HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583089Generated: October 30, 2026
N-(3-Bromophenyl)-6-nitroquinazolin-4-amine → N4-(3-Bromophenyl)quinazoline-4,6-diamine
https://huagongshe.com/reaction/583089
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(3-Bromophenyl)-6-nitroquinazolin-4-amine | HCID 5328041 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N4-(3-Bromophenyl)quinazoline-4,6-diamine | HCID 5328042 | — |
Reaction Steps
A mixture of 34.5 g of N-(3-bromophenyl)-6-nitro-4-quinazolinamine and 16.8 g of iron powder in 150 ml of ethanol and 150 ml of glacial acetic acid was heated in an oil bath at 120° C. for 2 hours. After filtration of the solid, solid sodium carbonate was added to the filtrate giving a solid. This was filtered, and the solid was extracted with methanol. The extracts were treated with charcoal and evaporated to a solid. After washing the solid with ether 27.5 g of N-(3-bromophenyl)-4,6-quinazolindiamine was obtained: mass spectrum (m/e): 315.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05929080 |
|---|
| Source dataset | uspto-grants-1999_07 |
|---|
| ORD ID | ord-87728c84929d4fa39f84aa813ad0e9a6 |
|---|
| Source note | uspto-grants-1999_07 |
|---|