Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052987Generated: November 1, 2026

Sodium hydride → HCID 67250969, compound

https://huagongshe.com/reaction/1052987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantIsocyanateHCID 105034—
ReactantEthyl 4-aminoquinoline-3-carboxylateHCID 4570951—
ReactantHCID 178418790HCID 178418790—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67250969HCID 67250969—

Reaction Steps

To a solution of a 4-amino-quinoline-3-carboxylic acid ethyl ester derivative (0.50 mmol) in 10 mL anhydrous DMF is added sodium hydride (4 eq., 2.0 mmol) and stirred at room temperature for 30 min. To this solution an isocyanate or isothiocyanate (1.5-4 eq. 2.0 mmol) is added. The resulting reaction mixture is stirred for 18 h at room temperature or at 100° C. After completion of the reaction, the mixture is poured into water (20 mL) and extracted with ethyl acetate (2×25 mL). The organic extracts are combined, washed with water (2×25 mL), brine (2×25 mL), dried over Na2SO4 and concentrated in vacuo to give the crude product. The residue is then purified by silica gel chromatography using dichloromethane-ethyl acetate to provide desired 1H-pyrimido[5,4-c]quinoline-2,4-dione or thio-ketone derivative.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393245B2
Source datasetuspto-grants-2016_07
ORD IDord-7b3cb3500c9c4b54be48b389c05e1e9f
Source noteuspto-grants-2016_07