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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 751169생성일: 2026년 10월 26일

Cesium carbonate → (2S,3S)-1-tert-Butyloxycarbonyl-3-(tert-butyldimethylsilanyloxy)-2-[(1R)-1-(3-chloro-4-cyano-2-methylphenylamino)ethyl]pyrrolidine

https://huagongshe.com/reaction/751169

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Chloro-4-iodo-3-methylbenzonitrileHCID 16731995—
반응물(2S,3S)-N-tert-Butyloxycarbonyl-3-(tert-butyldimethylsilanyloxy)-2-((1R)-1-aminoethyl)pyrrolidineHCID 68457944—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매(S)-(R)-PpfaHCID 44630263—
용매TolueneHCID 1140—
생성물(2S,3S)-1-tert-Butyloxycarbonyl-3-(tert-butyldimethylsilanyloxy)-2-[(1R)-1-(3-chloro-4-cyano-2-methylphenylamino)ethyl]pyrrolidineHCID 6845955418.2%

반응 조건

온도140 °C

반응 단계

To a solution of 80D (137 mg, 0.40 mmol) in nitrogen degassed toluene (3 mL) at rt was added 2-chloro-4-iodo-3-methyl-benzonitrile (122 mg, 0.44 mmol), Cs2CO3 (260 mg, 0.80 mmol) and Pd2(dba)3 (7.3 mg, 0.008 mmol) and (S)-N,N-dimethyl-1-[(R)-2-(diphenyphosphino)ferrocenyl]ethylamine (11 mg, 0.024 mmol). The reaction was degassed with nitrogen for 30 min, sealed and heated at 140° C. for 2 h under microwave conditions. The mixture was cool to rt, diluted with hexane and filtered through a layer of celite. The filtrate was evaporated to give the crude product. Purification by flash chromatography (10 g ISCO silica gel cartridge, 0-20% EtOAc in hexane gradient) gave the title compound 80E (36 mg): MS (ES) m/z 345 [M+H]+; HRMS calcd for C25H41N3O3ClSi 494.2606, found 494.2606.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07405234B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-d8513e16568e410f9958a900f9e5264a
출처 메모uspto-grants-2008_07