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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283163Generated: November 3, 2026

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

https://huagongshe.com/reaction/1283163

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 numberUS03974161
Source datasetuspto-grants-1976_08
ORD IDord-7fde00ed3ecb435f85c66b32161edb09
Source noteuspto-grants-1976_08