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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

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 numberUS08524725B2
Source datasetuspto-grants-2013_09
ORD IDord-ce245b4715e048958e79271a40412aad
Source noteuspto-grants-2013_09