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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259861Generated: October 25, 2026

Dichloromethane → 2-(4-Nitrophenyl)-4-quinolinecarboxylic acid methyl ester

https://huagongshe.com/reaction/1259861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Nitrophenylboronic acidHCID 2773552—
ReactantMethyl 2-chloroquinoline-4-carboxylateHCID 5202936—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
Product2-(4-Nitrophenyl)-4-quinolinecarboxylic acid methyl esterHCID 342037078.8%

Reaction Conditions

Temperature85 °C

Reaction Steps

PdCl2(dppf).CH2Cl2 (184 mg, 0.23 mmol), tripotassium phosphate (624 mg, 4.51 mmol), and 4-nitrophenylboronic acid (958 mg, 4.51 mmol) were added to a 1,4-dioxane (5 mL)/DMF (1 mL) mixed solution of 2-chloro-4-quinolinecarboxylic acid methyl ester (500 mg, 2.26 mmol) obtained in Reference Example 3, and the mixture was heated with stirring overnight at 85° C. in an argon atmosphere. After the reaction solution was concentrated, to the residue, a saturated aqueous solution of sodium chloride and methylene chloride were added, and insoluble matter was filtered off through celite. After that, the residue was subjected to extraction with methylene chloride and dried over anhydrous sodium sulfate. The solvent was distilled off, and the obtained residue was purified by silica gel column chromatography to obtain 2-(4-nitrophenyl)-4-quinolinecarboxylic acid methyl ester (549 mg, 1.78 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466290B2
Source datasetuspto-grants-2013_06
ORD IDord-eee545d12a32431c9e711717562ac72d
Source noteuspto-grants-2013_06