Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 216077생성일: 2026년 10월 25일
Lithium diisopropylamide → 1-tert-butyl 4-ethyl 4-((1-trityl-1H-imidazol-4-yl)methyl)piperidine-1,4-dicarboxylate
https://huagongshe.com/reaction/216077
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | 1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylate | HCID 2758812 | — |
| 반응물 | 4-(Chloromethyl)-1-trityl-1H-imidazole | HCID 2763176 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-tert-butyl 4-ethyl 4-((1-trityl-1H-imidazol-4-yl)methyl)piperidine-1,4-dicarboxylate | HCID 67037736 | 51% |
반응 단계
To a solution of 1-tert-butyl 4-ethyl piperidine-1,4-dicarboxylate (360 mg, 1.39 mmol) in anhydrous THF (10 mL) at −78° C. was added LDA (1.7 M in THF, 1.07 mL, 1.8 mmol) dropwise over 10 min. The reaction mixture was stirred at −78° C. for 1 hour, and 4-(chloromethyl)-1-trityl-1H-imidazole (500 mg, 13.9 mmol) in THF (5 mL) was added slowly. The reaction mixture was allowed to warm to room temperature over 1 hour, quenched with sat. aq. NH4Cl (10 mL), and extracted with EtOAc (3×20 mL). The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum. Purification by silica gel chromatography (10-50% EtOAc:Hexanes) afforded the title compound (403 mg, 51%). MS (ES+) [M+H]+=580.3.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08193202B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-a686ec2fdb7548279e6c96c348001610 |
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| 출처 메모 | uspto-grants-2012_06 |
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