Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097718생성일: 2026년 10월 27일
Triphenylphosphine → 3-Butyl-8-chloro-1-[4-(3-phenyl-5-isoxazolyl)butyl]-3,7-dihydro-1H-purine-2,6-dione
https://huagongshe.com/reaction/1097718
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylate | HCID 75557 | — |
| 반응물 | 3-butyl-8-chloro-7-(2-propen-1-yl)-3,7-dihydro-1H-purine-2,6-dione | HCID 59299582 | — |
| 반응물 | 4-(3-Phenyl-5-isoxazolyl)-1-butanol | HCID 59395604 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-Butyl-8-chloro-1-[4-(3-phenyl-5-isoxazolyl)butyl]-3,7-dihydro-1H-purine-2,6-dione | HCID 59395463 | 35.8% |
반응 단계
3-Butyl-8-chloro-7-(2-propen-1-yl)-3,7-dihydro-1H-purine-2,6-dione (100 mg, 0.354 mmol) and 4-(3-phenyl-5-isoxazolyl)-1-butanol (77 mg, 0.355 mmol) were dissolved in dry THF (4 ml) under nitrogen. A solution of dibenzyl azodicarboxylate (94%, 224 mg, 0.708 mmol) in dry THF (2 ml) was added. The mixture was cooled to 0° C. and a solution of triphenylphosphine (185 mg, 0.708 mmol) in dry THF (1 ml) was added. The mixture was stirred for 20 min at 0° C. then at room temperature overnight. The mixture was degassed then stirred with morpholine (0.308 ml) and tetrakis(triphenylphosphine)palladium(0) (82 mg) for 4.5 h. A further 60 mg of tetrakis(triphenylphosphine)palladium(0) was added and stirring continued overnight. The reaction was worked up by partition between EtOAc and 2M HCl, the organic phase evaporated and purified by aminopropyl SPE (5 g) washing with THF-MeOH (1:1), MeOH and eluting with DCM-MeOH (1:1) containing 5% AcOH. Further purification by MDAP afforded the title compound (56 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08143264B2 |
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| 출처 데이터셋 | uspto-grants-2012_03 |
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| ORD ID | ord-1b6ecf0713db43e3a1daa254858a9817 |
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| 출처 메모 | uspto-grants-2012_03 |
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