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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905614Generated: November 1, 2026

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

https://huagongshe.com/reaction/1905614

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 numberUS04647303
Source datasetuspto-grants-1987_03
ORD IDord-012dce7c670c4eb3b169bf0e358bcbf2
Source noteuspto-grants-1987_03