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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748444Generated: October 31, 2026

Sulfuric Acid → 1-(5-Iodo-6-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1748444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant1-(5-amino-6-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl esterHCID 86692412—
SolventWaterHCID 962—
Product1-(5-Iodo-6-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl esterHCID 8669241469.8%

Reaction Steps

After concentrated sulfuric acid (20 ml) were added to 1-(5-amino-6-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl ester (7.8 g) and water (80 ml) at 0° C., sodium nitrite (3.0 g) was added therein in several portions. After stirring for 0.5 hour, potassium iodide (9.96 g) was added in several portions and the mixture was stirred for 2.5 hours at room temperature. A saturated aqueous solution of sodium bicarbonate was added in several portions at 0° C. and then an aqueous solution of sodium sulfite was added and the aqueous solution was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting solid was washed with ethyl acetate and n-hexane to give the titled compound (7.76 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-0df563de4d2c4e5faf7d28af19e17545
Source noteuspto-grants-2015_10