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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877080Generated: October 30, 2026

Potassium Carbonate → (5-(4-(4-((3-Fluorobenzyl)oxy)-3-chloroanilino)-6-quinazolinyl)-2-furancarboxaldehyde

https://huagongshe.com/reaction/877080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantFuran-2-boronic acidHCID 2734357—
Reactant[3-Chloro-4-(3-fluorobenzyloxy)phenyl](6-iodoquinazolin-4-yl)amine hydrochlorideHCID 66623345—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(5-(4-(4-((3-Fluorobenzyl)oxy)-3-chloroanilino)-6-quinazolinyl)-2-furancarboxaldehydeHCID 11181296—

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of [3-chloro-4-(3-fluoro-benzyloxy)-phenyl]-(6-iodo-quinazolin-4-yl)-amine hydrochloride salt (5.05 g, 10 mmol), 2-furylboronic acid (1.85 g, 12 mmol) and palladium catalyst (730 mg, 1.0 mmol) in 10 mL of K2CO3(2.0M), 10 mL of EtOH and 40 mL of DME was heated at 75° C. under nitrogen atmosphere for 4 hr. LS-MS showed the reaction completed. Concentrated the mixture under reduced pressure and washed the residue with water (2×50 mL) then with cool ether (100 mL) to get a gray solid (4.5 g), which was used for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987284B2
Source datasetuspto-grants-2015_03
ORD IDord-255313f93ab0470eabb9fc3f6e909dbb
Source noteuspto-grants-2015_03