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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454267Generated: October 31, 2026

Potassium Carbonate → 6-Methoxy-4-(3-methylindol-5-yloxy)-7-(3-morpholinopropoxy)quinazoline

https://huagongshe.com/reaction/454267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3-Chloropropyl)morpholineHCID 95834—
Reactant7-Hydroxy-6-methoxy-4-(3-methylindol-5-yloxy)quinazolineHCID 135763115—
SolventDimethylformamideHCID 6228—
Product6-Methoxy-4-(3-methylindol-5-yloxy)-7-(3-morpholinopropoxy)quinazolineHCID 2203095151%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 7-hydroxy-6-methoxy-4-(3-methylindol-5-yloxy)quinazoline (800 mg, 2.49 mmol), (prepared as described in Example 271), potassium carbonate (687 mg, 4.98 mmol) and 1-chloro-3-morpholinopropane (448 mg, 2.74 mmol), (prepared as described for the starting material in Example 1), in DMF (20 ml) was stirred at 80° C. for 2 hours and allowed to cool to ambient temperature. The reaction mixture was filtered and the filtrate evaporated in vacuo. The residue was purified by silica column chromatography, gradient elution (dichloromethane, 5% methanol/95% dichloromethane, methanol/dichloromethane/0.880 saturated aqueous ammonia (100/8/1)) and the product was recrystallised from ethanol to give 6-methoxy-4-(3-methylindol-5-yloxy)-7-(3-morpholinopropoxy)quinazoline (570 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-918c255bb9664bdeb3723e8625984193
Source noteuspto-grants-2013_07