HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441237Generated: October 29, 2026
HCID 22405127, compound → HCID 22405050, compound
https://huagongshe.com/reaction/441237
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22405127 | HCID 22405127 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22405050 | HCID 22405050 | — |
Reaction Steps
A mixture of 1,5-bis(4-nitrobenzoyl)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine (737 mg) and iron powder (738 mg) in a mixture of ethanol (10 ml) and acetic acid (1 ml) was refluxed for 2 hours and the solution was cooled to ambient temperature. The mixture was filtered through a bed of celite and the filtrate was evaporated in vacuo. The residue was dissolved in chloroform and the solution was basified with saturated aqueous sodium bicarbonate solution. The solution was filtered through a bed of celite, and then the filtrate was washed with brine. Drying, filtering and the removal of solvents afforded a crude product. The crude product was chromatographed on silica gel (eluent: 2% methanol in chloroform) to give 1,5-bis(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine as a slightly yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05521170 |
|---|
| Source dataset | uspto-grants-1996_05 |
|---|
| ORD ID | ord-419ace0f02894da0ad9999f527ab278c |
|---|
| Source note | uspto-grants-1996_05 |
|---|