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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916400Generated: October 30, 2026

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

https://huagongshe.com/reaction/916400

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 numberUS07268230B2
Source datasetuspto-grants-2007_09
ORD IDord-f4aacafd4aae4805a4cb9b220b63ae49
Source noteuspto-grants-2007_09