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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735246Generated: October 31, 2026

Triethylamine → HCID 18917535, compound

https://huagongshe.com/reaction/1735246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,5-Dihydropyrrolo[1,2-a]quinoxalineHCID 11805181—
Reactant6-(5-Fluoro-2-methylbenzoyl)aminopyridine-3-carbonyl chlorideHCID 15508250—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 18917535HCID 1891753544.5%

Reaction Steps

To a chilled (0° C.) solution of 0.341 g of 4,5-dihydropyrrolo [1,2-a]quinoxaline and 1.11 ml of triethylamine in 5 ml of dichloromethane is added 1.17 g of 6-[(5-fluoro-2-methylbenzoyl)amino]pyridine-3-carbonyl chloride. The mixture is stirred under argon at room temperature for 16 hours. The mixture is diluted with 50 ml of dichloromethane and 20 ml of water and the organic layer is separated. The organic layer is washed with 20 ml each of 1M NaHCO3 and brine and dried (Na2SO4). The solution is filtered through a thin pad of hydrous magnesium silicate and the pad washed with dichloromethane. The filtrate is concentrated and the residue purified on silica gel prep-plates with ethyl acetate-hexane (1:1) as solvent to give a solid. The solid is crystallized from ethyl acetate to give 0.38 g of crystals, m.p. 190°-196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536718
Source datasetuspto-grants-1996_07
ORD IDord-ba32600293504844bef2c48077e7e6b9
Source noteuspto-grants-1996_07