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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745448Generated: October 26, 2026

2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester → Methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate

https://huagongshe.com/reaction/745448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl esterHCID 157296—
Reactant4-Methoxy-6-methylpyrimidin-2-amineHCID 587236—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylateHCID 13390184—

Reaction Steps

To 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine in 30 ml of anhydrous acetonitrile was added at ambient temperature, with stirring 3.6 g of 2-methoxycarbonyl-3-thiophenesulfonylisocyanate. The mixture was heated to the boiling point and then allowed to cool to ambient temperature. After stirring for sixteen hours the precipitate present in the mixture was filtered off and washed with anhydrous ethyl ether. The product thus obtained which melted at 165°-173° showed absorption peaks by infrared spectroscopy at 1720 and 1700 cm-1, consistent for the carbonyl groups in the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04599103
Source datasetuspto-grants-1986_07
ORD IDord-845721e64b254fbca5a91e829e3fb36d
Source noteuspto-grants-1986_07