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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463975Generated: October 27, 2026

Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester → Methyl 2-[(4-methoxy-6-methyl-pyrimidin-2-yl)carbamoylsulfamoyl]benzoate

https://huagongshe.com/reaction/463975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid, 2-(isocyanatosulfonyl)-, methyl esterHCID 156281—
Reactant4-Methoxy-6-methylpyrimidin-2-amineHCID 587236—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-[(4-methoxy-6-methyl-pyrimidin-2-yl)carbamoylsulfamoyl]benzoateHCID 1317657821.1%

Reaction Steps

To a stirred suspension of 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine in 30 ml of anhydrous methylene chloride was added at ambient temperature 2.4 g of 2-methoxycarbonylbenzenesulfonylisocyanate. After stirring for 16 hours, the foregoing mixture was filtered to remove unreacted amine, and the filtrate evaporated at temperatures up to 40° and reduced pressure. The resultant residue was stirred in 25 ml of water, the pH adjusted to 10 by the addition of 50% sodium hydroxide and the solution filtered. Acidification of the filtrate to pH 3 with hydrochloric acid caused precipitation of the desired product which was removed by filtration and dried to yield 0.8 g of product melting at 173°-179°. It showed infrared absorption peaks at 1720, 1680, 1630 and 1550 cm-1, consistent for N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04545808
Source datasetuspto-grants-1985_10
ORD IDord-e31e84383a91465b8e71ed659ea11ff6
Source noteuspto-grants-1985_10