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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016360Generated: October 31, 2026

1-Methylpiperazine → HCID 135489408, compound

https://huagongshe.com/reaction/1016360

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 numberUS06476029B1
Source datasetuspto-grants-2002_11
ORD IDord-d5636c420ff1448c8a6a2872b38d8ddd
Source noteuspto-grants-2002_11