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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridinium chlorideHCID 10176127—
ReactantN-(3-chloro-4-fluorophenyl)-5,7-dimethoxyquinazolin-4-amineHCID 68675529—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
Product4-[3-Chloro-4-fluoroanilino]-7-methoxyquinazolin-5-olHCID 13634751868.5%

Reaction Conditions

Temperature115 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659279B2
Source datasetuspto-grants-2010_02
ORD IDord-1c18b7f572c64c08a55386afa0ea393d
Source noteuspto-grants-2010_02