Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699726Generated: November 1, 2026

Dichloromethane → HCID 178470155, compound

https://huagongshe.com/reaction/1699726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantHCID 18008883HCID 18008883—
ReactantHCID 178418488HCID 178418488—
SolventAcetonitrileHCID 6342—
ProductHCID 178470155HCID 17847015543%

Reaction Steps

To a solution of ethyl 3-ethoxy-7-fluoro-6-nitroquinoxaline-2-carboxylate (6.90 g, 22.3 mmol) in acetonitrile (70 ml) were added dropwise 4-(hydroxymethyl)imidazole hydrochloride (15.1 g, 112 mmol) and successively triethylamine (23.4 ml, 168 mmol) under shading, and the mixture was refluxed for 16 hours. After cooling, methylene chloride was added to the reaction mixture, which was washed with water. The aqueous layer was extracted with methylene chloride, which was combined with foregoing organic layer. After dried over anhydrous sodium sulfate, solvent was distilled off. The residue obtained was purified by means of silica gel column chromatography [ethyl acetate] to obtain 3.69 g of the the title compound as brown power. Yield 43%. Moreover, 2.15 g of ethyl 3-ethoxy-7-fluoro-6-nitroquinoxaline-2-carboxylate were recovered. Yield 31%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06348461B1
Source datasetuspto-grants-2002_02
ORD IDord-50e7b6d85f964696b61d773aa3269899
Source noteuspto-grants-2002_02