HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972658Generated: November 4, 2026
Triethylamine → 3-((2-Methoxy-3-pyridinyl)methyl)-1-(2-thiophenylsulfonyl)piperazine
https://huagongshe.com/reaction/1972658
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Thiophenesulfonyl chloride | HCID 85518 | — |
| Reactant | 2-((2-Methoxy-3-pyridinyl)methyl)piperazine | HCID 66582930 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 3-((2-Methoxy-3-pyridinyl)methyl)-1-(2-thiophenylsulfonyl)piperazine | HCID 66583202 | 33.8% |
Reaction Steps
To a 100-mL round-bottomed flask was added 2-((2-methoxy-3-pyridinyl)methyl)piperazine (350 mg, 1.69 mmol), triethylamine (0.353 mL, 2.54 mmol), and 2-thiophenesulfonyl chloride (0.34 mL, 1.86 mmol, Aldrich, St. Louis, Mo.) in DCM (5 mL). The reaction mixture was stirred at 0° C. for 1 h. The reaction mixture was diluted with saturated NaHCO3 (5 mL) and extracted with EtOAc (2×30 mL). The organic extract was washed with saturated NaCl (5 mL) and dried over Na2SO4. The solution was filtered and concentrated in vacuo to give the crude material as a yellow glass. The crude product was purified by silica gel chromatography, eluting with 10% MeOH/EtOAc to give 3-((2-methoxy-3-pyridinyl)methyl)-1-(2-thiophenylsulfonyl)piperazine (202 mg) as a white 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-7648458c42374fd9a7491d058b85f988 |
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| Source note | uspto-grants-2013_04 |
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