Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 567669생성일: 2026년 10월 25일
Triethylamine → (4S,2R,3R,5R)-2-{6-amino-2-[3-(2-phenylphenoxy)prop-1-ynyl]purin-9-yl}-5-(hydroxymethyl)oxolane-3,4-diol
https://huagongshe.com/reaction/567669
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | (Prop-2-ynyloxy)benzene | HCID 83613 | — |
| 반응물 | 2-Iodoadenosine | HCID 169662 | — |
| 촉매 | Copper iodide | HCID 83717 | — |
| 촉매 | HCID 178418476 | HCID 178418476 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (4S,2R,3R,5R)-2-{6-amino-2-[3-(2-phenylphenoxy)prop-1-ynyl]purin-9-yl}-5-(hydroxymethyl)oxolane-3,4-diol | HCID 9804898 | 38.1% |
반응 단계
To a solution of (4S,2R,3R,5R)-2-(6-amino-2-iodopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol (compound 1) (50 mg, 0.126 mmol) and prop-2-ynyloxybenzene (22 δ, 0.1605 mmol) in N,N-dimethylformamide (1 ml) and triethylamine (21 δ, 16.065 mmol) at 23° C. was added copper iodide (5 mg, 0.026 mmol) and dichlorobis(triphenylphosphine)palladium(II) (22 mg, 0.031 mmol) catalyst. After being stirred in a sealed reacti-vial at 80 C for 6 hours, the reaction was concentrated in vacuo, the residue purified by preparatory thin layer chromatography (methylene chloride:methanol 9:1) to afford compound 10 (9.6 mg, 0.024 mmol) in 20% yield. 1H NMR(CDCl3:CD3OD 9:1) δ 3.02-3.04 (m, 1H), 3.07 (s, 1H), 3.55, 3.74 (dd, 2H), 4.02 (s, 1H), 4.11-4.13 (m, 1H), 4.48-4.52 (m, 1H), 4.72 (s, 2H), 5.65 (d, 1H), 6.75-6.82 (m, 3H), 7.08-7.12 (m, 2H), 7.94 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06180615B2 |
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| 출처 데이터셋 | uspto-grants-2001_01 |
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| ORD ID | ord-0509b07fb38a469eb0d4cf0dd4648434 |
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| 출처 메모 | uspto-grants-2001_01 |
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