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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280803Generated: October 29, 2026

Dichloromethane → N-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamide

https://huagongshe.com/reaction/280803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-4,6-dimethoxypyrimidineHCID 118946—
ReactantBenzoic acid, 2-(isocyanatosulfonyl)-, methyl esterHCID 156281—
SolventWaterHCID 962—
ProductN-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamideHCID 1081073743.1%

Reaction Steps

A mixture containing 1.6 g of 2-amino-4,6-dimethoxypyrimidine, 30 ml of anhydrous methylene chloride and 2.4 g of 2-methoxycarbonylbenzenesulfonylisocyanate was stirred at ambient temperature and pressure for 16 hours. It was then filtered to remove unreacted amine and the filtrate evaporated at temperatures up to 40° and reduced pressure. The residue thus obtained was stirred in 25 ml of water, the pH adjusted to 10 by the addition of 50% aqueous sodium hydroxide and the solution filtered. Acidification of the filtrate to pH 3 caused the formation of a precipitate. Filtration and drying the precipitate yielded 1.7 g of the desired product, melting at 185°-190°. Its infrared absorption peaks at 1700 and 1710 cm-1 are consistent for the desired structure and the nuclear magnetic resonance absorption peaks at 3.8 and 3.85 are consistent for the two different types of methoxy groups brought together in this product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04591378
Source datasetuspto-grants-1986_05
ORD IDord-ab65e4b8033944288b22a086138b80e7
Source noteuspto-grants-1986_05