Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279736Generated: October 27, 2026

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea

https://huagongshe.com/reaction/279736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
Reactant2-BiphenylylsulfonylisocyanateHCID 13103320—
CatalystDabcoHCID 9237—
SolventAcetonitrileHCID 6342—
SolventO-XyleneHCID 7237—
ProductN-2-biphenylylsulfonyl-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)ureaHCID 13103322880.2%

Reaction Steps

14.0 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine were suspended in 100 ml of dry acetonitrile, and then 0.1 g of 1,4-diazabicyclo[2,2,2]octane was added thereto. To this mixture was added dropwise a solution of 2.5 g of 2-biphenylylsulfonyl isocyanate in 30 ml of xylene over an hour. During this addition, the reaction was accompanied by slight heat generation, and therefore cooling was applied as necessary. After the addition, the reaction was continued at room temperature for 5 hours and then at 40° C. for 5 hours. After allowing the mixture to cool to room temperature, the precipitated colorless crystals were filtered, washed with ether and dried to obtain 33.9 g of N-2-biphenylylsulfonyl-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl) urea; m.pt. 190°-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04586951
Source datasetuspto-grants-1986_05
ORD IDord-bf5ab0754ea245d285bd98105931f910
Source noteuspto-grants-1986_05