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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-4-fluoroaniline | HCID 9708 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-Chloro-6-(1-imidazolyl)quinazoline | HCID 21847835 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(3-Chloro-4-fluoroanilino)-6-(1-imidazolyl)quinazoline | HCID 21847818 | 19.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05955464 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-5933c9103f02475195a196f2ec7770e7 |
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| Source note | uspto-grants-1999_09 |
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