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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154676Generated: October 26, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-(3-Chloropropyl)-3,4-dimethoxy-N-methylphenethylamineHCID 577693—
Reactant7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepin-2-oneHCID 11401769—
SolventDimethyl SulfoxideHCID 679—
Product1-[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—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490369
Source datasetuspto-grants-1984_12
ORD IDord-ad6624aec3ba45f5bf0598f0c6d817dc
Source noteuspto-grants-1984_12