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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556418Generated: October 30, 2026

Ethanol → HCID 11587404, compound

https://huagongshe.com/reaction/556418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantBenzoyl isocyanateHCID 78210—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 9971786HCID 9971786—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 11587404HCID 1158740485.2%

Reaction Steps

1.0 g (6.8 mmol) benzoylisocyanate is added to 1.0 g (3.4 mmol) 3-amino-4-methyl-6-phenyl-furo[2,3-b]pyridine-2-carboxylic acid ethyl ester (described in Wagner G., Prantz J. Pharmazie 1990, 45, 213-214) in 20 ml absolute acetone and stirred at room temperature for 30 minutes. The solvent is removed and the precipitate precipitated after the addition of water is sucked off and dried. The resulting precipitate is refluxed with 0.46 g (6.8 mmol) NaOEt and 20 ml ethanol for 15 min. Then, 20 ml water is added, the precipitate is sucked off, washed with some ethanol and dried. 0.85 g (85%) 9-methyl-7-phenyl-pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2,4-dione is obtained

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058285B2
Source datasetuspto-grants-2011_11
ORD IDord-418873c7e0ca4778a6200c8c284dfb89
Source noteuspto-grants-2011_11