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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1154676생성일: 2026년 10월 27일

Water → 1-[7,8-Dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-methyl-N-(2-{3,4-dimethoxy-phenyl}-ethyl)-amino]-propane-dihydrochloride

https://huagongshe.com/reaction/1154676

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물N-(3-Chloropropyl)-3,4-dimethoxy-N-methylphenethylamineHCID 577693—
반응물7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepin-2-oneHCID 11401769—
용매Dimethyl SulfoxideHCID 679—
생성물1-[7,8-Dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-methyl-N-(2-{3,4-dimethoxy-phenyl}-ethyl)-amino]-propane-dihydrochlorideHCID 20433685—

반응 단계

1.1 gm (5.0 mmols) of 7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one were suspended in 20 ml of dimethyl sulfoxide, and the suspension was mixed with 0.6 gm (5.3 mmols) of potassium tert. butylate while stirring. After 10 minutes, the solution was mixed with 2.0 gm (7.4 mmols) of 1-chloro-3-[N-methyl-N-(2-{3,4-dimethoxy-phenyl}-ethyl)-amino]-propane; the mixture was stirred for one hour at 50° C. and then poured into water; the aqueous mixture was extracted with ethyl acetate, and the organic phase was evaporated in vacuo. The residue was purified on silica gel with methylene chloride +10% of methanol as the eluant, and the dihydrochloride was precipitated from acetone with ethereal hydrochloric acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04490369
출처 데이터셋uspto-grants-1984_12
ORD IDord-ad6624aec3ba45f5bf0598f0c6d817dc
출처 메모uspto-grants-1984_12