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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645228Generated: October 31, 2026

Tetrahydrofuran → HCID 66775067, compound

https://huagongshe.com/reaction/1645228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 25007188HCID 25007188—
ReactantHCID 178418255HCID 178418255—
SolventWaterHCID 962—
ProductHCID 66775067HCID 66775067—

Reaction Conditions

Temperature0 °C

Reaction Steps

0.2 mL of a phenyl magnesium bromide 3.0 M tetrahydrofuran solution was added at 0° C. to a tetrahydrofuran (dehydrated) 3 mL solution of 200 mg of 5-(methylsulfonyl)-7-(5-(trifluoromethyl)pyridin-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidine, followed by stirring at 0° C. for 5 minutes. After completion of the reaction, water was added to the reaction liquid, followed by extraction with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=4/1) to obtain 93 mg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124760B2
Source datasetuspto-grants-2012_02
ORD IDord-778ccd8a6189424b8ea7417eb5655df9
Source noteuspto-grants-2012_02