HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890827Generated: October 29, 2026
Diisopropylethylamine → 1-Formyl-4-[2-(benzimidazol-2-ylthio)ethyl]piperazine
https://huagongshe.com/reaction/890827
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(2-Hydroxyethyl)piperazine-1-carbaldehyde | HCID 9942213 | — |
| Reactant | (Cyanomethyl)trimethylphosphanium iodide | HCID 10514344 | — |
| Reactant | HCID 178527775 | HCID 178527775 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Propionitrile | HCID 7854 | — |
| Product | 1-Formyl-4-[2-(benzimidazol-2-ylthio)ethyl]piperazine | HCID 9961788 | 86.1% |
Reaction Steps
To a solution containing 1-formyl-4-(2-hydroxyethyl)piperazine (1.90 g, 12 mmol), 2-mercaptobenzimidazole (1.50 g, 10 mmol), and N,N-diisopropylethylamine (1.80 g, 14 mmol) in propionitrile (16 mL), cyanomethyltrimethylphosphonium iodide (2.80 g, 11.5 mmol) was added under argon, and the mixture was refluxed for 2 hours. After cooling, the reaction mixture was poured into water (100 mL), and the liquid was subjected to extraction with chloroform (100 mL×3) . The organic layer was washed with saturated brine, followed by drying over sodium sulfate anhydrate and removing the solvent through filtration. The thus-formed crude product was crystallized from acetone-diethyl ether, thereby yielding 2.50 g of 1-formyl-4-[2-(benzimidazol-2-ylthio)ethyl]piperazine (yield: 86%) as a colorless crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06998486B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-f8a06442bfd246029a215d279bc017e9 |
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| Source note | uspto-grants-2006_02 |
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