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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791679Generated: November 2, 2026

Potassium Carbonate → Methoxy-7-(3-piperidinopropoxy)quinazoline

https://huagongshe.com/reaction/1791679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-6-methoxy-7-(3-(piperidin-1-YL)propoxy)quinazolineHCID 11002191—
ReactantEthyl 7-chloro-5-hydroxyindole-2-carboxylateHCID 22030936—
SolventDimethylacetamideHCID 31374—
ProductAmmoniaHCID 2222%
ProductMethoxy-7-(3-piperidinopropoxy)quinazolineHCID 69089727215.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-chloro-6-methoxy-7-(3-piperidinopropoxy)quinazoline (84 mg, 0.24 mmol), (prepared as described for the starting material in Example 67), potassium carbonate (162 mg, 1.18 mmol) and ethyl 7-chloro-5-hydroxyindole-2-carboxylate (62 mg, 0.26 mmol) in DMA (2.0 ml) was stirred at 100° C. for 2 hours and allowed to cool to ambient temperature. The reaction mixture was filtered and the filtrate evaporated. The residue was purified by silica column chromatography using gradient elution dichloromethane with 2.5%, 5%, 10% methanol, then dichloromethane with 2% ammonia) to give 4-(7-chloro-2-(ethoxycarbonyl)indol-5-yloxy)-6-(methoxy-7-(3-piperidinopropoxy)quinazoline (78 mg, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-5420ffa646cf4180bb04913a9b4e2ddb
Source noteuspto-grants-2006_07