Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1501997생성일: 2026년 10월 27일
tert-Butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylate → tert-butyl (3R)-4-[2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl]-3-(hydroxymethyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1501997
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | tert-Butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylate | HCID 24820286 | — |
| 반응물 | 6-Fluoro-2-methyl-3-(oxiran-2-yl)benzonitrile | HCID 86647307 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | tert-butyl (3R)-4-[2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl]-3-(hydroxymethyl)piperazine-1-carboxylate | HCID 86727051 | — |
반응 단계
6-Fluoro-2-methyl-3-(2-oxiranyl)benzonitrile (prepared as described above, 4.80 g, 27.1 mmol) and (R)-4-N—BOC-2-hydroxymethyl-piperazine (8.79 g. 40.6 mmol) were suspended in EtOH (30 mL) and heated in a microwave apparatus at 150° C. for 1 h. The reaction mixture was cooled and evaporated to dryness. The residue was purified by chromatography through a 330 g ISCO Redi-sep column eluting with ethyl acetate to 5% MeOH/ethyl acetate to yield the title compound. LC-MS: M+1=394;
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-b2ced58ff72742338b806967d6069cd0 |
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| 출처 메모 | uspto-grants-2015_12 |
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