Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1788079생성일: 2026년 10월 24일
1-(2-Methoxyphenyl)piperazine → 3-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/ko/reaction/1788079
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | tert-Butyl 3-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylate | HCID 22647269 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 3-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-piperidine-1-carboxylic acid tert-butyl ester | HCID 21303201 | — |
반응 단계
To a solution of 3-methanesulfonyloxymethyl-piperidine-1-carboxylic acid tert-butyl ester (11.06 g, 0.04 mol) in acetonitrile (180 mL) was added potassium carbonate (26 g, 0.19 mol) followed by 1-(2-methoxy-phenyl) piperazine (7.25 g, 0.04 mol). After completion of addition the reaction mixture was heated to reflux. After 12 h the reaction mixture was cooled down to room temperature and quenched with water. The aqueous layer was extracted with ethyl acetate (3×100 mL). The combined organic layers were dried over sodium sulfate and concentrated to yield an oil. This crude material was purified using silica gel chromatography (7:3:0.05 Hexane:EtOAc:2M NH3 in EtOH) to afford the desired compound in good yield (8.0 g, 55%). C22H35N3O3, LRMS (m/z)=390 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07511141B2 |
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| 출처 데이터셋 | uspto-grants-2009_03 |
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| ORD ID | ord-987342903f5641e0bac10390d6fc29ed |
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| 출처 메모 | uspto-grants-2009_03 |
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