Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239651생성일: 2026년 10월 25일
Dichloromethane → 2-((4-amino-3-(3-hydroxyprop-1-ynyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-phenyl-4H-chromen-4-one
https://huagongshe.com/reaction/239651
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Propargyl alcohol | HCID 7859 | — |
| 반응물 | 2-((4-Amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-phenyl-4H-chromen-4-one | HCID 58269147 | — |
| 촉매 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-((4-amino-3-(3-hydroxyprop-1-ynyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-phenyl-4H-chromen-4-one | HCID 58269160 | 77% |
반응 단계
To a solution of Example 57a (0.180 g, 0.363 mmoles) in THF (5 ml), propargyl alcohol (0.051 g, 0.436 mmoles) diisopropylamine (0.31 ml, 1.81 mmoles), copper(I) iodide (7 mg, 0.036 mmoles) and) Tetrakis triphenylphosphine Palladium (0.042 g, 0.0363 mmoles) were added and the system is degassed for 30 min. and heated to reflux for 4 h. The reaction mixture filtered through celite pad and washed with ethyl acetate. The filtrate was dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by column chromatography with methanol: dichloromethane to afford the title compound as brown solid (0.118 g, 77% yield). MP: 171-173° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 8.21(s, 1H), 8.06(dd, J=7.9, 1.6 Hz, 1H), 7.77(m, 1H), 7.50(dt, J=8.0, 0.9 Hz, 1H), 7.40-7.33(m, 6H), 5.43(s, 2H), 4.33(d, J=6.1 z, 2H). Mass: 423.88(M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642607B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-87b0b3990f124371a1847315acfb2693 |
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| 출처 메모 | uspto-grants-2014_02 |
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