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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

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참여 물질

역할이름HCID투입량
반응물Lithium diisopropylamideHCID 2724682—
반응물1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylateHCID 2758812—
반응물4-(Chloromethyl)-1-trityl-1H-imidazoleHCID 2763176—
용매TetrahydrofuranHCID 8028—
생성물1-tert-butyl 4-ethyl 4-((1-trityl-1H-imidazol-4-yl)methyl)piperidine-1,4-dicarboxylateHCID 6703773651%

반응 조건

온도-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193202B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a686ec2fdb7548279e6c96c348001610
출처 메모uspto-grants-2012_06