HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354260Generated: November 3, 2026
Diisopropylethylamine → 1-[2-(5-Fluorobenzimidazol-2-ylthio)ethyl]-4-formylpiperazine
https://huagongshe.com/reaction/1354260
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-fluoro-1H-benzimidazole-2-thiol | HCID 3434885 | — |
| Reactant | 4-(2-Hydroxyethyl)piperazine-1-carbaldehyde | HCID 9942213 | — |
| Reactant | (Cyanomethyl)trimethylphosphanium iodide | HCID 10514344 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Propionitrile | HCID 7854 | — |
| Product | 1-[2-(5-Fluorobenzimidazol-2-ylthio)ethyl]-4-formylpiperazine | HCID 23116158 | 80% |
Reaction Steps
1-Formyl-4-(2-hydroxyethyl)piperazine (1.20 g, 7.6 mmol), 5-fluoro-2-mercaptobenzimidazole (1.28 g, 7.6 mmol), and diisopropylethylamine (3.93 g, 30.4 mmol) was dissolved in propionitrile (50 mL), and cyanomethyltrimethylphosphonium iodide (7.39 g, 30.4 mmol) was added to the mixture, followed by stirring for one hour at 92° C. under argon. The reaction mixture was allowed to cool and then poured into water (100 mL), followed by extraction with chloroform (100 mL×3) The resultant organic layer was washed with saturated brine and then dried over sodium sulfate anhydrate, followed by concentration under reduced pressure. The crude product was crystallized from acetone-ether, to thereby yield 1-[2-(5-fluorobenzimidazol-2-ylthio)ethyl]-4-formylpiperazine (1.87 g, yield 80%) as a brown crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07223764B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-27a4d1b7b6ce4a5a8e5779686c918492 |
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| Source note | uspto-grants-2007_05 |
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