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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227057Generated: 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-(6-ethyl-pyridine-3-carbonyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/227057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 57754532—
Reactant2-Ethyl-5-iodo-pyridineHCID 66879476—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product1-(6-Bromo-pyridin-2-ylmethyl)-3-(6-ethyl-pyridine-3-carbonyl)-1H-quinolin-4-oneHCID 57754505—

Reaction Steps

Experimental conditions analogous to those described for Step 6 of Example 60 from 120 mg (0.30 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 153 mg (0.66 mmol) of 2-ethyl-5-iodo-pyridine in 1 mL THF with 0.34 mL 2M isopropylmagnesium chloride. Yield: 62 mg of a white powder. LC-MSD, m/z for C23H18BrN3O2 [M+H]+=448.0, 450.0; HPLC retention time: 1.6 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-7d1d925aa51845d8bd90a3cf6a55f00a
Source noteuspto-grants-2009_07