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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757919Generated: November 3, 2026

4,6-dimethoxy-N-methyl-1,3,5-triazin-2-amine → N-[(4,6-dimethoxy-1,3,5-triazin-2-yl)(methyl)aminocarbonyl]-2-(methylsulfonyl)benzenesulfonamide

https://huagongshe.com/reaction/1757919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-dimethoxy-N-methyl-1,3,5-triazin-2-amineHCID 35017—
Reactant2-(Methanesulfonyl)benzene-1-sulfonyl isocyanateHCID 13093968—
SolventDichloromethaneHCID 6344—
ProductN-[(4,6-dimethoxy-1,3,5-triazin-2-yl)(methyl)aminocarbonyl]-2-(methylsulfonyl)benzenesulfonamideHCID 1309397088.8%

Reaction Steps

A solution of 2-methylsulfonylbenzenesulfonylisocyanate (2.1 g, 8.0 mmol) in dry methylene chloride (12 ml) was added to 2-methylamino-4,6-dimethoxy-1,3,5-triazine (1.0 g, 6.0 mmol) and a catalytic amount of 1,4-diaza[2.2.2]bicyclooctane. The mixture was stirred at room temperature overnight. The solvent was removed in-vacuo and 1-chlorobutane was added to the residue. The precipitated solid was filtered and dried to give N-[(4,6-dimethoxy-1,3,5-triazin-2-yl)(methyl)aminocarbonyl]-2-(methylsulfonyl)benzenesulfonamide (2.3 g) as a white powder, m.p. 160°-162.5°. The product showed characteristic singlets in the NMR at δ3.25 (NCH3), 3.40 (SO2CH3) and 4.0 (OCH3), and showed infrared absorption peaks at 1690, 1550, 1420, 1340, 1310 and 1150 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371391
Source datasetuspto-grants-1983_02
ORD IDord-65974dda1a244c0cbdfc9658747e52ab
Source noteuspto-grants-1983_02