HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090351Generated: November 2, 2026
Triethylamine → 1-(Methanesulfonyl)-4-methylpiperazine
https://huagongshe.com/reaction/1090351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(Methanesulfonyl)-4-methylpiperazine | HCID 817770 | — |
Reaction Steps
A mixture of N-methylpiperazine (3.0 g, 29.9 mmol), triethylamine (3.6 g, 35.9 mmol) and methanesulfonyl chloride (Compound 19, 4.11 g, 35.9 mmol) in tetrahydrofuran (20 ml) was stirred at 0° C. for 2 hours. The mixture was filtered and the filtrate was evaporated to dryness to give a solid. The solid was redissolved in ethyl acetate and washed with water. Evaporation of the dried (magnesium sulfate) organic phase gave the title sulfonamide. 1HNMR(CDCl3): 2.35 (s, 3H), 2.53 (t, 4H, J=5.0 Hz), 2.79 (s, 3H) and 3.27 (t, 4H, J=5.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05081261 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-64a6c1fc458b4e65b8b1b9e06ea89865 |
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| Source note | uspto-grants-1992_01 |
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