HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071651Generated: November 4, 2026
Triethylamine → (4-Cyano-5-methyl-4-(5-cyano-2-thienyl)hexyl]-4-[3-(5-cyano-2-thieny)propyl]piperazine
https://huagongshe.com/reaction/1071651
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-[3-(5-Cyano-2-thieny)propyl]piperazine | HCID 22393687 | — |
| Reactant | 4-Cyano-4-(5-cyano-2-thienyl)-5-methylhexyl iodide | HCID 22393730 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (4-Cyano-5-methyl-4-(5-cyano-2-thienyl)hexyl]-4-[3-(5-cyano-2-thieny)propyl]piperazine | HCID 10276667 | 92.9% |
Reaction Steps
In acetonitrile (3 ml) was dissolved 200 mg (0.56 mmol) of 4-cyano-5-methyl-4-(5-cyano-2-thienyl)hexyl iodide. To the mixture were added 78.0 μl (0.56 mmol) of triethylamine and 178 mg (0.76 mmol) of 1-[3-(5-cyano-2-thieny)propyl]piperazine, followed by stirring at 55° C. After 5 hours, the reaction solution was concentrated, and the residue was subjected to Cromatorex NH silica gel (ethyl acetate/hexane=1/2), to give 243 mg (0.52 mmol, 92.8%) of the title compound as a yellow syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06906072B1 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-b8df701236b54878a1e594ae684f4b53 |
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| Source note | uspto-grants-2005_06 |
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