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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112249Generated: October 31, 2026

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

https://huagongshe.com/reaction/1112249

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 stirred continued for an additional 15 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 numberUS04120962
Source datasetuspto-grants-1978_10
ORD IDord-949570828a714a9fb3b476a36bc67bfe
Source noteuspto-grants-1978_10