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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650079Generated: October 26, 2026

Hydrochloric Acid → 2-[(4,6-Dimethoxypyrimidin-2-yl)thio]-6-methylbenzoic acid

https://huagongshe.com/reaction/1650079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4,6-Dimethoxy-2-(methylsulfonyl)pyrimidineHCID 838363—
Reactant2-Mercapto-6-methylbenzoic acidHCID 12612809—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[(4,6-Dimethoxypyrimidin-2-yl)thio]-6-methylbenzoic acidHCID 338689012.2%

Reaction Conditions

Temperature115 °C

Reaction Steps

Then, 3.6 g of 2-mercapto-6-methylbenzoic acid, 4.7 g of 4,6-dimethoxy-2-methylsulfonylpyrimidine and 3.5 g of unhydrous potassium carbonate were dissolved in 20 ml of dimethylformamide, and then the mixture was stirred at from 110 to 120° C. for one hour. The reaction solution was poured into a large amount of water, and concentrated hydrochloric acid was added thereto. Then, the mixture was extracted with chloroform. The chloroform layer was washed with water and dried, and then the solvent was distilled off under reduced pressure. The crude crystals were purified by column chromatography by using a developing solvent of hexane/ethyl acetate and recrystallized from ethyl acetate to obtain 0.8 g of 2-[(4,6-dimethoxypyrimidin-2-yl)thio]-6-methylbenzoic acid as white powder. Melting point: 131°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923501
Source datasetuspto-grants-1990_05
ORD IDord-f4abf0cb65524ae692f2e69e60bbc2ba
Source noteuspto-grants-1990_05