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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

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Methoxyphenyl)piperazineHCID 1346—
반응물Potassium CarbonateHCID 11430—
반응물tert-Butyl 3-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylateHCID 22647269—
용매AcetonitrileHCID 6342—
생성물3-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07511141B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-987342903f5641e0bac10390d6fc29ed
출처 메모uspto-grants-2009_03