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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154644Generated: November 2, 2026

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

https://huagongshe.com/reaction/1154644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant1-[7,8-Dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-methyl-N-(2-{4-amino-3,5-dichloro-phenyl}-ethyl)-amino]-propaneHCID 13316678—
SolventChloroformHCID 6212—
Product1-[7,8-Dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-methyl-N-(2-{4-acetylamino-3,5-dichloro-phenyl}-ethyl)-amino]-propaneHCID 20433837—

Reaction Steps

A solution of 3 gm (0.0063 mol) of 1-[7,8-dimethoxy-1,3,4,5,-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-methyl-N-(2-{4amino-3,5-dichloro-phenyl}ethyl)-amino]-propane in 50 ml of chloroform and 0.7 gm (0.007 mol) of triethylamine was mixed at the boiling point in portions with altogether about 0.8 ml of acetyl chloride. After boiling it for several hours, the reaction mixture was cooled to room temperature and washed with water. The aqueous phase was made strongly alkaline with 2N sodium hydroxide and extracted with methylene chloride. The separated organic phase was dried over sodium sulfate and evaporated. The crude product thus obtained was purified by chromatography on silica gel (particle size: 0.063 to 0.2 mm, eluant: methylene chloride/methanol=8:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490369
Source datasetuspto-grants-1984_12
ORD IDord-9187d780c62e4130a550bbb55068b081
Source noteuspto-grants-1984_12