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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155632Generated: November 2, 2026

Ethanol → N-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-2-carboxybenzenesulfonamide

https://huagongshe.com/reaction/1155632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
ReactantN-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamideHCID 10810737—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductN-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-2-carboxybenzenesulfonamideHCID 13097297100.6%

Reaction Steps

A mixture containing 5 g of N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamide, 20 ml of ethanol, 2.5 ml of water and 2.5 g of potassium hydroxide was stirred at ambient temperature and pressure for 18 hours. The mixture was then diluted with 250 ml of water and 20 ml of concentrated hydrochloric acid was added with stirring. The precipitate was filtered and washed with water and dried to yield 4.85 g of the desired product, melting at 161°-2° C. The infrared absorption peaks at 3500, 3400 and 1700 cm-1 are consistent with the desired structure and the nuclear magnetic resonance absorption peaks at 3.95 ppm, S, 6H, OCH3 of pyrimidine; 5.8 ppm S, 1H, pyrimidine proton at position 5; and 7.6-8.3 ppm, M, 4H, aromatic protons, are consistent with the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04332611
Source datasetuspto-grants-1982_06
ORD IDord-2620798b91114b5e8510726582e5ec4d
Source noteuspto-grants-1982_06