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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41302Generated: October 25, 2026

4-Chlorobenzenesulfonyl chloride → (3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazine

https://huagongshe.com/reaction/41302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl (2R)-2-methylpiperazine-1-carboxylateHCID 10262201—
SolventDichloromethaneHCID 6344—
Product(3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazineHCID 1163046578.7%

Reaction Steps

To a solution of 1,1-dimethylethyl (2R)-2-methyl-1-piperazinecarboxylate (1.5 g, 07.5 mmol) in dry DCM (40 mL) was added triethylamine (2.59 mL, 18.8 mmol) and 4-chlorobenzenesulfonyl chloride (3.15 g, 10.5 mmol) and the reaction stirred at room temperature for 48 h. To the reaction was added resin supported-triamine (5 g) and the mixture stirred for 4 h. The reaction mixture was filtered and the filtrate washed with 0.5 M HCl (aq., 100 mL) followed by water (100 mL) before it was dried (MgSO4), filtered and the solvent removed in vacuo. The crude product was dissolved in DCM (40 mL) and TFA (10 mL) was added. The solution was stirred for 20 min. The solvent was evaporated and the residue tajen up in DCM (40 mL) and washed with 50% aqueous sodium bicarbonate (100 mL) followed by water (100 mL). The organic phase was dried (MgSO4), filtered and the solvent removed in vacuo to give the title compound (1.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530478B2
Source datasetuspto-grants-2013_09
ORD IDord-d72421402bcd411a95caa05e81703400
Source noteuspto-grants-2013_09