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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362655Generated: October 31, 2026

Pyridine → HCID 54402406, compound

https://huagongshe.com/reaction/362655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 54565766HCID 54565766—
SolventWaterHCID 962—
ProductHCID 54402406HCID 54402406—

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 0.79 g (2.91 mmol) 1-(5-difluoromethoxy-1-methyl-3-pyrazolyl)-5-methyl-4-pyrazolecarboxamide, 0.46 g (5.85 mmol) pyridine and 20 ml 1,4-dioxane was cooled to 5° C. and 0.74 g (3.51 mmol) trifluoroacetic anhydride was added dropwise. The mixture was stirred for 3 hours at room temperature. It was then added to 100 ml water and extracted 4 times with ethyl acetate. The organic phase was dried over magnesium sulfate and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869686
Source datasetuspto-grants-1999_02
ORD IDord-7293964582cc49c3bbfd5e4cd21ef8ea
Source noteuspto-grants-1999_02