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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188902Generated: October 29, 2026

Potassium Hydroxide → 6-Bromo-5-chloropyridin-2-amine

https://huagongshe.com/reaction/2188902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 6-bromo-5-chloropyridin-2-ylcarbamateHCID 59165912—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6-Bromo-5-chloropyridin-2-amineHCID 5340119382.3%

Reaction Steps

To a solution of methyl 6-bromo-5-chloropyridin-2-ylcarbamate (1.1 g, 4.1 mmol) in methanol (50 mL) was added KOH (700 mg, 13 mmol) at room temperature. The mixture was heated at reflux for 2 hr. The reaction mixture was diluted with water and extracted with ethyl acetate (20 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under vacuum. The residue was purified by column chromatography on silica gel (5% to 10% EtOAc in petroleum ether) to give 6-bromo-5-chloropyridin-2-amine (700 mg, 81%). 1H NMR (400 MHz, CDCl3) 7.54 (d, J=8.0 Hz, 1H), 6.41 (d, J=8.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324207B2
Source datasetuspto-grants-2012_12
ORD IDord-63d567c6219841d8a791c6e01f30a651
Source noteuspto-grants-2012_12