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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535089생성일: 2026년 10월 24일

Acetonitrile → Methyl (3r,4s)-1-[(z)-1-(methylthio)-2-nitrovinyl]-4-[(3r)-3-phenylpyrrolidin-1-yl]carbonylpiperidine-3-carboxylate

https://huagongshe.com/ko/reaction/535089

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참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물TriethylamineHCID 8471—
반응물1,1-Bis(methylthio)-2-nitroethyleneHCID 83623—
반응물(3r,4s)-4-((r)-3-Phenyl-pyrrolidine-1-carbonyl)-piperidine-3-carboxylic acid methyl esterHCID 67304902—
생성물Methyl (3r,4s)-1-[(z)-1-(methylthio)-2-nitrovinyl]-4-[(3r)-3-phenylpyrrolidin-1-yl]carbonylpiperidine-3-carboxylateHCID 6730456653.4%

반응 조건

온도85 °C

반응 단계

To a stirred solution of (3R,4S)-4-((R)-3-phenyl-pyrrolidine-1-carbonyl)-piperidine-3-carboxylic acid methyl ester (3.10E2 mg, 0.000980 mol) in anhydrous acetonitrile (9.8 mL, 0.19 mol) at rt was added triethylamine (274 uL, 0.00196 mol) and 1,1-bis(methylthio)-2-nitroethylene (248 mg, 0.00147 mol). The reaction mixture was heated to reflux (oil bath temperature: 85° C.) for 19 h. The reaction mixture was concentrated in vacuo. The residue was purified by Combiflash with 40-95% EtOAc/Hex to give the product as a yellow viscous oil (227 mg, 53% in yield). MS (ESI): (M+H)+=434.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853243B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-29da9d92aa9f44a8ae644a0d3bb384bc
출처 메모uspto-grants-2014_10