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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291553Generated: October 30, 2026

Sodium Iodide → HCID 18917235, compound

https://huagongshe.com/reaction/1291553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-MethylpiperazineHCID 53167—
Reactant5-[2-(p-Toluenesulfonyloxy)ethoxy]-7-fluoro-1-[2-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepineHCID 18917176—
SolventDimethylformamideHCID 6228—
ProductHCID 18917235HCID 18917235—

Reaction Steps

In 10 ml of dimethylformamide were dispersed 0.4 g of 5-[2-(p-toluenesulfonyloxy)ethoxy]-7-fluoro-1-[2-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepine, 0.38 ml of N-methylpiperazine and 0.3 g of sodium iodide. The dispersion was stirred at room temperature for 3 days. The reaction mixture was concentrated. The residue was mixed with water and the mixture was subjected to extraction with ethyl acetate. The extract was dried over sodium carbonate and purified by silica gel column chromatography (elutant: dichloromethane/-methanol=10/1) to obtain 1.15 g of 5-[2-(4-methyl-1-piperazinyl)ethoxy]-7-fluoro-1-[2-methoxy-4-(2-methyl-benzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepine. Colorless and amorphous

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753644
Source datasetuspto-grants-1998_05
ORD IDord-8873173aa6ec49b0b5c5b0a7b06292d3
Source noteuspto-grants-1998_05