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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475851Generated: November 3, 2026

Pyridine → Quinolin-7-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/1475851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant7-HydroxyquinolineHCID 135426866—
SolventDichloromethaneHCID 6344—
ProductQuinolin-7-yl trifluoromethanesulfonateHCID 5929611586.7%

Reaction Steps

Trifluoromethanesulfonic anhydride (1.40 mL, 8.32 mmol) was added dropwise via a syringe to a solution of quinolin-7-ol (930 mg, 6.41 mmol), and pyridine (1.05 mL, 13.0 mmol) in anhydrous dichloromethane (50 mL) at 0° C. After addition the ice bath was removed and the reaction was allowed to warm to room temperature and stirred overnight. The reaction was concentrated and purified via flash chromatography using an Analogix SF25-40g column and eluant of ethyl acetate in heptane (0-40%) to afford the title compound as an orange-white solid (1.54 g, 86.7%). LC-MS m/z 278.4 (M+1). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.42-7.57 (m, 2H) 7.95 (d, J=8.98 Hz, 1H) 8.05 (d, J=2.54 Hz, 1H) 8.20-8.29 (m, 1H) 8.97-9.06 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018384B2
Source datasetuspto-grants-2015_04
ORD IDord-f44f4b748e6b464aa0c843bf171fa495
Source noteuspto-grants-2015_04