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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1363982생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1363982

반응식

참여 물질

역할이름HCID투입량
반응물2-IodoadenosineHCID 169662—
반응물2-Methoxyphenyl 4-(prop-2-ynyl)piperidine-1-carboxylateHCID 57838876—
생성물2-{3-[1-((2-Methoxy)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosineHCID 25094184—

반응 단계

2-Methoxyphenyl 4-(prop-2-ynyl)piperidine-1-carboxylate (0.565 g, 2.067 mmol) was added to a solution of 2-iodoadenosine (0.650 g, 1.653 mmol) according to general procedure 2: yield 775 mg, 87%. 1H NMR (CD3OD) δ 8.30 (s, 1H), 7.24-7.17, 7.09-7.04, 6.97-6.91 (3×m, 4H), 5.96 (d, 1H, J=6.5 Hz), 4.74 (dd, 1H, J=5.1, J=6.4 Hz), 4.43-4.32 (m, 2H), 4.25-4.16 (m, 2H), 3.96-3.89, 3.82 (s, 3H), 3.80-3.74, (2×m, 2H), 3.07, 2.92 (2×br t, 2H), 2.51 (d, 2H, J=6.0 Hz), 2.03-1.85, 1.60-1.35 (2×m, 5H). 13C NMR (CD3OD) δ 157.3, 155.5, 153.1, 150.2, 147.5, 142.6, 141.9, 127.6, 124.1, 121.7, 120.4, 113.7, 91.3, 88.3, 86.7, 82.2, 75.5, 72.6, 64.7, 63.5, 56.4, 45.8, 36.6, 32.5, 26.5, 25.2. LRMS ESI (M+H+) 539.1. HPLC rt=5.1 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07888329B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-25fb55b8a35549c9908860b37dd5dc59
출처 메모uspto-grants-2011_02