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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853979Generated: October 30, 2026

Pyridine → HCID 86703405, compound

https://huagongshe.com/reaction/1853979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178469345HCID 178469345—
SolventDichloromethaneHCID 6344—
ProductHCID 86703405HCID 8670340577.8%

Reaction Steps

Trifluoromethanesulfonic anhydride (5.23 g, 18.5 mmol) was added to a cooled solution of ethyl 6-hydroxy-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylate (4.2 g, 16.9 mmol) and pyridine (1.46 g, 18.5 mmol) in DCM (60 mL); and it was allowed to stirred at room temperature for 2 h. After completion of the reaction, saturated NaHCO3 solution (60 mL) was added to it and extraction was carried out using DCM (30 mL×3). The combined organic layers were washed with water (100 mL); brine (100 mL); dried over anhydrous Na2SO4; filtered and concentrated under reduced pressure. The residue was finally purified by silica gel column chromatography to provide pure the desired intermediate (5 g, 77.8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962620B2
Source datasetuspto-grants-2015_02
ORD IDord-c75174d59e5c4d09b467b6748c0d04d6
Source noteuspto-grants-2015_02