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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066104Generated: October 26, 2026

Diisopropylethylamine → (3S)-3-methyl-1-({4-[(trifluoromethyl)oxy]phenyl}sulfonyl)piperazine

https://huagongshe.com/reaction/2066104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactantp-(Trifluoromethoxy)benzenesulphonyl chlorideHCID 523102—
Reactanttert-Butyl (2S)-2-methylpiperazine-1-carboxylateHCID 10081508—
SolventDichloromethaneHCID 6344—
Product(3S)-3-methyl-1-({4-[(trifluoromethyl)oxy]phenyl}sulfonyl)piperazineHCID 5915207563.2%

Reaction Steps

A solution of 4-[(trifluoromethyl)oxy]benzenesulfonyl chloride (3.25 g, 12.48 mmol), 1,1-dimethylethyl(2S)-2-methyl-1-piperazinecarboxylate (2.5 g, 12.48 mmol) and DIPEA (4.58 ml, 26.2 mmol) in DCM (200 ml) was stirred at room temperature overnight. The mixture was washed with saturated aqueous NaHCO3 then brine. The organics were concentrated under vacuum, then re-dissolved in dioxane (200 ml). A 4M solution of HCl in dioxane (20 ml) and water (0.5 ml) were added and the mixture stirred overnight. The mixture was concentrated under vacuum, applied to an SCX-2 cartridge (20 g) washing with MeOH and eluting with 0.5M NH3 in MeOH; concentration under vacuum gave the title compound as a white solid (2.56 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288388B2
Source datasetuspto-grants-2012_10
ORD IDord-60bb346affca4dd4a1cdb16f1fa0da31
Source noteuspto-grants-2012_10