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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22819생성일: 2026년 10월 24일

Ethyl Acetate → 1-[7-(6-Chloro-indole-1-sulfonyl)-4,4-dimethyl-3,4-dihydro-1H-isoquinolin-2-yl]-ethanone

https://huagongshe.com/ko/reaction/22819

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물6-ChloroindoleHCID 87111—
반응물2-Acetyl-4,4-dimethyl-1,2,3,4-tetrahydro-isoquinoline-7-sulfonyl ChlorideHCID 22592023—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-[7-(6-Chloro-indole-1-sulfonyl)-4,4-dimethyl-3,4-dihydro-1H-isoquinolin-2-yl]-ethanoneHCID 2259202651%

반응 단계

Potassium tert-butoxide (37 mg, 0.33 mmol) was added to a stirred solution of 6-chloroindole (50 mg, 0.33 mmol) in dry tetrahydrofuran (1 ml) under argon at room temperature. After stirring for 5 minutes, a solution of 2-acetyl-4,4-dimethyl-1,2,3,4-tetrahydro-isoquinoline-7-sulfonyl chloride (D3) (100 mg, 0.33 mmol) in dry tetrahydrofuran (1 ml) was added and the solution was stirred for a further 3 h. Ethyl acetate (5 ml) and water (5 ml) were added to the reaction mixture, which was then shaken. The layers were separated and the organic phase was washed with brine (5 ml), dried (MgSO4) and concentrated in vacuo to an oil. The oil was purified by column chromatography over silica gel eluting with a gradient of acetone/toluene to afford the title compound (D4) (70 mg, 51%), MS: m/z (MH+) 417/419.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849644B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-a915c780e31247d2aa26832773c9cdd8
출처 메모uspto-grants-2005_02