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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694979Generated: November 1, 2026

5,5-Dimethyl-1-(5-fluoro-2-methylphenyl)piperazin-2-one → N-{(S)-2-[2,2-Dimethyl-4-(5-fluoro-2-methylphenyl)-5-oxopiperazin-1-yl]-1-[(2S,4R)-4-methyl-5-oxotetrahydrofuran-2-yl]ethyl}-2-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1694979

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,5-Dimethyl-1-(5-fluoro-2-methylphenyl)piperazin-2-oneHCID 66645745—
ReactantHCID 178461437HCID 178461437—
SolventTolueneHCID 1140—
ProductN-{(S)-2-[2,2-Dimethyl-4-(5-fluoro-2-methylphenyl)-5-oxopiperazin-1-yl]-1-[(2S,4R)-4-methyl-5-oxotetrahydrofuran-2-yl]ethyl}-2-nitrobenzenesulfonamideHCID 6664555895.4%

Reaction Steps

A solution of 844 mg of (3R,5S)-3-methyl-5-[(S)-1-(2-nitrobenzenesulfonyl)aziridin-2-yl]dihydrofuran-2-one obtained in Example (76g) (2.59 mmol) and 733 mg of 5,5-dimethyl-1-(5-fluoro-2-methylphenyl)piperazin-2-one obtained in Example (70d) (3.10 mmol) in toluene (26 ml) was stirred at 110° C. for two hours. After cooling, the reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent:methylene chloride/ethyl acetate=3/1-1/1) to obtain 1.39 g of the title compound (yield: 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158790B2
Source datasetuspto-grants-2012_04
ORD IDord-aea4ac50093c4fe3827d7b121b1c3f9a
Source noteuspto-grants-2012_04