068f4c404419790d2dece89210e49
Source noteuspto-grants-2012_11