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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918072Generated: October 25, 2026

Water → 2-Chloro-5-(6,7-dimethoxyquinazolin-4-yloxy)aniline

https://huagongshe.com/reaction/1918072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant2-ChloroquinazolineHCID 74054—
Reactant3-Amino-4-chlorophenolHCID 5070078—
Product2-Chloro-5-(6,7-dimethoxyquinazolin-4-yloxy)anilineHCID 66876386—

Reaction Steps

A solution of 3-amino-4-chlorophenol (1.00 g, 7.0 mmol) and cesium carbonate (3.38 g, 10.4 mmol) in DMF (20 mL) were heated at 80 C for 1 hr. The chloroquinazoline (1.61 g, 7.2 mmol) was added and the mixture heated for an additional hour. The mixture was poured into water (300 mL) and extracted with EtOAc twice. The combined extracts were washed with brine, dried with magnesium sulfate, filtered and concentrated. The residue was purified using silica gel chromatography eluting with EtOAc/hexane (30-70%), the main peak collected and triturated with DCM to afford 2-chloro-5-(6,7-dimethoxyquinazolin-4-yloxy)aniline. 1H NMR (300 MHz, DMSO d6) δ 3.96 (s, 6H), 5.55 (s, 2H), 6.45 (t, 1H), 6.76 (d, 1H), 7.25 (d, 1H), 7.36 (s, 1H), 7.50 (s, 1H), 8.55 (s, 1H); LC-MS (ESI) m/z 332 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-c8daab87a4af45feb3e9508fdf9db2dd
Source noteuspto-grants-2013_12