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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207619Generated: November 1, 2026

Hydrochloric Acid → Methyl 4-(5-ethoxy-2-fluoro-phenyl)-5,6-dimethyl-pyridine-2-carboxylate

https://huagongshe.com/reaction/2207619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant1,4-DioxaneHCID 31275—
Reactant4-(5-Ethoxy-2-fluoro-phenyl)-5,6-dimethyl-pyridine-2-carbonitrileHCID 89649590—
ProductMethyl 4-(5-ethoxy-2-fluoro-phenyl)-5,6-dimethyl-pyridine-2-carboxylateHCID 89649357—

Reaction Steps

4M HCl in 1,4-dioxan (20 mL, 80 mmol) was added to a suspension of 4-(5-ethoxy-2-fluoro-phenyl)-5,6-dimethyl-pyridine-2-carbonitrile (which may be prepared as described in Description 51) (1.87 g, 6.92 mmol) in methanol (20 mL) at ambient temperature. The stirred, yellow solution was refluxed under N2 for 9 h. The reaction was concentrated to one third the volume then poured into sat. aq. NaHCO3 (100 ml). The mixture was extracted with EtOAc (3×50 ml). The combined organic extracts were dried (Na2SO4) and evaporated to a colourless oil which solidified. This was purified by SiO2 column chromatography: the oil was dissolved in DCM (15 ml) and the solution was applied to a 100 g cartridge which was then eluted on a Biotage SP4 system with a gradient of EtOAc/iso-hexane (0-80%) to afford methyl 4-(5-ethoxy-2-fluoro-phenyl)-5,6-dimethyl-pyridine-2-carboxylate (D52);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376436B2
Source datasetuspto-grants-2016_06
ORD IDord-8aabdd4bc27842679408c555d364774c
Source noteuspto-grants-2016_06