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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227030Generated: October 30, 2026

1-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amide → HCID 57754568, compound

https://huagongshe.com/reaction/227030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 57754532—
SolventBromide ionHCID 259—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57754568HCID 57754568—

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 1.3 mL 0.5M 3-N,N-dimethylanilinemagnesium bromide. Yield: 97 mg of a yellow solid. LC-MSD, m/z for C24H20BrN3O2 [M+H]+=462.0, 464.0; HPLC retention time: 2.2 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-c71d38da5a5b4e5aa4be37aec1b59d2c
Source noteuspto-grants-2009_07