Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274710Generated: November 2, 2026

Methanol → 2-(t-Butylamino)-5-chloro-3,6-difluoropyridine

https://huagongshe.com/reaction/1274710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-Bromo-2-(t-butylamino)-5-chloro-3,6-difluoropyridineHCID 22121170—
CatalystPalladiumHCID 23938—
SolventTriethylamineHCID 8471—
Product2-(t-Butylamino)-5-chloro-3,6-difluoropyridineHCID 2212118998.6%

Reaction Steps

To 30 ml of methanol were added 12.8 g of 4-bromo-2-(t-butylamino)-5-chloro-3,6-difluoropyridine and 2.5 g of triethylamine together with 0.57 g of 10% palladium on carbon, and the mixture was hydrogenated at 50° C. for 5 days. The catalyst was separated by filtration, and the solvent and the like were distilled off under reduced pressure. To the residue was added 80 ml of chloroform, and the mixture was washed with 70 ml of distilled water, and the chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 9.3 g of the title compound as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156903
Source datasetuspto-grants-2000_12
ORD IDord-cd5aa83f6ff24021a774203de67e4f55
Source noteuspto-grants-2000_12