HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516593Generated: October 26, 2026
Potassium Phosphate, Tribasic → 2-(3-Cyano-4-phenylpyrrole-1-yl)isonicotinic acid ethyl ester
https://huagongshe.com/reaction/1516593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | trans-N,N'-dimethyl-1,2-cyclohexanediamine | HCID 2733821 | — |
| Reactant | 4-Phenyl-1H-pyrrole-3-carbonitrile | HCID 3721460 | — |
| Reactant | Ethyl 2-bromoisonicotinate | HCID 3847769 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(3-Cyano-4-phenylpyrrole-1-yl)isonicotinic acid ethyl ester | HCID 59477832 | 35% |
Reaction Steps
To a solution of 4-phenyl-1H-pyrrole-3-carbonitrile (0.1 g) in toluene (0.70 mL) were added 2-bromo-isonicotinic acid ethyl ester (0.19 g), potassium phosphate (0.31 g), (1R,2R)-(−)—N,N′-dimethylcyclohexane-1,2-diamine (0.02 g) and copper iodide (0.007 g) at room temperature, and this mixture was stirred at 110° C. for 24 hours. The insoluble material was removed by filtration through Celite, and this filtrate was concentrated. This obtained residue was purified by column chromatography on silica gel (eluent: ethyl acetate/n-hexane=10/90−66/34) to give the title compound (0.066 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08227500B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-1f592b469abe45179af6c2d684686c14 |
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| Source note | uspto-grants-2012_07 |
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