Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442980Generated: October 31, 2026

Methanol → N-(3-chloro-4-fluorophenyl)-5,7-dimethoxyquinazolin-4-amine

https://huagongshe.com/reaction/1442980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-(3-chloro-4-fluorophenyl)-5,7-difluoroquinazolin-4-amineHCID 68676704—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-chloro-4-fluorophenyl)-5,7-dimethoxyquinazolin-4-amineHCID 6867552969%

Reaction Conditions

Temperature75 °C

Reaction Steps

Methanol (6.5 ml) and potassium tert-butoxide (18 g) were added sequentially, each in one portion, to a mixture of N-(3-chloro-4-fluorophenyl)-5,7-difluoroquinazolin-4-amine (13.8 g) in THF (270 ml) at room temperature under a nitrogen atmosphere. The mixture was heated at 75° C. for 18 hours 30 minutes and then cooled to room temperature and concentrated in vacuo to leave a brown solid. The solid was cooled to 0° C. and cold water was added and then the precipitate was filtered and dried to leave N-(3-chloro-4-fluorophenyl)-5,7-dimethoxyquinazolin-4-amine as a light brown solid (10.4 g, 69%); Mass spectrum MH+ 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659279B2
Source datasetuspto-grants-2010_02
ORD IDord-e49ab3aeb59a44fc87b6ea50dee6105d
Source noteuspto-grants-2010_02