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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

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylateHCID 2776270—
반응물2-Benzyl-4-methoxy-N-methylbenzamideHCID 22555927—
반응물Isopropanol carbon dioxideHCID 86586944—
반응물CID 53628100HCID 178418400—
용매TetrahydrofuranHCID 8028—
용매Ethyl acetate hexaneHCID 21226206—
생성물Benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylateHCID 6843349049.4%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741322B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-cdf90ed4d8804be8853d1f11965f5421
출처 메모uspto-grants-2010_06