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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905607Generated: October 28, 2026

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamide

https://huagongshe.com/reaction/1905607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
Reactant2-(beta-Chloroethoxycarbonyl)benzenesulfonylisocyanateHCID 13920549—
SolventDichloromethaneHCID 6344—
ProductN-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamideHCID 1317669680.1%

Reaction Steps

To 0.7 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine in 10 ml anhydrous methylene chloride solvent was added 1.45 g 2-(β-chloroethoxycarbonyl)benzenesulfonyl isocyanate with stirring at ambient temperature. The mixture was thereafter stirred for sixteen hours. The solvent was evaporated under reduced pressure and the residue triturated with hexane and filtered to yield 1.72 g of compound which melted at 167°-170° C. The solid showed infrared absorption peaks at 1700 and 1705 cm-1, consistent for N-[(4-methoxy-6-methyl-1,3,5-triazin-2yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04647303
Source datasetuspto-grants-1987_03
ORD IDord-10957fcf2b414d24b0187a1b5c719e16
Source noteuspto-grants-1987_03