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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266166Generated: October 30, 2026

Triethylamine → 2-Isopropyl-5-(4-methanesulfonyl-piperazin-1-yl)-4-methoxy-phenol

https://huagongshe.com/reaction/2266166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Isopropyl-4-methoxy-5-piperazin-1-yl-phenolHCID 59598675—
SolventDichloromethaneHCID 6344—
Product2-Isopropyl-5-(4-methanesulfonyl-piperazin-1-yl)-4-methoxy-phenolHCID 5959867316.2%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858632B2
Source datasetuspto-grants-2010_12
ORD IDord-f65595442ea24b46966dbf4284f8139e
Source noteuspto-grants-2010_12