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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789301Generated: October 31, 2026

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

https://huagongshe.com/reaction/1789301

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. 124°-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 numberUS04689072
Source datasetuspto-grants-1987_08
ORD IDord-7122059c556d4c9ca5cb511975cd690a
Source noteuspto-grants-1987_08