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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074966Generated: October 26, 2026

2,6-Dimethyl-4-aminopyrimidine → N-[(2,6-dimethylpyrimidin-4-yl)aminocarbonyl]2-methoxycarbonylbenzenesulfonamide

https://huagongshe.com/reaction/1074966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dimethyl-4-aminopyrimidineHCID 68039—
ReactantBenzoic acid, 2-(isocyanatosulfonyl)-, methyl esterHCID 156281—
SolventAcetonitrileHCID 6342—
ProductN-[(2,6-dimethylpyrimidin-4-yl)aminocarbonyl]2-methoxycarbonylbenzenesulfonamideHCID 13176760—

Reaction Steps

To a suspension of 1.2 g of 4-amino-2,6-dimethylpyrimidine in 30 ml of dry acetonitrile with stirring was added 2.4 g of 2-methoxycarbonylbenzenesulfonylisocyanate. The mixture was stirred for two hours at ambient temperature, allowed to stand for sixteen hours and the desired product, which had precipitated, was removed by filtration and washed with butyl chloride to yield 2.4 g, m.p. 125°-127°. The product showed absorption peaks by Nuclear Magnetic Resource at 4.0, 2.62 and 2.9 ppm; consistent for the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04394506
Source datasetuspto-grants-1983_07
ORD IDord-11c10d0a954c40588c83983673205a7e
Source noteuspto-grants-1983_07