Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17871생성일: 2026년 10월 23일
Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylate → Benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate
https://huagongshe.com/ko/reaction/17871
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylate | HCID 2776270 | — |
| 반응물 | 2-Benzyl-4-methoxy-N-methylbenzamide | HCID 22555927 | — |
| 반응물 | Isopropanol carbon dioxide | HCID 86586944 | — |
| 반응물 | CID 53628100 | HCID 178418400 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl acetate hexane | HCID 21226206 | — |
| 생성물 | Benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate | HCID 68433490 | 49.4% |
반응 단계
To an isopropanol/dry ice cooled solution of 4-Methoxy-N-methyl-2-(phenylmethyl)benzamide (250 mg, 0.980 mmol) in THF (50 mL) under argon was added sec-butyllithium solution (1.3M, 1.55 mL, 2.00 mmol) dropwise. After 10 min. a THF (10 mL) solution of benzyl-4-(chlorocarbonyl)piperidine-1-carboxylate (275 mg, 980 mmol) was quickly added to the reaction solution. After 10 min. the reaction was quenched with water then warmed to room temperature. Saturated sodium bicarbonate was added and the resulting mixture extracted with ethyl acetate (3×) and dried with anhydrous magnesium sulfate. Filtration followed by evaporation of solvent in vacuo gave the crude product which was subjected to flash column chromatography (hexane:ethyl acetate 50:50) to afford benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate as a white foam (242 mg, 0.484 mmol, 49%). MS [M+H]+ 501.2
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07741322B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-cdf90ed4d8804be8853d1f11965f5421 |
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| 출처 메모 | uspto-grants-2010_06 |
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