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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615533Generated: 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/615533

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 1310332285%

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 28.5 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 numberUS04500342
Source datasetuspto-grants-1985_02
ORD IDord-32218f8688e7402bb6fe566c05e97666
Source noteuspto-grants-1985_02