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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831145Generated: October 31, 2026

7-Hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-1-benzopyran-2-one → 3,4-Dihydro-2H-quinoline-1-carboxylic Acid 3-(4-methoxy-phenyl)-4-methyl-2-oxo-2H-chromen-7-yl Ester

https://huagongshe.com/reaction/1831145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Hydroxy-3-(4-methoxyphenyl)-4-methyl-2H-1-benzopyran-2-oneHCID 5357627—
Reactant1-(3,4-Dihydroquinolin-1(2H)-ylcarbonyl)-3-methyl-1H-imidazol-3-ium IodideHCID 10959576—
Product3,4-Dihydro-2H-quinoline-1-carboxylic Acid 3-(4-methoxy-phenyl)-4-methyl-2-oxo-2H-chromen-7-yl EsterHCID 8658919859%

Reaction Steps

The title compound (130 mg, 59% yield, white solid) was prepared from 7-hydroxy-3-(4-methoxy-phenyl)-4-methyl-chromen-2-one (141 mg, 0.50 mmol) and 3-(3,4-dihydro-2H-quinoline-1-carbonyl)-1-methyl-3H-imidazol-1-ium iodide (188 mg, 0.51 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067517B2
Source datasetuspto-grants-2006_06
ORD IDord-e7f1d6c6f619410797f27613a2c33a20
Source noteuspto-grants-2006_06