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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384618Generated: November 1, 2026

Potassium Carbonate → 7-((2-Chloro-6-methoxy-4-pyridyl)methoxy)-6-methoxy4-phenoxyquinazoline

https://huagongshe.com/reaction/1384618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-4-(chloromethyl)-6-methoxypyridine hydrochlorideHCID 22625059—
Reactant7-Hydroxy-6-methoxy-4-phenoxyquinazolineHCID 135496137—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product7-((2-Chloro-6-methoxy-4-pyridyl)methoxy)-6-methoxy4-phenoxyquinazolineHCID 2262488583.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 7-hydroxy-6-methoxy-4-phenoxyquinazoline (1.1 g, 4.1 mmol), (prepared as described for the starting material in Example 13), 2-chloro-4-chloromethyl-6-methoxypyridine hydrochloride (0.88 g, 3.9 mmol) and potassium carbonate (2.0 g, 14 mmol) in DMF (20 ml) was heated at 80° C. for 1 hour. The mixture was allowed to cool, diluted with water and the precipitated product collected by filtration, washed with water and dried to give 7-((2chloro-6-methoxy-4-pyridyl)methoxy)-6-methoxy-4-phenoxyquinazoline (1.38 g, 79%). 1H NMR Spectrum: (CDCl3) 3.95(s, 3H); 4.04(s, 3H); 5.20(s, 2H); 6.70(s, 1H); 6.95(s, 1H) 7.18(m, 3H); 7.30(t, 1H); 7.40(t, 2H); 7.58(s, 1H); 8.52(s, 1H) MS-ESI: 424 [MH]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258951B1
Source datasetuspto-grants-2001_07
ORD IDord-fb4ba10cdf7b44b1b55b00473576cabe
Source noteuspto-grants-2001_07