HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430490Generated: October 29, 2026
N-(3-Bromophenyl)-6-nitroquinazolin-4-amine → N4-(3-Bromophenyl)quinazoline-4,6-diamine
https://huagongshe.com/reaction/430490
Participants
| Role | Name | HCID | Charge |
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| 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 |
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| Patent number | US06323209B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-7e23f455b4d24ec0928e889d96c5e68e |
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| Source note | uspto-grants-2001_11 |
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