HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38422Generated: October 28, 2026
Triethylamine → 2-Isopropyl-5-(4-methanesulfonyl-piperazin-1-yl)-4-methoxy-phenol
https://huagongshe.com/reaction/38422
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Isopropyl-4-methoxy-5-piperazin-1-yl-phenol | HCID 59598675 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Isopropyl-5-(4-methanesulfonyl-piperazin-1-yl)-4-methoxy-phenol | HCID 59598673 | 16.2% |
Reaction Steps
To a stirring solution of 2-Isopropyl-4-methoxy-5-piperazin-1-yl-phenol (0.47 g, 1.88 mmol) in dichloromethane at 0° C. under nitrogen was added triethylamine (0.26 mL, 1.89 mmol), followed by methanesulfonyl chloride (0.15 mL, 1.89 mmol). The reaction mixture was stirred at 0° C. for five minutes, and then allowed to warm to room temperature. The reaction mixture was partitioned between dichloromethane and water, and the organic layer was separated, washed with water, dried (MgSO4), filtered, and evaporated under reduced pressure. The residue was purified via flash chromatography (hexanes:EtOAc 3:2) to afford 0.1 g (16%) of 2-Isopropyl-5-(4-methanesulfonyl-piperazin-1-yl)-4-methoxy-phenol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524725B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-ce245b4715e048958e79271a40412aad |
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| Source note | uspto-grants-2013_09 |
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