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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702529Generated: October 31, 2026

Potassium Carbonate → Methyl 2-[[(4,6-dichloropyrimidin-2-yl)aminocarbonyl]aminosulfonyl]benzeneacetate

https://huagongshe.com/reaction/1702529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4,6-Dichloro-2-isocyanatopyrimidineHCID 12364650—
ReactantMethyl 2-(2-sulfamoylphenyl)acetateHCID 13064551—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-[[(4,6-dichloropyrimidin-2-yl)aminocarbonyl]aminosulfonyl]benzeneacetateHCID 1306455945.3%

Reaction Steps

To 2.3 g of 2-(aminosulfonyl)benzeneacetic acid methyl ester in 30 ml of acetonitrile was added 1.5 g of anhydrous potassium carbonate and 1.6 g of 4,6-dichloropyrimidin-2-yl isocyanate. The mixture was stirred at room temperature for 6 hours, diluted with 250 g of water and acidified to a pH of about 4. The resulting solid was filtered and dried to yield 1.6 g of methyl 2-[[(4,6-dichloropyrimidin-2-yl)aminocarbonyl]aminosulfonyl]benzeneacetate, a pale yellow solid, m.p. 115°-118° C. It showed infrared absorption peaks at 1730, 1600 and 1560 cm-1 and nuclear magnetic resonance peaks at 3.7 ppm, methyl ester group; 4.2 ppm, benzeneacetic group; 6.9 ppm, pyrimidin H; 7.4-7.6 ppm, aromatic hydrogens; consistent for the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348219
Source datasetuspto-grants-1982_09
ORD IDord-1f4837e7f0c047f7a0f457b13ae46a87
Source noteuspto-grants-1982_09