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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469124Generated: October 27, 2026

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

https://huagongshe.com/reaction/469124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(Pyridin-3-yl)methyl]piperazineHCID 156975—
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-(pyridin-3-ylmethyl)piperazin-1-yl]carbonyl}-1,2,4-oxadiazol-5-yl)methyl]benzenesulfonamideHCID 46175206—

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 (27 mg, 0.07 mmol), 1-(pyridin-3-ylmethyl)piperazine (40 mg, 0.23 mmol) and trimethylaluminium (2 M in toluene, 0.08 mL) in DCE (2 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-2ac1081fe7cc410c8a3a7a705d6ec14a
Source noteuspto-grants-2014_01