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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980787Generated: October 30, 2026

2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide → N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide

https://huagongshe.com/reaction/1980787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamideHCID 13489814—
ReactantMethyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamateHCID 14404501—
ReactantTrimethylaluminumHCID 16682925—
SolventDichloromethaneHCID 6344—
ProductN-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamideHCID 1348986517.6%

Reaction Steps

By the procedure of Example 14, 2 g of 2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide, prepared in Example 19, was reacted in 100 ml of methylene chloride with 0.7 g of trimethylaluminum (5 ml of 2M toluene solution) followed by 1.7 g of methyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate. After work up and evaporation of the methylene chloride solvent, the residue was triturated with ethyl acetate to yield 0.6 g of the title compound; m.p. 221°-224° C. The IR spectrum showed a carbonyl absorption at 1700 cm-1 indicative for a sulfonylurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04511392
Source datasetuspto-grants-1985_04
ORD IDord-70198f55f61f447c819e7aa38bdd886a
Source noteuspto-grants-1985_04