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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397064생성일: 2026년 10월 24일

Sodium borohydride → 6-Methoxy-1-[1-(1-methyl-1H-imidazole-4-sulfonyl)-piperidin-4-yl]-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/ko/reaction/397064

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물6-Methoxy-1-[1-(1-methyl-1H-imidazole-4-sulfonyl)-piperidin-4-yl]-3,4-dihydro-isoquinolineHCID 18172460—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Sodium BicarbonateHCID 516892—
생성물6-Methoxy-1-[1-(1-methyl-1H-imidazole-4-sulfonyl)-piperidin-4-yl]-1,2,3,4-tetrahydroisoquinolineHCID 1817242971.6%

반응 단계

To a stirred solution of 6-methoxy-1-[1-(1-methyl-1H-imidazole-4-sulfonyl)-piperidin-4-yl]-3,4-dihydro-isoquinoline (0.077 g, 0.197 mmol) in MeOH (3 ml) cooled to 0° C. was added NaBH4. The reaction mixture was then stirred at RT for 2 hours and diluted with water (5 ml) and sat. NaHCO3 (5 ml). The mixture was extracted with EtOAc (3×10 ml). The combined organics were washed with brine (1×10 ml), dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by radial chromatography (SiO2, 1 mm, CH2Cl2 to 5% MeOH/CH2Cl2) to give the product as an oil (0.055 g, 0.141 mmol, 71% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608203B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-44e81755739f48caaea3a7be78b51332
출처 메모uspto-grants-2003_08