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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285083Generated: October 29, 2026

2-Aminomethyl-4,6-dimethoxy-1,3,5-triazine → N'-[(4,6-dimethoxy-1,3,5-triazin-2-yl)methylaminocarbonyl]-N,N-dimethyl-1,2-benzenedisulfonamide

https://huagongshe.com/reaction/1285083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminomethyl-4,6-dimethoxy-1,3,5-triazineHCID 13392678—
Reactant2-(Dimethylsulfamoyl)benzene-1-sulfonyl isocyanateHCID 13392679—
SolventAcetonitrileHCID 6342—
ProductN'-[(4,6-dimethoxy-1,3,5-triazin-2-yl)methylaminocarbonyl]-N,N-dimethyl-1,2-benzenedisulfonamideHCID 1339268061.2%

Reaction Steps

A solution of 1.3 g of 2-(N,N-dimethylsulfamoyl)-benzenesulfonyl isocyanate in 25 ml of dry acetonitrile was treated at room temperature with 0.58 g of the product from Example 4. The resulting suspension was heated to 50°-55° C. for 11/2 hours and was then stirred at room temperature for an additional 15 hours. The solution was filtered and the collected solid washed well with 1-chlorobutane and then dried to yield 0.96 g of N'-[(4,6-dimethoxy-1,3,5-triazin-2-yl)methylaminocarbonyl]-N,N-dimethyl-1,2-benzenedisulfonamide as a light yellow powder, m.p. 183°-189° C., contaminated with some of the unreacted heterocyclic amine. Stirring the crude product with 5% hydrochloric acid at room temperature for 15 minutes followed by filtration gave the pure product as a white powder, m.p. 199°-201° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04565567
Source datasetuspto-grants-1986_01
ORD IDord-45e437ca06f8496f93117985f5cd0d68
Source noteuspto-grants-1986_01