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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | tert-butyl 7-acetyl-2,3,4,5-tetrahydro-1H-3-benzazepine-3-carboxylate | HCID 18173273 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(tert-Butyloxycarbonyl)-7-(pyrazin-2-yl)-2,3,4,5-tetrahydro-1H-3-benzazepine | HCID 69179478 | 25.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07429579B2 |
|---|
| Source dataset | uspto-grants-2008_09 |
|---|
| ORD ID | ord-84ea043f4c9140a5b6734ec0df09a85a |
|---|
| Source note | uspto-grants-2008_09 |
|---|