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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate | HCID 24820294 | — |
| 반응물 | 5-(oxiran-2-yl)-2-benzofuran-1(3H)-one | HCID 59568715 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | tert-butyl(3S)-3-(hydroxymethyl)-4-[2-hydroxy-2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate | HCID 71271745 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09206199B2 |
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| 출처 데이터셋 | uspto-grants-2015_12 |
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| ORD ID | ord-46dab300aa3e4aba998386750e6c0722 |
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| 출처 메모 | uspto-grants-2015_12 |
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