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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478605Generated: October 26, 2026

2,4-Dichloro-6,7-dimethoxyquinazoline → 2,4-Dichloro-6,7-dimethoxy-5-nitroquinazoline

https://huagongshe.com/reaction/478605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6,7-dimethoxyquinazolineHCID 520327—
ReactantNitronium tetrafluoroborateHCID 11073463—
SolventAcetonitrileHCID 6342—
Product2,4-Dichloro-6,7-dimethoxy-5-nitroquinazolineHCID 2270704874%

Reaction Steps

To a suspension of 2,4-dichloro-6,7-dimethoxyquinazoline (30.0 g, 0.12 mol) in acetonitrile (550 ml) at 0° C. was added nitronium tetrafluoroborate (25.9 g, 0.19 mol) portionwise over 15 min. The reaction was stirred for 0.75 h and then evaporated under reduced pressure. The resulting solid was suspended in a mixture of saturated aqueous sodium bicarbonate and EtOAc and the solid filtered, dissolved in CH2Cl2, dried over MgSO4 and evaporated to give the subtitle compound as a pale yellow solid (27 g). Further material was obtained by separating the organic layer of the filtrate, washing with H2O (1×), saturated brine (1×), drying over MgSO4 and filtering through a pad of silica. Subsequent evaporation under reduced pressure, trituration with EtOAc and filtration gave the subtitle compound as a pale yellow solid (3.9 g, overall yield 88%). Rf 0.24 (etherthexane 1/1, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642242B2
Source datasetuspto-grants-2003_11
ORD IDord-7b5688d7989c4b7f8f5098956cfe1c72
Source noteuspto-grants-2003_11