HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3-Bromophenyl)-6-nitroquinazolin-4-amine → N4-(3-Bromophenyl)quinazoline-4,6-diamine
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 Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A mixture of 34.5 g of N-(3-bromophenyl)-6-nitro4-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 | US06251912B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-31228c8fdf0c4187b0d5c92f407c0386 |
| Source note | uspto-grants-2001_06 |