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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403403Generated: October 31, 2026

Pyridine → HCID 86670562, compound

https://huagongshe.com/reaction/1403403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 70665235HCID 70665235—
SolventDichloromethaneHCID 6344—
ProductHCID 86670562HCID 86670562—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 2-oxo-3-(piperidin-1-yl)-1,2-dihydroquinoxaline-6-carboxylate (200 mg, 0.70 mmol) in dichloromethane (30 mL) was added pyridine (220 mg, 2.8 mmol) and then Tf2O (393 mg, 1.4 mmol) was added dropwise with stirring at 0° C. The resulting solution was stirred overnight at room temperature and then quenched by the addition of water (50 mL), extracted with dichloromethane (3×10 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to afford methyl 3-(piperidin-1-yl)-2-(trifluoromethylsulfonyloxy)quinoxaline-6-carboxylate as red solid (280 mg, crude).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-f403cf0c51f34f26be89f51001231578
Source noteuspto-grants-2014_12