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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050677Generated: October 31, 2026

2-Dimethylaminopyridine → HCID 14304997, compound

https://huagongshe.com/reaction/2050677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 12674946HCID 12674946—
ReactantHCID 14295622HCID 14295622—
SolventDichloromethaneHCID 6344—
ProductHCID 14304997HCID 1430499764.8%

Reaction Conditions

Temperature-20 °C

Reaction Steps

3.6 g of the 4-[4-(2-pyridyl)-piperazin-1-yl]butylamine obtained above were added to a reaction mixture cooled to -20° C. which contained, in 100 ml of absolute dichloromethane, a mixed anhydride produced in a manner analogous to Example 1 (a) from 4.0 g flavone-3-carboxylic acid, 3.367 g dimethylaminopyridine and 1.28 ml methanesulfonyl chloride. The reaction mixture was allowed to warm up to room temperature and stirred at room temperature for two hours. Subsequently the reaction mixture was worked up analogously to Example 3, and the resulting title compound was recrystallized from ethylacetate. There were obtained 4.7 g 3-{4-[4-(2-pyridyl)-piperazin-1-yl]-butylaminocarbonyl)-flavone. yl]-butylaminocarbonyl}-flavone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013852
Source datasetuspto-grants-1991_05
ORD IDord-f940563f59034423b539bb7d307fa587
Source noteuspto-grants-1991_05