HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442981Generated: November 2, 2026
Pyridinium chloride → 4-[3-Chloro-4-fluoroanilino]-7-methoxyquinazolin-5-ol
https://huagongshe.com/reaction/1442981
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | N-(3-chloro-4-fluorophenyl)-5,7-dimethoxyquinazolin-4-amine | HCID 68675529 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-[3-Chloro-4-fluoroanilino]-7-methoxyquinazolin-5-ol | HCID 136347518 | 68.5% |
Reaction Steps
Pyridine hydrochloride (2.33 g) was added in one portion to a stirred mixture of N-(3-chloro-4-fluorophenyl)-5,7-dimethoxyquinazolin-4-amine (6.4 g) in pyridine (75 ml) at room temperature. The reaction mixture was stirred at 115° C. under a nitrogen atmosphere for 23 hours and then the brown solution was cooled to room temperature and the yellow precipitate was filtered and washed with ice cold water to leave a light yellow solid. The solid was taken up in 7N ammonia in methanol and stirred at room temperature for 10 minutes. The solution was filtered and the filtrate was concentrated in vacuo to leave 4-[(3-chloro-4-fluorophenyl)-amino]-7-methoxyquinazolin-5-ol as a light brown solid (4.2 g, 68%); Mass spectrum MH+ 320.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659279B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-1c18b7f572c64c08a55386afa0ea393d |
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| Source note | uspto-grants-2010_02 |
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