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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618671Generated: October 29, 2026

3-Chloro-4-fluoroaniline → 4-(3-Chloro-4-fluoroanilino)-6-(1-imidazolyl)quinazoline

https://huagongshe.com/reaction/618671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-fluoroanilineHCID 9708—
ReactantAmmonium HydroxideHCID 14923—
Reactant4-Chloro-6-(1-imidazolyl)quinazolineHCID 21847835—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product4-(3-Chloro-4-fluoroanilino)-6-(1-imidazolyl)quinazolineHCID 2184781819.7%

Reaction Steps

A mixture of 4-chloro-6-(1-imidazolyl)quinazoline (3.8 g) and 3-chloro-4-fluoroaniline (2.64 g) in isopropanol (50 ml) was heated to reflux for 3 hours. The solid product so obtained was filtered off, washed with isopropanol and with diethyl ether and dried. The solid so obtained was suspended in water (40 ml) and an aqueous ammonium hydroxide solution (15 ml) was added. The mixture was stirred for 10 minutes. the solid was filtered off, washed with 20% aqueous ammonium hydroxide solution, with water, with acetone and with diethyl ether and dried to give 4-(3-chloro-4-fluoroanilino)-6-(1-imidazolyl)quinazoline (1.10 g); NMR Spectrum: (CD3SOCD3) 7.22 (s, 1H), 7.49 (t, 1H), 7.84 (m, 1H), 7.88 (s, 1H), 7.96 (d, 1H), 8.19 (t, 1H), 8.24 (m, 1H), 8.40 (s, 1H), 8.68 (s, 1H), 8.74 (d, 1H), 9.90 (s, 1H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05955464
Source datasetuspto-grants-1999_09
ORD IDord-5933c9103f02475195a196f2ec7770e7
Source noteuspto-grants-1999_09