Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650345Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → N-(2-cyclopentyloxypyridin-3-ylsulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea

https://huagongshe.com/reaction/1650345

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Cyclopentyloxypyridin-3-ylsulfonamideHCID 19853721—
Reactant4-Methoxy-6-methyl-1,3,5-triazin-2-ylphenylcarbamateHCID 19995269—
Solvent1,4-DioxaneHCID 31275—
ProductN-(2-cyclopentyloxypyridin-3-ylsulfonyl)-N'-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)ureaHCID 1985372495.5%

Reaction Steps

To a mixture of 4.84 g of 2-cyclopentyloxypyridin-3-ylsulfonamide and 3.13 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene in 50 ml of absolute dioxan are added 5.46 g of N-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)phenylcarbamate at 20° to 25° C. The mixture is stirred for 1/2 hour, the precipitate is isolated and the filtrate is concentrated by evaporation. The residue is triturated with 10 ml of 2N hydrochloric acid and the crystals so obtained are isolated, washed with ether and water and dried, affording 7.79 g of N-(2-cyclopentyloxypyridin-3-ylsulfonyl)-N'-(4-methoxy-6methyl-1,3,5-triazin-2-yl)urea with a melting point of 170°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923995
Source datasetuspto-grants-1990_05
ORD IDord-c8be2d877bee45729f05aa981b3033de
Source noteuspto-grants-1990_05