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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434601Generated: October 25, 2026

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

https://huagongshe.com/reaction/434601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
Reactant4-Nitrothiophene-2-sulfonyl isocyanateHCID 20215702—
SolventAcetonitrileHCID 6342—
ProductN-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-4-nitrothiophene-2-sulfonamideHCID 13472988—

Reaction Steps

To 1.4 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine suspended in 25 ml of anhydrous acetonitrile with stirring at ambient temperature was added 2.4 g of 4-nitrothiophene-2-sulfonyl isocyanate. After stirring for sixteen hours at ambient temperature, the product which was present as a precipitate was removed by filtration and washed with 1-chlorobutane. It melted at 188° with decomposition and showed infrared absorption spectrum peaks at 1740, 1600 and 1560 cm-1 consistent for the desired aminocarbonylsulfonamide structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04398939
Source datasetuspto-grants-1983_08
ORD IDord-805a8920dbc04c2ebd3b16277aba02ef
Source noteuspto-grants-1983_08