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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434597Generated: October 26, 2026

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

https://huagongshe.com/reaction/434597

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
Reactant4-Bromothiophene-3-sulfonyl isocyanateHCID 20215704—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-aminocarbonyl]-3-thiophenesulfonamideHCID 13203334—

Reaction Conditions

Temperature10 °C

Reaction Steps

To 1.1 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine in 20 ml of tetrahydrofuran was added 2 g of 4-bromo-3-thiophenesulfonyl isocyanate in 5 ml of tetrahydrofuran. The mixture was then stirred and warmed on a steam bath for 15 minutes and allowed to stir at ambient temperature for 70 hours. It was then heated to reflux for 2 hours, cooled to 10° C., filtered and the filtrate evaporated. The residual oil was triturated to yield the desired product as a solid which after recrystallization from acetonitrile melted at 180°-183°, yield 1.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04398939
Source datasetuspto-grants-1983_08
ORD IDord-4c68d61476d74f48ba19370580407e08
Source noteuspto-grants-1983_08