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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850511Generated: October 28, 2026

Ethanol → HCID 19363278, compound

https://huagongshe.com/reaction/850511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 54551452HCID 54551452—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventTolueneHCID 1140—
ProductHCID 19363278HCID 1936327863%

Reaction Steps

Ethyl {(4-Methoxy-2-nitro-3-pentyloxybenzoyl)-[2-(4-nitrophenyl)-ethyl]amino}acetate (70.0 mg, 0.135 mmol) and ethanol (2 ml) were mixed, and 10% palladium-carbon catalyst was added. The reaction mixture was stirred in a stream of hydrogen at room temperature for 10.5 hours, and then filtered. The filtrate was concentrated under reduced pressure. Toluene (10 ml) and p-toluene sulfonate monohydrate (1 mg, 0.0053 mmol) were added to the precipitated crude crystals, and the mixture was refluxed under heating for 3.5 hours. Ethyl acetate (20 ml) was added to this reaction mixture, and the organic layer was washed with saturated aqueous sodium hydrogencarbonate solution (5 ml) and saturated brine (5 ml) and dried over anhydrous magnesium sulfate. The drying agent was filtered off and the filtrate was concentrated under reduced pressure. The obtained residue was purified by column chromatography on silica gel (chloroform/methanol=10/1) to give 4-[2-(4-aminophenyl)ethyl]-8-methoxy-9-pentyloxy-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione (35 mg, 63% in 2 steps) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017919
Source datasetuspto-grants-2000_01
ORD IDord-9f406abaa711433793964fdd1ade6a85
Source noteuspto-grants-2000_01