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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 475418생성일: 2026년 10월 24일

3-Amino-1-adamantanol → (2S,5R)-5-ethynyl-1-{N-((5R,7S)-3-hydroxy-1-adamantyl)glycyl}pyrrolidine-2-carbonitrile

https://huagongshe.com/ko/reaction/475418

반응식

참여 물질

역할이름HCID투입량
반응물3-Amino-1-adamantanolHCID 658645—
반응물(2S,5R)-1-(2-chloroacetyl)-5-ethynylpyrrolidine-2-carbonitrileHCID 16090854—
용매AcetonitrileHCID 6342—
생성물(2S,5R)-5-ethynyl-1-{N-((5R,7S)-3-hydroxy-1-adamantyl)glycyl}pyrrolidine-2-carbonitrileHCID 9973731—

반응 단계

To a stirred solution of Example 8D (0.06 g, 0.305 mmol) in acetonitrile (3 mL) at room temperature under nitrogen, was added 3-amino-1-adamantanol (0.1 g, 0.61 mmol). The reaction mixture was stirred for two days and then concentrated under reduced pressure. The residue was flash chromatographed with 5-7% MeOH/CH2Cl2 to provide the desired compound as a pale yellow oil. MS (DCI) m/z 328 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 1.5-2 (14H, m), 2.11-2.21 (2H, m), 2.45-2.48 (2H, m), 3.78 (1H, d), 3.8-4.5 (2H, m), 4.53-4.55 (1H, t), 5.01 (1H, m), 5.05 (1H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637546B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-21d2c4ca7bf24e40993f1ab7b71b048f
출처 메모uspto-grants-2014_01