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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615884Generated: November 2, 2026

Formamide → HCID 23030616, compound

https://huagongshe.com/reaction/1615884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantHydrogen PeroxideHCID 784—
ReactantSulfate IonHCID 1117—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl quinoline-6-carboxylateHCID 736812—
SolventWaterHCID 962—
SolventChloroform methanolHCID 21584188—
ProductHCID 23030616HCID 23030616—

Reaction Conditions

Temperature80 °C

Reaction Steps

4.0 g of 6-quinolinecarboxylic acid were suspended in 30 ml of MeOH, 2.0 ml of conc. sulfate was added under ice cooling, and the mixture was stirred at 70° C. for 22 hours. The reaction solution was concentrated under reduced pressure, and the residue was mixed with water and neutralized with potassium carbonate. The thus-precipitated solid was filtered and dried to obtain 4.28 g of 6-quinolinecarboxylic acid methyl ester. 0.5 g of the obtained ester body was dissolved in 5 ml of formamide, 0.15 ml of conc. sulfate, 0.05 g of ferrous sulfate hepta-hydrate, and 0.4 ml of 31% hydrogen peroxide were sequentially added thereto, and the mixture was stirred at 80° C. for 50 minutes. The reaction solution was mixed with water and alkalinized with potassium carbonate. 10% MeOH-chloroform was added, and insoluble matter was filtered using celite. The obtained filtrate was separated, the obtained organic layer was dried over anhydrous sodium sulfate and concentrated, and the obtained residue was washed with EtOH to obtain 0.15 g of 6-methoxycarbonyl-2-quinolinecarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765764B2
Source datasetuspto-grants-2014_07
ORD IDord-1ef323314fed4ce6bb434a8e6dfa25b8
Source noteuspto-grants-2014_07