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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940801Generated: October 31, 2026

Triethylamine → HCID 18917535, compound

https://huagongshe.com/reaction/1940801

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 numberUS05700796
Source datasetuspto-grants-1997_12
ORD IDord-cef2fa6e15a14c8f9d80e31504a5016b
Source noteuspto-grants-1997_12