Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60734생성일: 2026년 10월 24일
Azobisisobutyronitrile → 1-[(2S,4R,5R)-4-allyl-5-(5-amino-2,7-dioxo-6H-thiazolo[4,5-d]pyrimidin-3-yl)tetrahydrofuran-2-yl]propyl benzoate
https://huagongshe.com/ko/reaction/60734
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Azobisisobutyronitrile | HCID 6547 | — |
| 반응물 | Allyltributylstannane | HCID 90628 | — |
| 반응물 | 1-[(2S,4R,5R)-5-(5-amino-2,7-dioxo-6H-thiazolo[4,5-d]pyrimidin-3-yl)-4-phenoxycarbothioyloxy-tetrahydrofuran-2-yl]propyl benzoate | HCID 137108742 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 1-[(2S,4R,5R)-4-allyl-5-(5-amino-2,7-dioxo-6H-thiazolo[4,5-d]pyrimidin-3-yl)tetrahydrofuran-2-yl]propyl benzoate | HCID 137108717 | 179.6% |
반응 단계
A mixture of 1-[(2S,4R,5R)-5-(5-amino-2,7-dioxo-6H-thiazolo[4,5-d]pyrimidin-3-yl)-4-phenoxycarbothioyloxy-tetrahydrofuran-2-yl]propyl benzoate (compound 26e, 1.14 g, 2.0 mmol), 2,2′-azobisisobutyronitrile (168 mg, 1 mmol) and allyl(tributyl)stannane (3.08 mL, 10 mmol) in anhydrous toluene (15 mL) was degassed with argon and then heated with stirring at 80° C. for 4 hours. The resulting mixture was stirred with saturated aqueous NH4F at room temperature for 2 hours and extracted with DCM twice. The combined organic layers were dried over Na2SO4, concentrated in vacuo and the residue was purified by column chromatography on silica gel (eluting with 1:3 EtOAc in petroleum ether) to afford 820 mg of 1-[(2S,4R,5R)-4-allyl-5-(5-amino-2,7-dioxo-6H-thiazolo[4,5-d]pyrimidin-3-yl)tetrahydrofuran-2-yl]propyl benzoate (compound 26f) as a brown solid. MS obsd. (ESI+) [(M+H)+]: 457.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09441008B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-5cdf030cb7194ab58cfd9dfc480e080c |
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| 출처 메모 | uspto-grants-2016_09 |
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