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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469093Generated: October 27, 2026

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

https://huagongshe.com/reaction/469093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Methyl-4-piperidinyl)piperazineHCID 566324—
ReactantTrimethylaluminumHCID 16682925—
ReactantEthyl 5-({Cyclopropyl[(4-methoxy-2,6-dimethylphenyl)sulfonyl]amino}methyl)-1,3,4-oxadiazole-2-carboxylateHCID 58393194—
Solvent1,2-DichloroethaneHCID 11—
ProductN-Cyclopropyl-4-methoxy-2,6-dimethyl-N-[(5-{[4-(1-methylpiperidin-4-yl)piperazin-1-yl]carbonyl}-1,3,4-oxadiazol-2-yl)methyl]benzenesulfonamideHCID 58393238—

Reaction Steps

The title compound was prepared according to general procedure AT using Ethyl 5-({cyclopropyl[(4-methoxy-2,6-dimethylphenyl)sulfonyl]amino}methyl)-1,3,4-oxadiazole-2-carboxylate (30 mg, 0.07 mmol), 1-(1-methylpiperidin-4-yl)piperazine (26 mg, 0.14 mmol) and trimethylaluminium (2 M in toluene, 0.07 mL) in DCE (5 mL). A portion of the crude product was purified using FCC, eluting with 95:4.5:0.5 DCM:MeOH:NH3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623859B2
Source datasetuspto-grants-2014_01
ORD IDord-a146dada81fa4ecbbb4989b57eadf7ce
Source noteuspto-grants-2014_01