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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227082Generated: October 30, 2026

2-Chloro-5-iodopyridine → 1-(3-Chloro-benzyl)-3-(6-chloro-pyridine-3-carbonyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/227082

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-iodopyridineHCID 4397176—
Reactant1-(3-Chloro-benzyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 57754615—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Chloro-benzyl)-3-(6-chloro-pyridine-3-carbonyl)-1H-quinolin-4-oneHCID 57754604—

Reaction Steps

Experimental conditions analogous to those described for Step 6 of Example 60, from 600 mg (1.68 mmol) of 1-(3-chloro-benzyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amide in 4 mL THF and 887 mg (3.70 mmol) of 2-chloro-5-iodo-pyridine in 4 mL THF with 1.93 mL 2M isopropylmagnesium chloride. Yield: 418 mg of a white powder. LC-MSD, m/z for C22H14Cl2N2O2 [M+H]+=409.0, 411.0; HPLC retention time: 3.3 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-aed9548572ca472ca6b60dad86b221e3
Source noteuspto-grants-2009_07