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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1501926생성일: 2026년 10월 25일

tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate → tert-butyl(3S)-3-(hydroxymethyl)-4-[2-hydroxy-2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/1501926

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820294—
반응물5-(oxiran-2-yl)-2-benzofuran-1(3H)-oneHCID 59568715—
용매EthanolHCID 702—
생성물tert-butyl(3S)-3-(hydroxymethyl)-4-[2-hydroxy-2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylateHCID 71271745—

반응 조건

온도150 °C

반응 단계

5-(Oxiran-2-yl)-2-benzofuran-1(3H)-one (1.5 g, 8.5 mmol) and commercially available (S)-4-N—BOC-2-hydroxymethyl piperazine (2.394 g, 11.07 mmol) were combined in ethanol (10 mL) in a microwave tube. The mixture was degassed then heated for 60 min at 150° C. LC-MS showed the product peak. The reaction was worked up by adding ethyl acetate and washing once with brine. The organic layer was separated, dried, and concentrated to dryness. The crude product was purified by MPLC using an 80 g Redi-sep column and eluted with 50%-100% EtOAc/hexane yielding the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09206199B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-46dab300aa3e4aba998386750e6c0722
출처 메모uspto-grants-2015_12