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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365443Generated: October 31, 2026

Diisopropylethylamine → 1,1-dimethylethyl(2S)-4-[(4-cyano-2-methylphenyl)sulfonyl]-2-methyl-1-piperazinecarboxylate

https://huagongshe.com/reaction/2365443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl (2S)-2-methylpiperazine-1-carboxylateHCID 10081508—
Reactant1251110-16-3HCID 54594768—
SolventDichloromethaneHCID 6344—
Product1,1-dimethylethyl(2S)-4-[(4-cyano-2-methylphenyl)sulfonyl]-2-methyl-1-piperazinecarboxylateHCID 59152098104.2%

Reaction Steps

To a solution of 1,1-dimethylethyl (2S)-2-methyl-1-piperazinecarboxylate (2.79 g, 13.91 mmol, supplier Antlantic Scitech) in DCM (80 mL), DIPEA (3.64 mL, 20.87 mmol) was added under argon atmosphere at room temperature then 4-cyano-2-methylbenzenesulfonyl chloride (3 g, 13.91 mmol) was added at 0° C. The ice bath was removed and the reaction mixture was stirred overnight. The reaction mixture was partitioned between DCM (30 ml) and aqueous sodium bicarbonate (2×20 ml). The organic phase was washed with HCl (2×20 ml) and water (2×20 ml) then it was dried (phase separator) and concentrated under vacuum to give the title compound (5.5 g) as a yellow viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697703B2
Source datasetuspto-grants-2014_04
ORD IDord-40483658d8bd4ead9776bf6f2bc44866
Source noteuspto-grants-2014_04