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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81837Generated: October 30, 2026

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

https://huagongshe.com/reaction/81837

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 numberUS08846705B2
Source datasetuspto-grants-2014_09
ORD IDord-4383bf394c16406590fdbae627d81dd2
Source noteuspto-grants-2014_09