Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 745생성일: 2026년 10월 23일
Ethyl 4-piperidinecarboxylate → Ethyl 1-(4-(tert-butoxycarbonyl)phenyl)piperidine-4-carboxylate
https://huagongshe.com/ko/reaction/745
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| 반응물 | Tert-butyl 4-bromobenzoate | HCID 11334366 | — |
| 시약 | Cesium carbonate | HCID 10796 | — |
| 촉매 | Binap, (A+-)- | HCID 634876 | — |
| 촉매 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | Ethyl 1-(4-(tert-butoxycarbonyl)phenyl)piperidine-4-carboxylate | HCID 19063865 | 0% |
반응 단계
1\. To a microwave tube was added tert-butyl 4-bromobenzoate (1.328 g, 5.16 mmol), ethyl piperidine-4-carboxylate (1.000 g, 5.16 mmol), Cs2CO3 (5.05 g, 15.49 mmol), Pd2dba3 (0.473 g, 0.52 mmol), and BINAP (0.643 g, 1.03 mmol). The mixture was dissolved in [Solvents] and sealed. The tube was de-gassed and inflated with N2. 2\. The reaction was heated at 110°C in oil-bath overnight. LCMS showed reaction complete. The reaction mixture was filter through celite pad and the solution was loaded to column for a ISCO purification (30% EtOAc in Hex). The purification is difficult with multiple by-products. Several ISCO purification was carried out and fractions were combined with other batches. Yield was poor.
출처 및 근거
| 출처 데이터셋 | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-1beac9199051463f81c658e8f7cb9a0d |
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| 출처 메모 | 750 AstraZeneca ELN dataset |
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