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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732802Generated: October 26, 2026

Nitrogen → Trifluoromethanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)benzoyl]-naphthalen-2-yl ester

https://huagongshe.com/reaction/732802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
Reactant6-Methoxy-1-[4-(2-piperidin-1-yl-ethoxy)-benzoyl]-naphthalen-2-olHCID 21931628—
SolventDichloromethaneHCID 6344—
ProductTrifluoromethanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)benzoyl]-naphthalen-2-yl esterHCID 11685250—

Reaction Steps

Dissolve (2-hydroxy-6-methoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone in CH2Cl2 (10 volumes) in a three neck round bottom flask equipped with a stir bar and N2 source and chill to 0° C. in an ice/brine bath. Add pyridine (1.3 eq.). Add trifluoromethanesulfonyl chloride (1.2 eq.) via syringe over 15 minutes. After about 15 minutes, quench the reaction with H2O (10 volumes), wash with 1 N aqueous HCl (5 volumes) and 1.0 N aqueous NaHCO3, and dry over Na2SO4. Obtain the title compound in quantitative yield after concentration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585977B2
Source datasetuspto-grants-2009_09
ORD IDord-10f401f051734b89b26c96af279a0449
Source noteuspto-grants-2009_09