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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279735Generated: October 27, 2026

4-Methoxy-6-methylpyrimidin-2-amine → N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methylpyrimidin-2-yl)urea

https://huagongshe.com/reaction/279735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-6-methylpyrimidin-2-amineHCID 587236—
Reactant2-BiphenylylsulfonylisocyanateHCID 13103320—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductN-2-biphenylylsulfonyl-N'-(4-methoxy-6-methylpyrimidin-2-yl)ureaHCID 1310332186.9%

Reaction Steps

13.9 g of 2-amino-4-methoxy-6-methylpyrimidine were dissolved in 150 ml of dry dichloromethane. To this solution was added dropwise a solution of 28.5 g of 2-biphenylylsulfonyl isocyanate in 40 ml of toluene over an hour. During this addition, the internal temperature was maintained at room temperature. When the addition was finished, the mixture was stirred at room temperature for 10 hours to complete the reaction. After completion of the reaction, the mixture was concentrated to about half the volume by evaporating dichloromethane under reduced pressure. The resultant colorless crystals were filtered. The crystals were then washed with a small amount of ether and dried to obtain 34.6 g of N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methylpyrimidin-2-yl) urea; m.p. 199°-202° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04586951
Source datasetuspto-grants-1986_05
ORD IDord-178020844ee249e4b3b0eaceec49e612
Source noteuspto-grants-1986_05