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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496008Generated: October 29, 2026

1-Methylpiperazine → HCID 135489408, compound

https://huagongshe.com/reaction/496008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 135552958HCID 135552958—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 135489408HCID 13548940883.4%

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 numberUS06943163B2
Source datasetuspto-grants-2005_09
ORD IDord-fe7fa9fb08a94930b27f3ca0c41b0b97
Source noteuspto-grants-2005_09