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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-Iodoquinoline | HCID 81044 | — |
| 반응물 | Tert-butyl 4-formyl-4-propylpiperidine-1-carboxylate | HCID 58017246 | — |
| 반응물 | HCID 178418918 | HCID 178418918 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-(Hydroxy-quinolin-2-yl-methyl)-4-propyl-piperidine-1-carboxylic acid tert-butyl ester | HCID 58017288 | 19% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08084623B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-c9201f90e68042faa3104c7b9bfe720a |
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| 출처 메모 | uspto-grants-2011_12 |
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