Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5546생성일: 2026년 10월 23일
(Z)-Tri-n-butyl(1-propenyl)tin → Diphenylmethyl 7-Phenoxyacetamido-3-(Z-1-propenyl)-3-cephem-4carboxylate
https://huagongshe.com/ko/reaction/5546
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (Z)-Tri-n-butyl(1-propenyl)tin | HCID 10914524 | — |
| 반응물 | Diphenylmethyl 7-Phenoxyacetamido-3-[(fluorosulfonyl)oxy]-3-cephem-4-carboxylate | HCID 88424184 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Diphenylmethyl 7-Phenoxyacetamido-3-(Z-1-propenyl)-3-cephem-4carboxylate | HCID 14608940 | 92.9% |
반응 단계
A solution of palladium (II) acetate (3.6 mg, 0.016 mmole, 0.1 eq.) in dichloromethane (2 mL) was treated with Z-1-propenyl tri-n-butylstannane (66.2 mg, 0.2 mmole, 1.2 eq.) under an inert atmosphere and allowed to stir for 3 minutes. The resulting dark suspension was then treated with diphenylmethyl 7-phenoxyacetamido-3-[(fluorosulfonyl) oxy]-3-cephem-4-carboxylate (100.0 mg, 0.16 mmole, 1.0 eq.) in one portion and the reaction mixture was allowed to stir for 10 minutes. The reaction mixture was diluted with additional dichloromethane and washed with water (1×10 mL). The organic fraction was dried over magnesium sulfate and purified by flash filtration through a pad of silica gel (W. R. Grace, 951W) first with dichloromethane (50 mL) to remove the residual stannane and then with 10% ethyl acetate in dichloromethane (50 mL) which upon concentration furnished 80.4 mg (89%) of the title compound as a pale yellow solid. The product was then recrystallized from isopropyl alcohol to afford 62.3 mg (69%) of a white solid, mp. 103°-104° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05245027 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-c2b21fff05b941f38cbaf9f020481d88 |
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| 출처 메모 | uspto-grants-1993_09 |
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