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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610235Generated: October 31, 2026

Methanol → 2,5-Difluoropyridin-4-amine

https://huagongshe.com/reaction/610235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2,5-Dichloro-3,6-difluoropyridin-4-amineHCID 22121185—
CatalystHCID 178418390HCID 178418390—
SolventTriethylamineHCID 8471—
Product2,5-Difluoropyridin-4-amineHCID 2212117590.8%

Reaction Steps

To 40 ml of methanol were added 4.5 g of 4-amino-2,5-dichloro-3,6-difluoropyridine and 4.5 g of triethylamine together with 0.40 g of 10% palladium carbon, and the mixture was hydrogenated at 50° C. for 12 days. The catalyst was separated by filtration, and the solvent and the like were distilled off under reduced pressure. To the residue was added 100 ml of chloroform, and the mixture was washed with 10 ml of distilled water. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. To the residue were added 1.5 g of triethylamine, 0.35 g of 10% palladium on carbon, and 30 ml of methanol, and the mixture was hydrogenated at 50° C. for 41 hours. The catalyst was separated by filtration, and the solvent and the like were distilled off under reduced pressure. To the residue was added 100 ml of chloroform, and the mixture was washed with 10 ml of distilled water. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 2.67 g of the title compound as precipitate as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998436
Source datasetuspto-grants-1999_12
ORD IDord-21b56d2f74154aacb19c3f78ca1b270f
Source noteuspto-grants-1999_12