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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887727Generated: November 1, 2026

Potassium Permanganate → 3-Amino-6-chloropyridine-2-carboxylic acid

https://huagongshe.com/reaction/887727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PermanganateHCID 516875—
Reactant6-Chloro-2-(2-furanyl)-3-pyridinamineHCID 59355418—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product3-Amino-6-chloropyridine-2-carboxylic acidHCID 5339343467.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Amino-6-chloro-2-(2-furanyl)pyridine (1.06 g) was dissolved in acetone (25 mL) and cooled in an ice bath to 0° C. A solution prepared of potassium permanganate (2.57 g) in water (40 mL) was added drop wise to this solution. After complete addition, the reaction mixture was allowed to warm to room temperature and stirred for hours. The mixture was cooled again to 0° C. and a second portion of potassium permanganate (858 mg) in water (15 mL) was added and the cool bath removed. After stirring for 2 hours, the reaction mixture was filtered through a pad of celite, the filter cake was washed carefully with water, methanol and ethyl acetate and concentrated to approx. 20 mL on a rotary evaporator. 2N Sodium hydroxide solution was added to adjust the pH-value to −12 and the aqueous layer was washed 2× with MTB-ether. The aqueous layer was adjusted to pH ˜2 by addition of 6N hydrochloric acid and extracted 3× with MTB-ether. The combined organic layer was washed with brine, dried over MgSO4 and concentrated in vacuum to afford 636 mg of the title compound of the formula

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247431B2
Source datasetuspto-grants-2012_08
ORD IDord-77dde900d7224338839c78676b81614b
Source noteuspto-grants-2012_08