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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280442Generated: October 29, 2026

Hydrochloric Acid → N-(4-azidophenylsulfonyl)-N'-(4-methoxy-6-methylpyrimidin-2-yl)urea

https://huagongshe.com/reaction/280442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,5-Diazabicyclo(5,4,0)undec-5-eneHCID 314112—
Reactant4-AzidobenzenesulfonamideHCID 3558590—
ReactantN-(4-methoxy-6-methylpyrimidin-2-yl)phenylcarbamateHCID 18954641—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-azidophenylsulfonyl)-N'-(4-methoxy-6-methylpyrimidin-2-yl)ureaHCID 2332046267%

Reaction Steps

A solution of 2.9 g of N-(4-methoxy-6-methylpyrimidin-2-yl)phenylcarbamate in 10 ml of dioxan is added dropwise at 20°-25° C. to a solution of 2 g of 4-azidophenylsulfonamide and 1.6 ml of 1,5-diazabicyclo(5,4,0)-undec-5-ene in 20 ml of dioxan and the mixture is stirred for 3 hours at the same temperature. The reaction mixture is then taken up in 200 ml of water and the aqueous mixture is then acidified with hydrochloric acid to pH 2. The precipitated product is isolated, washed with ethyl acetate and dried, affording N-(4-azidophenylsulfonyl)-N'-(4-methoxy-6-methylpyrimidin-2-yl)urea in 67% yield in the form of greenish crystals with a melting point of 192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04589912
Source datasetuspto-grants-1986_05
ORD IDord-f5cd7d39e6fb45bea731dea7ea0ea439
Source noteuspto-grants-1986_05