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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454268Generated: October 27, 2026

Potassium Carbonate → 6-Methoxy-4-(3-methylindol-5-yloxy)-7-(2-morpholinoethoxy)quinazoline

https://huagongshe.com/reaction/454268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
Reactant7-Hydroxy-6-methoxy-4-(3-methylindol-5-yloxy)quinazolineHCID 135763115—
SolventDimethylformamideHCID 6228—
Product6-Methoxy-4-(3-methylindol-5-yloxy)-7-(2-morpholinoethoxy)quinazolineHCID 2203093147.1%

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 for the starting material in Example 271), potassium carbonate (1.031 g, 7.47 mmol) and 4-(2-chloroethyl)morpholine hydrochloride (510 mg, 2.74 mmol) in DMF (25 ml) was stirred at 80° C. for 2 hours and allowed to cool to ambient temperature. The reaction mixture was filtered and the filtrate removed 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 recrystallised from ethanol to give 6-methoxy-4-(3-methylindol-5-yloxy)-7-(2-morpholinoethoxy)quinazoline (510 mg, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-cfe58e68751f4859bf60861e084f1a52
Source noteuspto-grants-2013_07