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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373770Generated: October 30, 2026

Hydrochloric Acid → 6-bromo-1-ethoxycarbonylmethylquinoxalin-2(1H)-one

https://huagongshe.com/reaction/373770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-1,2-dihydroquinoxalin-2-oneHCID 12686394—
SolventDimethylformamideHCID 6228—
Product6-bromo-1-ethoxycarbonylmethylquinoxalin-2(1H)-oneHCID 1980844980%

Reaction Steps

Under a nitrogen atmosphere 6-bromoquinoxalin-2(1H)-one (2.03 g, 9 mmol) (J.Med.Chem., 24, (1981), 93) was dissolved in 22 ml of dry DMF and sodium hydride (0.44 g, 10.8 mmol (60% mineral oil dispersion)) was added. After stirring for 2 h, ethyl bromoacetate (1.25 ml, 11.3 mmol) was added and the mixture was stirred for 3.5 h. The reaction mixture was poured onto crushed ice and acidified (pH=4.5) by addition of dilute hydrochloric acid. The precipitate was filtered off, washed with water and air dried. The crude product (containing a minor fraction of O-alkylated product) was triturated with ether (100 ml), the precipitate filtered off, washed with ether and dried to afford 1.95 g (80%) of pure 6-bromo-1-ethoxycarbonylmethylquinoxalin-2(1H)-one. 1H-NMR (DMSO-d6):δ1.22 (t, 3H), 4.17 (q, 2H), 5.08 (s, 2H), 7.56 (d, 1H), 7.83 (dd, 1H), 8.09 (dd, 1H), 8.37 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166155
Source datasetuspto-grants-1992_11
ORD IDord-86a4749508af47d596394e0586be9092
Source noteuspto-grants-1992_11