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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713044Generated: October 25, 2026

Potassium Carbonate → 4-[2-(4-Nitro-phenyl)-6-oxo-4-thioxo-6H-1-oxa-3b,5-diaza-cyclopenta[a]pentalen-5-yl]-butyronitrile

https://huagongshe.com/reaction/1713044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Isothiocyanato-butyronitrileHCID 15134644—
Reactant2-(4-nitro-phenyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid ethyl esterHCID 59463445—
ReactantHCID 86618327HCID 86618327—
SolventEthanolHCID 702—
Product4-[2-(4-Nitro-phenyl)-6-oxo-4-thioxo-6H-1-oxa-3b,5-diaza-cyclopenta[a]pentalen-5-yl]-butyronitrileHCID 11653778—

Reaction Conditions

Temperature110 °C

Reaction Steps

2-(4-nitro-phenyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid ethyl ester (60.97 mg, 0.21 mmol), prepared as described hereinabove (see, preparation of Compound 1), 4-isothiocyanato-butyronitrile (664 mg, 2.1 mmol) and a fine powder of anhydrous K2CO3 (27.6 mg, 0.2 mmol) are mixed together in a sealed tube, provided with a magnetic stirrer, and the mixture is heated at 110° C. for 2 hours. The mixture is cooled to room temperature, ethanol is added (2 ml), and the formed precipitate is filtered. The crude product is recrystallized from ethanol to give Compound 35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795255B2
Source datasetuspto-grants-2010_09
ORD IDord-f7bf6337c3444f61a0f6334556d517b1
Source noteuspto-grants-2010_09