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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411473Generated: November 4, 2026

Water → [4-(2,4-Dimethylphenyl)piperazin-1-yl][4-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-3-methoxyphenyl]methanone

https://huagongshe.com/reaction/2411473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(2,4-Xylyl)piperazineHCID 70544—
Reactant4-(4,6-Dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrateHCID 23149411—
Reactant4-(1,1-Dioxo-1lambda6-isothiazolidin-2-yl)-3-methoxybenzoic acidHCID 71252502—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product[4-(2,4-Dimethylphenyl)piperazin-1-yl][4-(1,1-dioxo-1lambda6-isothiazolidin-2-yl)-3-methoxyphenyl]methanoneHCID 7125266888.6%

Reaction Steps

4-(1,1-Dioxo-1λ6-isothiazolidin-2-yl)-3-methoxybenzoic acid (285 mg) described in Preparation Example 21 and 1-(2,4-dimethylphenyl)piperazine (199 mg) were dissolved in a solution of chloroform (2.1 mL) and methanol (2.1 mL), 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (349 mg) was added, and the mixture was stirred at room temperature. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The obtained residue was purified by column chromatography (chloroform:methanol) to give the title compound (411 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-07ccbff127e741c6b77df4bf7ee76613
Source noteuspto-grants-2014_08