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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601662Generated: October 30, 2026

Ethyl orthopropionate → 7-Bromo-2-ethyl-3-methyl-4(3H)-quinazolinone

https://huagongshe.com/reaction/601662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthopropionateHCID 66995—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23158201HCID 23158201—
SolventAcetic AcidHCID 176—
Product7-Bromo-2-ethyl-3-methyl-4(3H)-quinazolinoneHCID 23158215—

Reaction Conditions

Temperature100 °C

Reaction Steps

1.5 ml of triethyl orthopropionate and 30 μL of acetic acid were added to 1 ml solution of N-methyl-2-pyrolidine with 796 mg of N-methyl-2-amino4-bromobenzamide, and the mixture was stirred at 100° C. for 1 hour. Saturated sodium bicarbonate aqueous solution was added to the reaction solution, and extracted with ether. Ether layer was washed with saturated saline solution, and dried with anhydrous magnesium sulfate. After distilling out the solvents under reduced pressure, the residues were separated and purified by silicagel column chromatography (hexane/ethyl acetate=4/1), to obtain 653 mg of the above compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-3811d9dc763d4ad09721fce0128ad35d
Source noteuspto-grants-2011_03