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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163584Generated: November 3, 2026

Dimethylformamide → Ethyl 7-Chloropyrimido[4,5-b]quinolin-4(3H)-one-2-carboxylate

https://huagongshe.com/reaction/2163584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiethyl OxalateHCID 7268—
ReactantSodium hydrideHCID 24758—
ReactantHCID 12594648HCID 12594648—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductEthyl 7-Chloropyrimido[4,5-b]quinolin-4(3H)-one-2-carboxylateHCID 135705337—

Reaction Steps

A mixture of 6-chloro-2-aminoquinoline-3-carboxamide (2.2 g., 0.01 mole), sodium hydride (0.52 g., 0.012 mole as 56% dispersion in oil) and N,N-dimethylformamide (20 ml.) is added to a solution of diethyl oxalate (5 ml.) and N,N-dimethylformamide (5 ml.). The reaction mixture is stirred for fifteen minutes, a second portion of sodium hydride (0.52 g., 0.012 mole) added and stirring continued for an additional fifteen minutes. Acetic acid (25.0 ml.) is cautiously added to the mixture followed by water (50 ml.). The tan precipitate is removed by filtration and dried (2.0 g. of crude ester). It is purified by chromatography on silica gel using chloroform:2B ethanol (99:1) as eluant. The product, recovered by concentration of the eluate, is recrystallized from acetic acid. Yield = 1.3 g. (37.3%). M.P. 260.5° C. (dec.). Mass spectra gave m/e = 303.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134981
Source datasetuspto-grants-1979_01
ORD IDord-20ae5aba1cec4a36abae2ef217740b46
Source noteuspto-grants-1979_01