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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 497557생성일: 2026년 10월 23일

N,N-bis(2-chloroethyl)-p-toluenesulphonamide → Methyl (2S)-2-{4-[(4-methylphenyl)sulfonyl]-1-piperazinyl}-3-(1-trityl-1H-imidazol-4-yl)propanoate

https://huagongshe.com/ko/reaction/497557

반응식

참여 물질

역할이름HCID투입량
반응물N,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 96039—
반응물H-His(Trt)-OMeHCID 7408414—
용매AcetonitrileHCID 6342—
용매DiisopropylethylamineHCID 81531—
생성물Methyl (2S)-2-{4-[(4-methylphenyl)sulfonyl]-1-piperazinyl}-3-(1-trityl-1H-imidazol-4-yl)propanoateHCID 6003061219%

반응 단계

A suspension of methyl (2S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanoate (1 g, 2.4 mmol) in diisopropylethylamine (5 ml), was stirred at room temperature for 20 minutes. N,N-Bis(2-chloroethyl)-4-methylbenzenesulfonamide (720 mg, 2.4 mmol) was added and the mixture was stirred at reflux for 3 hours. The mixture was allowed to cool and diluted with acetonitrile. The resultant solution was concentrated under reduced pressure and the residue was suspended in aqueous sodium carbonate solution and extracted with dichloromethane (3×20 ml). The combined organic extracts were washed with brine (3×20 ml), dried (Na2SO4), filtered, and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with a solvent gradient of dichloromethane:methanol (99:1). The isolated material was dissolved in ether and the resultant solution concentrated under reduced pressure to afford the title compound as a colorless foam, 300 mg, 19% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06949577B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-eda09d4e0eff4cd9866ba262d47e0e6b
출처 메모uspto-grants-2005_09