Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762049Generated: October 29, 2026

2-Aminopyrimidine → Methyl 2-[[[(2-pyrimidinylamino)carbonyl]amino]sulfonyl]benzoate

https://huagongshe.com/reaction/1762049

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyrimidineHCID 7978—
ReactantBenzoic acid, 2-(isocyanatosulfonyl)-, methyl esterHCID 156281—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-[[[(2-pyrimidinylamino)carbonyl]amino]sulfonyl]benzoateHCID 1317657965.7%

Reaction Steps

With stirring at ambient temperature, 1.0 g of 2-aminopyrimidine in 25 ml of anhydrous acetonitrile was added to 2.4 g of 2-methoxycarbonylbenzenesulfonylisocyanate. After stirring that mixture for 24 hours, the resultant precipitate was filtered off to yield 2.2 g of the desired compound which melted at 188°-192°. Its showing infrared absorption peaks at 1700, 1680 and 1580 cm-1 is consistent for N-[(pyrimidin-2-yl)aminocarbonyl)-2-methoxycarbonylbenzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04830662
Source datasetuspto-grants-1989_05
ORD IDord-15f7bfd5bb0e435cafe9bbf794a2eb8b
Source noteuspto-grants-1989_05