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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454222Generated: October 30, 2026

4-fluoro-2-methyl-1H-indol-5-ol → 4-(4-Fluoro-2-methylindol-5-yloxy)-6-methoxy-7-(3-piperidinopropoxy)quinazoline

https://huagongshe.com/reaction/454222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-fluoro-2-methyl-1H-indol-5-olHCID 10352036—
Reactant4-Chloro-6-methoxy-7-(3-(piperidin-1-YL)propoxy)quinazolineHCID 11002191—
Product4-(4-Fluoro-2-methylindol-5-yloxy)-6-methoxy-7-(3-piperidinopropoxy)quinazolineHCID 1018329283.6%

Reaction Steps

Using an analogous procedure to that described in Example 237, 4-chloro-6-methoxy-7-(3-piperidinopropoxy)quinazoline (1.65 g, 4.89 mmol), (prepared as described for the starting material in Example 67), was reacted with 4-fluoro-5-hydroxy-2-methylindole (970 mg, 5.88 mmol), (prepared as described for the starting material in Example 237), to give 4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxy-7-(3-piperidinopropoxy)quinazoline (1.9 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-fff1e744a86f48faa67cfaacc45da8b2
Source noteuspto-grants-2013_07