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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Isothiocyanato-butyronitrile | HCID 15134644 | — |
| Reactant | 2-(4-nitro-phenyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid ethyl ester | HCID 59463445 | — |
| Reactant | HCID 86618327 | HCID 86618327 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[2-(4-Nitro-phenyl)-6-oxo-4-thioxo-6H-1-oxa-3b,5-diaza-cyclopenta[a]pentalen-5-yl]-butyronitrile | HCID 11653778 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795255B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-f7bf6337c3444f61a0f6334556d517b1 |
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| Source note | uspto-grants-2010_09 |
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