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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227055Generated: October 30, 2026

1-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amide → 1-(6-Bromo-pyridin-2-ylmethyl)-3-(5-methyl-pyridine-2-carbonyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/227055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 57754532—
SolventTetrahydrofuranHCID 8028—
SolventHCID 178426145HCID 178426145—
Product1-(6-Bromo-pyridin-2-ylmethyl)-3-(5-methyl-pyridine-2-carbonyl)-1H-quinolin-4-oneHCID 57754728—

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 mL THF and 1.96 mL 0.25M 5-methyl-2-pyridylmagnesium bromide. Yield: 33 mg of a white solid. LC-MSD, m/z for C22H16BrN3O2 [M+H]+=434.0, 436.0; HPLC retention time: 2.0 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-5b86caf117da4d4aba83a792ee71151d
Source noteuspto-grants-2009_07