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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346571Generated: October 29, 2026

7-Benzyloxy-4-(4-chloro-2,6-difluoroanilino)-6-methoxyquinazoline → 4-(4-Chloro-2,6-difluoroanilino)-7-hydroxy-6-methoxyquinazoline

https://huagongshe.com/reaction/346571

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-4-(4-chloro-2,6-difluoroanilino)-6-methoxyquinazolineHCID 11059028—
SolventTrifluoroacetic acidHCID 6422—
Product4-(4-Chloro-2,6-difluoroanilino)-7-hydroxy-6-methoxyquinazolineHCID 13549685480%

Reaction Steps

A solution of 7-benzyloxy-4-(4-chloro-2,6-difluoroanilino)-6-methoxyquinazoline (200 mg, 0.47 mmol) in TFA (3 ml) was stirred at 80° C. for 3 hours. After cooling, the volatiles were removed under vacuum and the residue was dissolved in water containing 5% methanol. The pH was adjusted to 8 with sodium hydrogen carbonate and the solid was collected by filtration and washed with water. The solid was solubilised in a mixture of ethyl acetate/methanol/methylene chloride (47/6/47). The volatiles were removed under vacuum to give 4-(4-chloro-2,6-difluoroanilino)-7-hydroxy-6-methoxyquinazoline (126 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173038B1
Source datasetuspto-grants-2007_02
ORD IDord-fc57a6c095c341de9bb7dfd25909af83
Source noteuspto-grants-2007_02