HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972692Generated: November 4, 2026
Triethylamine → 3-(1-Propyn-1-yl)-1-(2-thiophenylsulfonyl)piperazine
https://huagongshe.com/reaction/1972692
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Thiophenesulfonyl chloride | HCID 85518 | — |
| Reactant | 2-Propynylpiperazine | HCID 66583809 | — |
| Reactant | 2-(1-Propyn-1-yl)piperazine bis(trifluoroacetate) | HCID 86670441 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(1-Propyn-1-yl)-1-(2-thiophenylsulfonyl)piperazine | HCID 66584007 | — |
Reaction Steps
The 2-(1-propyn-1-yl)piperazine bis(trifluoroacetate (110 mg, 0.312 mmol) was dissolved in CH2Cl2 in a 50 mL round-bottomed flask and was then cooled to 0° C. To this solution was added an excess of triethylamine (152 μL, 1.093 mmol) followed by thiophene-2-sulfonyl chloride (57.0 mg, 0.312 mmol, Sigma-Aldrich, St. Louis, Mo.). The mixture was warmed slowly to room temperature and stirred for 2 h. Afterwards, the mixture was concentrated and absorbed onto silica gel. The crude material was purified via column chromatography (about 40 g silica gel, 0% to 10% MeOH in CH2Cl2) to give 3-(1-propyn-1-yl)-1-(2-thiophenylsulfonyl)piperazine (42 mg) as a foamy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431563B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-68114e47dbb64e71a46f68c3ddfdc81d |
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| Source note | uspto-grants-2013_04 |
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