Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068044Generated: October 30, 2026

Potassium Carbonate → 7-(Benzyloxy)-4-((4-fluoro-2-methyl-1H-indol-5-yl)oxy)-6-methoxyquinazoline

https://huagongshe.com/reaction/2068044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-fluoro-2-methyl-1H-indol-5-olHCID 10352036—
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 10661998—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product7-(Benzyloxy)-4-((4-fluoro-2-methyl-1H-indol-5-yl)oxy)-6-methoxyquinazolineHCID 1015120457.5%

Reaction Conditions

Temperature95 °C

Reaction Steps

A suspension of 7-benzyloxy-4-chloro-6-methoxyquinazoline free base (10 g, 33.2 mmol), 4-fluoro-5-hydroxy-2-methylindole (5.9 g, 35.7 mmol), (prepared as described for the starting material in Example 1), and potassium carbonate (9.2 g, 66.6 mmol) in NMP (100 ml) was stirred at 95° C. for 1 hour. After cooling, the mixture was partitioned between ethyl acetate and aqueous sodium hydrogen carbonate. The organic layer was separated, washed with brine and dried over magnesium sulphate and evaporated under vacuum. The residue was triturated under acetonitrile and the suspension was cooled. The precipitate was filtered and dried under vacuum to give 7-benzyloxy-4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxyquinazoline (8.2 g, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293902B2
Source datasetuspto-grants-2012_10
ORD IDord-f5d81843921c4a8db09ddaac8e54c446
Source noteuspto-grants-2012_10