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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411870Generated: November 3, 2026

1-(5-Ethyl-3-methylpyridin-2-yl)piperazine → HCID 71252481, compound

https://huagongshe.com/reaction/2411870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Ethyl-3-methylpyridin-2-yl)piperazineHCID 58484578—
ReactantHCID 71252272HCID 71252272—
ProductHCID 71252481HCID 7125248146.3%

Reaction Steps

Using methyl 6-(1,1-dioxo-1λ6-isothiazolidin-2-ylmethyl)nicotinate (107 mg) described in Preparation Example 45 and 1-(5-ethyl-3-methylpyridin-2-yl)piperazine (81 mg) described in Preparation Example 81 and by the reaction and treatment in the same manner as in Example 109, [6-(1,1-dioxo-1λ6-isothiazolidin-2-ylmethyl)pyridin-3-yl][4-(5-ethyl-3-methylpyridin-2-yl)piperazin-1-yl]methanone (81 mg) was obtained. The obtained [6-(1,1-dioxo-1λ6-isothiazolidin-2-ylmethyl)pyridin-3-yl][4-(5-ethyl-3-methylpyridin-2-yl)piperazin-1-yl]methanone (81 mg) was dissolved in ethyl acetate/methanol, 2N hydrogen chloride/ethanol solution was added, and the solvent was evaporated under reduced pressure. The obtained residue was suspension washed with diisopropyl ether to give the title compound (83 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-2b28637e1bda48faa9235b9442ad46c6
Source noteuspto-grants-2014_08