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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068965Generated: October 31, 2026

N-(3-Bromophenyl)-6-nitroquinazolin-4-amine → N4-(3-Bromophenyl)quinazoline-4,6-diamine

https://huagongshe.com/reaction/1068965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Bromophenyl)-6-nitroquinazolin-4-amineHCID 5328041—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—

Reaction Conditions

Temperature120 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-31228c8fdf0c4187b0d5c92f407c0386
Source noteuspto-grants-2001_06