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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453990Generated: November 1, 2026

Potassium Carbonate → 7-(3-(1,1-Dioxothiomorpholino)propoxy)-6-methoxy-4-(quinolin-7-yloxy)quinazoline

https://huagongshe.com/reaction/453990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant4-Chloro-7-(3-(1,1-dioxothiomorpholino)propoxy)-6-methoxyquinazolineHCID 21936000—
Reactant7-HydroxyquinolineHCID 135426866—
SolventDimethylformamideHCID 6228—
Product7-(3-(1,1-Dioxothiomorpholino)propoxy)-6-methoxy-4-(quinolin-7-yloxy)quinazolineHCID 987037673%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-chloro-7-(3-(1,1-dioxothiomorpholino)propoxy)-6-methoxyquinazoline (220 mg, 0.57 mmol), potassium carbonate (106 mg, 0.77 mmol) and 7-hydroxyquinoline (111 mg, 0.76 mmol) in DMF (7.5 ml) was stirred at 100° C. for 5 hours then allowed to cool to ambient temperature. The reaction mixture was treated with 1M aqueous sodium hydroxide solution (40 ml) and stirred at ambient temperature for a few minutes. The crude solid was collected by filtration washing with water. The resultant solid was dissolved in dichloromethane (2 ml) and was filtered through phase separating paper. The filtrate was evaporated under vacuum to give a solid residue which was triturated with ether, filtered and dried to give 7-(3-(1,1-dioxothiomorpholino)propoxy)-6-methoxy-4-(quinolin-7-yloxy)quinazoline (205 mg, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-7ddb8060bdc544a5b9d8d4bb1b57115a
Source noteuspto-grants-2013_07