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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910620Generated: October 30, 2026

Dimethylformamide → HCID 57584187, compound

https://huagongshe.com/reaction/910620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 57583919HCID 57583919—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 57584187HCID 57584187—

Reaction Steps

4-{1-[2-(Dimethylamino)ethyl]-2-oxo-1,2-dihydropyridin-3-yl}benzoic acid (1.46 g) was suspended in dichloroethane (15 ml), dimethylformamide (125 μL) was added, and oxalyl chloride (367 μL) was dropwise added dropwisely at room temperature. After stirring at room temperature for 30 minutes, the reaction mixture was evaporated under reduced pressure. A dichloromethane (10 ml)-pyridine (10 ml) solution of 2-amino-3-nitrophenol (499 mg) was added to the resulting residue, followed by stirring overnight at room temperature. The reaction suspension was filtered, and the filtrate was evaporated under reduced pressure. The substance collected by filtration and the filtration residue were dissolved in a mixed solvent of ethanol (14.6 mL)-water (14.6 mL), and an aqueous 1 M hydrochloric acid solution (3.24 mL) and iron (904 mg) were added, followed by heating under reflux for 3 hours. An aqueous saturated sodium hydrogencarbonate solution and chloroform were added to the reaction suspension, followed by vigorous stirring and filtration through Celite. The filtrate was extracted with chloroform, the organic layer was evaporated under reduced pressure, and the residue was purified by NH-silica gel column chromatography (chloroform:methanol=100:0 to 95:5) to obtain N-(2-amino-6-hydroxyphenyl)-4-{1-[2-(dimethylamino)ethyl]-2-oxo-1,2-dihydropyridin-3-yl}benzamide (600 mg) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022208B2
Source datasetuspto-grants-2011_09
ORD IDord-7a5792a6030a46a3b66a596b42cbfc89
Source noteuspto-grants-2011_09