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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33220Generated: October 30, 2026

Ethylenediamine → 3-(tert-Butyloxycarbonyl)-7-(pyrazin-2-yl)-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/33220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantPotassium HydroxideHCID 14797—
ReactantSelenium DioxideHCID 24007—
Reactanttert-butyl 7-acetyl-2,3,4,5-tetrahydro-1H-3-benzazepine-3-carboxylateHCID 18173273—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-(tert-Butyloxycarbonyl)-7-(pyrazin-2-yl)-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 6917947825.6%

Reaction Steps

To a stirred solution of 7-acetyl-3-(tert-butyloxycarbonyl)-2,3,4,5-tetrahydro-1H-3-benzazepine (12 g, 42 mmol) in dioxan (60 ml) was added selenium dioxide (4.61 g, 42 mmol) in dioxan (60 ml) and water (15 ml). The mixture was heated under reflux for 18 h., cooled and the solid residue filtered. The filtrate was evaporated in vacuo and the residue azeotroped with toluene to give an orange gum which was dissolved in ethanol and added dropwise to a stirred solution of ethylenediamine (3 g, 50 mmol) in ethanol at 0° C. After the addition was complete, KOH (2.6 g, 46 mmol) was added and the reaction heated under reflux for 3 h. The reaction mixture was then allowed to cool and evaporated in vacuo. The residue was partitioned between water and dichloromethane and the combined organic extracts dried and evaporated in vacuo to give a brown gum. Purification by silica gel chromatography (eluant 20% EtOAc:hexane) gave the title compound as a yellow oil (3.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429579B2
Source datasetuspto-grants-2008_09
ORD IDord-84ea043f4c9140a5b6734ec0df09a85a
Source noteuspto-grants-2008_09