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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227084Generated: October 26, 2026

1-(3-Chloro-benzyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amide → 1-(3-Chloro-benzyl)-3-(4-methoxy-benzoyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/227084

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chloro-benzyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 57754615—
ReactantHCID 178491912HCID 178491912—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Chloro-benzyl)-3-(4-methoxy-benzoyl)-1H-quinolin-4-oneHCID 57754784—

Reaction Steps

Experimental conditions analogous to those described for Step 6 of Example 60, from 300 mg (0.84 mmol) of 1-(3-chloro-benzyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amide in 3 mL THF and 3.7 mL 0.5M 4-methoxyphenylmagnesium bromide. Yield: 168 mg of a white solid. LC-MSD, m/z for C24H18ClNO3 [M+H]+=404.1, 406.0; HPLC retention time: 2.4 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-91a7c42bb7824b99a5c4610f754a7375
Source noteuspto-grants-2009_07