Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
tert-Butyl 4-oxopiperidine-1-carboxylate → 5-Tert-butyl 2-ethyl 6,7-dihydro-1H-pyrrolo[3,2-C]pyridine-2,5(4H)-dicarboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | Bromoethyl pyruvate | HCID 86587973 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Tert-butyl 2-ethyl 6,7-dihydro-1H-pyrrolo[3,2-C]pyridine-2,5(4H)-dicarboxylate | HCID 66864309 | — |
반응 단계
A solution of N-boc-4-piperidone (1 eq.) and lithium di-isopropyl amide (1 eq.) in THF was stirred at −78° C. and for 2 hrs. A bromoethyl pyruvate (1.2 eq.) was added to above reaction mixture and stirred for 30 min. Reaction mixture was then quenched with ammonia solution and then extracted with ethyl acetate, dried over sodium sulphate and concentrated to dryness. The residue was then dissolved in dichoromethane and was added silica (100-200 mesh), stirred for overnight at room temperature. Crude was then purified by silica gel column chromatography to yield 5-tert-butyl 2-ethyl 1,4,6,7-tetrahydro-5H-pyrrolo[3,2-c]pyridine-2,5-dicarboxylate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08440830B2 |
| 출처 데이터셋 | uspto-grants-2013_05 |
| ORD ID | ord-6f708db8a9684e74b0489fe18c279fe5 |
| 출처 메모 | uspto-grants-2013_05 |