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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422039Generated: October 25, 2026

Methyl iodide → Methyl 2-(3-chlorobenzyl)-3-methyl-4-oxo-3,4-dihydro-quinazoline-7-carboxylate

https://huagongshe.com/reaction/422039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(3-chlorobenzyl)-4-oxo-3,4-dihydroquinazoline-7-carboxylateHCID 136330125—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-(3-chlorobenzyl)-3-methyl-4-oxo-3,4-dihydro-quinazoline-7-carboxylateHCID 6667728680.6%

Reaction Steps

A mixture of 160 mg of methyl 2-(3-chlorobenzyl)-4-oxo-3,4-dihydroquinazoline-7-carboxylate which was synthesized in Production Example 1, 65 mg of potassium carbonate, 20 mL of acetonitrile and 67 mg of methyl iodide was heated for 2 hours under reflux. Further 20 mg of methyl iodide was added, followed by another hour's heating under reflux. The reaction mixture was allowed to cool off, and then concentrated under reduced pressure, 10 mL of water was added thereto, and extracted with 60 mL of ethyl acetate. The organic layer was washed with 10 mL of saturated saline solution, dried over magnesium sulfate, concentrated under reduced pressure, and the residue was purified on silica gel chromatography (hexane:ethyl acetate=2:1) to provide 130 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101624B2
Source datasetuspto-grants-2012_01
ORD IDord-3c2c53727c53429db6320b957d7f0cfd
Source noteuspto-grants-2012_01