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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1864363생성일: 2026년 10월 27일

1-(2,5-Xylyl)piperazine → (RS)-4-[4-(2,5-dimethyl-phenyl)-piperazine-1-carbonyl]-1-(3-methoxy-benzenesulfonyl)-3-phenyl-imidazolidin-2-one

https://huagongshe.com/reaction/1864363

반응식

참여 물질

역할이름HCID투입량
반응물1-(2,5-Xylyl)piperazineHCID 70542—
반응물DiisopropylethylamineHCID 81531—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물(RS)-1-(3-methoxy-benzenesulfonyl)-2-oxo-3-phenyl-imidazolidine-4-carboxylic acidHCID 67141122—
용매TetrahydrofuranHCID 8028—
생성물(RS)-4-[4-(2,5-dimethyl-phenyl)-piperazine-1-carbonyl]-1-(3-methoxy-benzenesulfonyl)-3-phenyl-imidazolidin-2-oneHCID 25027492111.5%

반응 단계

To a solution of (RS)-1-(3-methoxy-benzenesulfonyl)-2-oxo-3-phenyl-imidazolidine-4-carboxylic acid (0.040 g) in tetrahydrofuran (2 ml) were added 1-(2,5-dimethylphenyl)-piperazine (0.030 g), (benzotriazol-1-yloxy)-tris-(dimethylamino)-phosphonium-hexafluorophosphate (BOP reagent, 0.071 g) and N-ethyl-diisopropylamine (0.041 g). The mixture was stirred at room temperature for 4 h. The solvent was evaporated and the product was purified by chromatography (SiO2, cyclohexane/ethyl acetate 4:1=>1:1) to give (RS)-4-[4-(2,5-dimethyl-phenyl)-piperazine-1-carbonyl]-1-(3-methoxy-benzenesulfonyl)-3-phenyl-imidazolidin-2-one (0.065 g) as a colorless solid. MS: 549.0 ([M+H]+)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07625902B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-750c04ce3ecf4b1abac3bc9f73f772a1
출처 메모uspto-grants-2009_12