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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759745Generated: November 2, 2026

1-Methylpiperazine → HCID 135456038, compound

https://huagongshe.com/reaction/1759745

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 135552958HCID 135552958—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 135456038HCID 13545603885.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.42 g (0.92 mmol) of 3-(7-cyclopentyl-5-ethyl-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl)-4-ethoxybenzenesulphonyl chloride are dissolved in 15 ml of dichloromethane and cooled to 0° C. After addition of a spatula tip of 4-dimethylaminopyridine, 0.28 g (2.76 mmol) of N-methylpiperazine 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 and dried over sodium sulphate and the solvent is removed under reduced pressure. Crystallization from ether gives 0.395 g (80%) of a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838459B1
Source datasetuspto-grants-2005_01
ORD IDord-7ed127383ce04bc88f1365ffda6f0ac3
Source noteuspto-grants-2005_01