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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391844Generated: November 2, 2026

Hydrochloric Acid → Penoxsulam

https://huagongshe.com/reaction/1391844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,5-DimethylpyridineHCID 11565—
Reactant5,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amineHCID 11446888—
Reactant2-(2,2-Difluoroethoxy)-6-(trifluoromethyl)benzene-1-sulfonyl chlorideHCID 16050308—
CatalystDimethyl SulfoxideHCID 679—
SolventAcetonitrileHCID 6342—
ProductPenoxsulamHCID 1178497591%

Reaction Steps

2-Amino-5,8-dimethoxy[1,2,4]triazolo[1,5-c]pyrimidine (19.5 g, 0.10 mol) and 2-(2,2-difluoro-ethoxy)-6-(trifluoromethyl)benzenesulfonyl chloride (32.5 g, 0.10 mol) were combined in acetonitrile (45 mL) and 3,5-lutidine (17 g, 93% technical, ˜0.16 mol) at room temperature. After 10 minutes, DMSO (0.20 g, 0.0026 mol) was added and the reaction slurry was stirred at room temperature for 24 hours. The mixture was then warmed to 48° C. and acidified by the addition of 2 N HCl (100 mL) over 30 minutes, during which the temperature was allowed to fall to ˜38° C. The warm mixture was stirred for one hour, then cooled to 10° C. The precipitated solids were filtered, washed with water (30 mL), washed with methanol (75 mL), and dried under vacuum to afford 44 g of product as a light tan solid assaying at 98 wt % (89% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07339058B2
Source datasetuspto-grants-2008_03
ORD IDord-c3f0c60a311d4c598e23d9d4515a6d1b
Source noteuspto-grants-2008_03