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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 661572생성일: 2026년 10월 25일

2-Iodoquinoline → 4-(Hydroxy-quinolin-2-yl-methyl)-4-propyl-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/661572

반응식

참여 물질

역할이름HCID투입량
반응물2-IodoquinolineHCID 81044—
반응물Tert-butyl 4-formyl-4-propylpiperidine-1-carboxylateHCID 58017246—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물4-(Hydroxy-quinolin-2-yl-methyl)-4-propyl-piperidine-1-carboxylic acid tert-butyl esterHCID 5801728819%

반응 조건

온도0 °C

반응 단계

To a solution of 2-iodoquinoline (670 mg, 2.6 mmol) in THF (10 mL) at 0° C. was slowly added isopropyl magnesium chloride (2.0 M in THF, 1.6 mL, 3.2 mmol). The reaction mixture was stirred at 0° C. for 30 minutes, then a solution of 4-formyl-4-propyl-piperidine-1-carboxylic acid tert-butyl ester (670 mg, 2.6 mmol) in THF (3 mL) was slowly added. The reaction mixture was stirred at 0° C. for 30 minutes, then warmed to room temperature, quenched with saturated aqueous NH4Cl solution, and extracted with EtOAc. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (0% to 20% EtOAc in hexanes) to afford 190 mg (19%) of 4-(hydroxy-quinolin-2-yl-methyl)-4-propyl-piperidine-1-carboxylic acid tert-butyl ester as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08084623B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-c9201f90e68042faa3104c7b9bfe720a
출처 메모uspto-grants-2011_12