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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694933Generated: November 1, 2026

1-(2-Chloro-5-fluorophenyl)-5,5-dimethylpiperazin-2-one → N-{(S)-2-[4-(2-Chloro-5-fluorophenyl)-2,2-dimethyl-5-oxopiperazin-1-yl]-1-[(2S,4S)-4-isopropyl-5-oxotetrahydrofuran-2-yl]ethyl}-2-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1694933

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Chloro-5-fluorophenyl)-5,5-dimethylpiperazin-2-oneHCID 66645399—
ReactantHCID 178448140HCID 178448140—
SolventTolueneHCID 1140—
ProductN-{(S)-2-[4-(2-Chloro-5-fluorophenyl)-2,2-dimethyl-5-oxopiperazin-1-yl]-1-[(2S,4S)-4-isopropyl-5-oxotetrahydrofuran-2-yl]ethyl}-2-nitrobenzenesulfonamideHCID 6664578391%

Reaction Steps

A solution of 1.15 g of (3S,5S)-3-isopropyl-5-[(S)-1-(2-nitrobenzenesulfonyl)aziridin-2-yl]dihydrofuran-2-one obtained in Example (1g) (3.25 mmol) and 889 mg of 1-(2-chloro-5-fluorophenyl)-5,5-dimethylpiperazin-2-one obtained in Example (62d) (3.9 mmol) in toluene (32 ml) was stirred at 110° C. for one hour. After cooling, the reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: toluene/acetone=10/1) to obtain 1.77 g of the title compound (yield: 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158790B2
Source datasetuspto-grants-2012_04
ORD IDord-e8e6c654c3234a268590099a9d9cd35d
Source noteuspto-grants-2012_04