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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732904생성일: 2026년 10월 27일

2-Iodoadenosine → 2-{3-[1-((4-Nitrophenoxy)carbonyl)piperidin-4-yl]propyn-1-yl}adenosine

https://huagongshe.com/reaction/732904

반응식

참여 물질

역할이름HCID투입량
반응물2-IodoadenosineHCID 169662—
반응물4-Nitrophenyl 4-(prop-2-ynyl)piperidine-1-carboxylateHCID 57838889—
생성물2-{3-[1-((4-Nitrophenoxy)carbonyl)piperidin-4-yl]propyn-1-yl}adenosineHCID 25094106—

반응 단계

Batch: AB-9-149. 4-nitrophenyl 4-(prop-2-ynyl)piperidine-1-carboxylate, batch JR28-97 (0.630 g, 2.185 mmol) was added to a solution of 2-iodoadenosine (0.727 g, 1.849 mmol) according to general procedure 2. Yield: 1.192 g, 65%. %. 1H NMR (CD3OD) δ 8.26 (m, 1H), 8.25-7.34 (2×m, 4H), 5.94 (d, 1H), 4.72 (m, 2H), 4.32-4.14 (2×m, 3H), 3.91-3.71 (2×d, 2H), 3.17-2.90 (2×bt, 4H), 2.48 (d, 5H), 1.45 (m, 5H). m/z MH+=554.15. HPLC rt=7.3 mm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07589076B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-3dbfef74a8454c3194f1bfb421c4be68
출처 메모uspto-grants-2009_09