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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366899Generated: October 30, 2026

Dimethyl Sulfoxide → N-(5,8-Dimethoxy[1,2,4]triazolo-[1,5-c]pyrimidin 2-yl)-2-methoxy-4-(trifluoromethyl)-3-pyridinesulfonamide

https://huagongshe.com/reaction/366899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPyridineHCID 1049—
Reactant5,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amineHCID 11446888—
Reactant2-Methoxy-4-(trifluoromethyl)pyridine-3-sulfonyl chlorideHCID 18539798—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductN-(5,8-Dimethoxy[1,2,4]triazolo-[1,5-c]pyrimidin 2-yl)-2-methoxy-4-(trifluoromethyl)-3-pyridinesulfonamideHCID 18366179—

Reaction Steps

A mixture of 0.75 g (93.8 mmol) of 2-amino-5,8-dimethoxy[1,2,4]triazolo[1,5-c]pyrimidine, 2.1 g (7.6 mmol) of 2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonyl chloride, and 10 mL of dry acetonitrile was prepared and to this was added at ambient temperature with stirring and means to exclude moisture from the system 0.61 mL (7.6 mmol) of dry pyridine, 43 microliters (0.6 mmol) of dry dimethyl sulfoxide, and a small quantity of dry 4A molecular sieves. The mixture was stirred for 5 days. Another 1.0 g (3.4 mmol) of 2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonyl chloride and 0.30 mL (3.5 mmol) of dry pyridine were added and the mixture stirred another 2 days. Another 0.30 mL (3.5 mmol) of dry pyridine was added and stirring continued for 4 more days. The mixture was then diluted with 100 mL of dichloromethane and the resulting mixture was washed with 2×100 mL of 2N aqueous hydrochloric acid, dried over magnesium sulfate, and concentrated by evaporation under reduced pressure. The tan solid residue was chromatographed on silica gel eluting with a mixture of dichloromethane and ethanol to obtain 0.90 g (54 percent of theory) of the title compound as a white solid melting at 214-216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130335
Source datasetuspto-grants-2000_10
ORD IDord-e5e1f0b9cf6644af87ab602f1f54bb24
Source noteuspto-grants-2000_10