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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384677Generated: October 31, 2026

Dimethylformamide → 4-Chloro-6-methoxy-7-(2-(imidazol-1-yl)ethoxy)quinazoline

https://huagongshe.com/reaction/1384677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant7-(2-(Imidazol-1-yl)ethoxy)-6-methoxy-3,4-dihydroquinazolin-4-oneHCID 135490844—
SolventTolueneHCID 1140—
Product4-Chloro-6-methoxy-7-(2-(imidazol-1-yl)ethoxy)quinazolineHCID 1114126159%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 7-(2-(imidazol-1-yl)ethoxy)-6-methoxy-3,4-dihydroquinazolin-4-one (412 mg, 1.44 mmol), thionyl chloride (5 ml) and DMF (0.2 ml) was heated at reflux for 1hour. The mixture was diluted with toluene and the volatiles were removed by evaporation. The residue was suspended in methylene chloride, cooled to 0° C. and aqueous sodium hydrogen carbonate solution was added. The resulting precipitate was collected by filtration and dried under vacuum to give 4-chloro-7-(2-(imidazol-1-yl)ethoxy)-6-methoxyquinazoline (258 mg, 59%). 1H NMR Spectrum: (DMSOd6) 4.01(s, 3H); 4.47(m, 2H); 4.53(m, 2H); 6.89(s, 1H); 7.27(s, 1H); 7.41(s, 1H); 7.49(s, 1H); 7.70(s, 1H); 8.88(s, 1H) MS-ESI: 327 [MNa]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258951B1
Source datasetuspto-grants-2001_07
ORD IDord-8bb8b6d782fe4eeb9270facfde0febc8
Source noteuspto-grants-2001_07