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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454076Generated: October 29, 2026

Water → 7-(3-Chloropropoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline

https://huagongshe.com/reaction/454076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant7-hydroxy-6-methoxy-4-(2-methyl-1H-indol-5-yloxy)quinazolineHCID 135763108—
SolventDimethylformamideHCID 6228—
Product7-(3-Chloropropoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazolineHCID 2203087870.4%

Reaction Steps

A suspension of 7-hydroxy-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (321 mg, lmmol), (prepared as described in Example 49), 1-bromo-3-chloropropane (120 μl, 1.2 mmol) and potassium carbonate (359 mg, 2.6 mmol) in DMF (5 ml) was stirred at ambient temperature overnight. After addition of water, the precipitate was collected by filtration, washed with water and dried over phosphorus pentoxide at 60° C. to give 7-(3-chloropropoxy)-6-methoxy-4-(2-methylindol-5-yloxy)quinazoline (280 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-788713520bbe4a818a4d36c34d306527
Source noteuspto-grants-2013_07