Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748600Generated: October 30, 2026

Potassium Iodide → HCID 86692553, compound

https://huagongshe.com/reaction/1748600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 86692551HCID 86692551—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductHCID 86692553HCID 8669255381.3%

Reaction Steps

1-(5-Amino-4-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl ester (1.0 g) was suspended in 20% (v/v) sulfuric acid aqueous solution (75 ml), sodium nitrite (318 mg) was added thereto little by little under ice-cooling with stirring, and then stirred for 40 minutes under ice-cooling. Then, potassium iodide (1.27 g) was dissolved in water (12 ml), and the obtained aqueous solution was slowly added dropwise to the reaction solution under ice-cooling with stirring. After the completion of adding dropwise, the solution was stirred for 3 hours under ice-cooling, and then gradually warmed to room temperature. The reaction solution was poured into 10% sodium carbonate aqueous solution, the precipitated solid was collected by filtration, and dissolved in ethyl acetate. The organic layer was sequentially washed with sodium thiosulfate aqueous solution, water, and saturated brine, dried over anhydrous sodium sulfate, and then the solvent was evaporated to give 1-(5-iodo-4-methylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxylic acid ethyl ester (1.16 g) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-23b31b0337c64372b78852a5f264b843
Source noteuspto-grants-2015_10