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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003708Generated: October 31, 2026

Trifluoromethanesulfonic anhydride → HCID 18797032, compound

https://huagongshe.com/reaction/1003708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 18797012HCID 18797012—
CatalystCopper SulfateHCID 24462—
SolventPyridineHCID 1049—
ProductHCID 18797032HCID 1879703249.1%

Reaction Steps

Trifluoromethanesulfonic anhydride (0.21 ml, 1.25 mmol) was added dropwise with stirring to an ice cooled solution of 2-(4-(4-(3-cyanophenyl)benzoylamino)butyl)-7-hydroxy-1,2,3,4-tetrahydroisoquinoline (0.41 g, 0.96 mmol) in anhydrous pyridine (5 ml). After stirring at room temperature for 18 h. the mixture was poured into 10% aqueous copper (II) sulphate (100 ml). The mixture was extracted with ethyl acetate (2×50 ml) and the combined extracts washed with 10% aqueous copper (II) sulfate (2×50 ml). water (50 ml), dried (Na2SO4) and evaporated in vacuo. The residue was chromatographed on silica gel using 10-100% ethyl acetate-hexane gradient elution to afford the title compound (0.263 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046210
Source datasetuspto-grants-2000_04
ORD IDord-c5147f969b30476dabf129823cabc083
Source noteuspto-grants-2000_04