Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70671Generated: October 29, 2026

Anisole → HCID 58452288, compound

https://huagongshe.com/reaction/70671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
Reactant3-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-oxo-1,2-dihydropyridin-3-yl)propanamideHCID 67398756—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 58452288HCID 5845228823.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Anisole (0.3 mL) was added to a solution of 3-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-oxo-1,2-dihydropyridin-3-yl)propanamide (82.6 mg) in trifluoroacetic acid (0.6 mL), and the mixture was stirred at 80° C. for 19 hours. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform:methanol=1:0→9:1) to give the title compound as a colorless oil (14 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822503B2
Source datasetuspto-grants-2014_09
ORD IDord-cb16e73121264b78bf32b6818ad95324
Source noteuspto-grants-2014_09