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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397063생성일: 2026년 10월 24일

Triethylamine → 6-Methoxy-1-[1-(1-methyl-1H-imidazole-4-sulfonyl)-piperidin-4-yl]-3,4-dihydro-isoquinoline

https://huagongshe.com/ko/reaction/397063

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-methyl-1H-imidazole-4-sulfonyl chlorideHCID 2736887—
반응물6-Methoxy-1-piperidin-4-yl-3,4-dihydro-isoquinolineHCID 18172389—
용매DichloromethaneHCID 6344—
생성물6-Methoxy-1-[1-(1-methyl-1H-imidazole-4-sulfonyl)-piperidin-4-yl]-3,4-dihydro-isoquinolineHCID 1817246056.1%

반응 단계

To a stirred solution of 6-methoxy-1-piperidin-4-yl-3,4-dihydro-isoquinoline (0.094 g, 0.385 mmol) and triethylamine (0.078 g, 0.77 mmol) in CH2Cl2 (3 ml) was added 1-methyl-1H-imidazole-4-sulfonyl chloride (0.070 g, 0.385 mmol). The reaction mixture was stirred at RT under an atmosphere of N2 overnight. The reaction mixture was diluted with CH2Cl2 (10 ml) and washed with water (2×5 ml). The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified via radial chromatography (SiO2, 1 mm, CH2Cl2 to 5% MeOH/CH2Cl2) to give the product as an oil (0.084 g, 0.216 mmol, 56% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608203B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-88f163b020a4417a8afec3291f8f5e4c
출처 메모uspto-grants-2003_08