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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469123Generated: October 31, 2026

1-((1-Methyl-4-piperidinyl)methyl)piperazine → 4-Methoxy-N,2,6-trimethyl-N-{[3-({4-[(1-methylpiperidin-4-yl)methyl]piperazin-1-yl}carbonyl)-1,2,4-oxadiazol-5-yl]methyl}benzenesulfonamide

https://huagongshe.com/reaction/469123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((1-Methyl-4-piperidinyl)methyl)piperazineHCID 2736942—
ReactantTrimethylaluminumHCID 16682925—
ReactantEthyl 5-({[(4-methoxy-2,6-dimethylphenyl)sulfonyl](methyl)amino}methyl)-1,2,4-oxadiazole-3-carboxylateHCID 58393139—
Solvent1,2-DichloroethaneHCID 11—
Product4-Methoxy-N,2,6-trimethyl-N-{[3-({4-[(1-methylpiperidin-4-yl)methyl]piperazin-1-yl}carbonyl)-1,2,4-oxadiazol-5-yl]methyl}benzenesulfonamideHCID 46176495—

Reaction Steps

The title compound was prepared according to general procedure AT using ethyl 5-({[(4-methoxy-2,6-dimethylphenyl)sulfonyl](methyl)amino}methyl)-1,2,4-oxadiazole-3-carboxylate (35 mg, 0.09 mmol), 1-[(1-methylpiperidin-4-yl)methyl]piperazine (34 mg, 0.17 mmol) and trimethylaluminium (2 M in toluene, 0.08 mL) in DCE (3 mL). A portion of the crude product was purified using prep method D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623859B2
Source datasetuspto-grants-2014_01
ORD IDord-c752ad9d7c59411ea38131be1fb23846
Source noteuspto-grants-2014_01