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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 850515생성일: 2026년 10월 26일

Sodium Bicarbonate → 1-(6-methoxy-5-pentyloxy-3,4-dihydro-1H-isoquinolin-2-yl)-2-(4-nitrophenyl)ethanone

https://huagongshe.com/reaction/850515

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물(4-Nitrophenyl)acetateHCID 6931101—
반응물6-Methoxy-5-pentyloxy-1,2,3,4-tetrahydroisoquinolineHCID 19363320—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-(6-methoxy-5-pentyloxy-3,4-dihydro-1H-isoquinolin-2-yl)-2-(4-nitrophenyl)ethanoneHCID 19363304—

반응 단계

6-Methoxy-5-pentyloxy-1,2,3,4-tetrahydroisoquinoline (116 mg, 0.465 mmol), (4-nitrophenyl)acetate (101.1 mg, 0.558 mmol) and 1-hydroxybenzotriazol hydrate (81.7 mg, 0.605 mmol) were dissolved in DMF (2 ml), and WSC hydrochloride (125 mg, 0.651 mmol) was added to this solution under ice-cooling. After stirring at room temperature for 3 hours, ethyl acetate (3 ml) and saturated aqueous sodium hydrogencarbonate solution (3 ml) were added to the reaction mixture to separate the organic layer. The organic layer was dried over anhydrous sodium sulfate. The drying agent was filtered off and the filtrate was concentrated under reduced pressure to give a crude product of 1-(6-methoxy-5-pentyloxy-3,4-dihydro-1H-isoquinolin-2-yl)-2-(4-nitrophenyl)ethanone. This product was used for the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06017919
출처 데이터셋uspto-grants-2000_01
ORD IDord-da005e14829e466da540592819bcca09
출처 메모uspto-grants-2000_01