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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227058Generated: November 3, 2026

Tetrahydrofuran → 1-(6-Bromo-pyridin-2-ylmethyl)-3-(4-methoxy-2-methyl-benzoyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/227058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 57754532—
SolventHCID 178491917HCID 178491917—
Product1-(6-Bromo-pyridin-2-ylmethyl)-3-(4-methoxy-2-methyl-benzoyl)-1H-quinolin-4-oneHCID 57754529—

Reaction Steps

Experimental conditions analogous to those described for Step 6 of Example 60 from 90 mg (0.22 mmol) of 1-(6-bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amide in 1.5 mL THF and 0.98 mL 0.5M 4-methoxy-2-methylphenylmagnesium bromide. Yield: 41 mg of a white solid. LC-MSD, m/z for C24H19BrN2O3 [M+H]+=463.0, 465.0; HPLC retention time: 2.4 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-6b9541a4b0854e99946b0c73d8802423
Source noteuspto-grants-2009_07