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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704612Generated: October 25, 2026

2-Amino-4,6-dimethoxy-1,3,5-triazine → N-[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]-2-chlorobenzenesulfonamide

https://huagongshe.com/reaction/1704612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,6-dimethoxy-1,3,5-triazineHCID 27840—
ReactantBenzenesulfonyl isocyanate, 2-chloro-HCID 174071—
SolventDichloromethaneHCID 6344—
ProductN-[(4,6-dimethoxy-1,3,5-triazin-2-yl)aminocarbonyl]-2-chlorobenzenesulfonamideHCID 14835175—

Reaction Steps

To 15.6 g of 2-amino-4,6-dimethoxy-1,3,5-triazine in 300 ml of dry methylene chloride containing 0.1 g 1,4-diazabicyclo[2,2,2]octane was added 21 g 2-chlorobenzenesulfonyl isocyanate with stirring. The mixture was stirred for 16 hours and the resultant solid was removed by filtration. After washing the solid with 1-chlorobutane, the resulting product, N-[(4,6-dimethoxy-1,3,5-triazin-2-yl)-aminocarbonyl]-2-chlorobenzenesulfonamide melted at 188°-189° C. Infrared absorption analysis showed absorption peaks at 1740 cm-1, 1630 cm-1 and 1595 cm-1 which are typical for this type of compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04127405
Source datasetuspto-grants-1978_11
ORD IDord-3f5511fb26d5403e9c89d6032cc99f9b
Source noteuspto-grants-1978_11