Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182760Generated: November 3, 2026

Ethyl Acetate → Methyl 6-bromo-2,2-dimethyl-3-oxo-1,2,3,4-tetrahydroquinoxaline-5-carboxylate

https://huagongshe.com/reaction/1182760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantStannous ChlorideHCID 24479—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 6-bromo-3-[(2-ethoxycarbonyl)propan-2-yl]amino-2-nitrobenzoateHCID 67210813—
SolventEthanolHCID 702—
ProductMethyl 6-bromo-2,2-dimethyl-3-oxo-1,2,3,4-tetrahydroquinoxaline-5-carboxylateHCID 2478070970%

Reaction Steps

Methyl 6-bromo-3-[(2-ethoxycarbonyl)propan-2-yl]amino-2-nitrobenzoate (Reference Compound No. 1-(5), 105 mg, 0.26 mmol) was dissolved in anhydrous ethanol (4.5 mL), tin (II) chloride (247 mg, 1.30 mmol) was added thereto, and then the reaction mixture was refluxed for 5 hours. After cooling down, ethyl acetate (25 mL) was added to the reaction mixture, the mixture was neutralized with aqueous sodium hydrogen carbonate solution, and then filtered on celite. After the filtrate was partitioned, the water layer was extracted with ethyl acetate (10 mL, twice), the combined organic layer was washed with water (50 mL, twice) and saturated brine (50 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (56.3 mg) as a pale yellow solid. (Yield 70%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664221B2
Source datasetuspto-grants-2014_03
ORD IDord-c6e625755d8d4416abe122c019e2a5cb
Source noteuspto-grants-2014_03