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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244232Generated: October 30, 2026

Triethylamine → HCID 136395114, compound

https://huagongshe.com/reaction/1244232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 87183058HCID 87183058—
Reactant4-Ethoxy-3-(5-methyl-4-oxo-7-propyl-1,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl)benzene-1-sulfonyl chlorideHCID 135430159—
SolventDichloromethaneHCID 6344—
ProductHCID 136395114HCID 13639511476.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

410 mg (1.0 mmol) of 4-ethoxy-3-(5-methyl-4-oxo-7-propyl-3,4-dihydro-imidazo[5,1-f][1,2,4]triazin-2-yl)-benzenesulphonyl chloride are dissolved in 10 ml of dichloromethane and cooled to 0° C. 590 mg (2.00 mmol) of 1-(5-methyl-4-furoxanecarbonyl)-piperazine trifluoroacetate and 400 mg of triethylamine are added, and the reaction mixture is stirred at room temperature overnight. The mixture is diluted with dichloromethane, the organic phase is washed with ammonium chloride solution, 1M hydrochloric acid and water and dried over sodium sulphate and the solvent is removed under reduced pressure. Crystallization from ether gives 448 mg (74%) of a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122540B2
Source datasetuspto-grants-2006_10
ORD IDord-7dadf9cc992d4b489a5040f04772b586
Source noteuspto-grants-2006_10