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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099276Generated: October 26, 2026

4-(3-Benzyl-1,2,4-oxadiazol-5-yl)piperidine → N-[((1S,2R)-2-{[4-(3-benzyl-1,2,4-oxadiazol-5-yl)piperidin-1-yl]methyl}-1-phenylcyclopropyl)methyl]-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/2099276

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Benzyl-1,2,4-oxadiazol-5-yl)piperidineHCID 41541757—
ReactantN-{[(1S,2R)-2-formyl-1-phenylcyclopropyl]methyl}-N-methylbenzenesulfonamideHCID 57794728—
ProductN-[((1S,2R)-2-{[4-(3-benzyl-1,2,4-oxadiazol-5-yl)piperidin-1-yl]methyl}-1-phenylcyclopropyl)methyl]-N-methylbenzenesulfonamideHCID 9985186—

Reaction Steps

N-{[(1S,2R)-2-formyl-1-phenylcyclopropyl]methyl}-N-methylbenzenesulfonamide and 4-(3-benzyl-1,2,4-oxadiazol-5-yl)piperidine (incorporating by reference as needed WO 00/39125) were reacted as per Preparation 10 to give the title compound. 1H NMR (300 MHz, DMSO-d6) δ 7.69-7.55 (m, 5H), 7.36-7.18 (m, 10H), 4.08 (s, 2H), 3.91 (d, J=13.2 Hz, 1H), 3.08-2.98 (m, 2H), 2.81 (d, J=13.2 Hz, 1H), 2.84-2.78 (m, 1H), 2.59-2.43 (m, 2H), 2.52 (s, 3H), 2.27-1.97 (m, 4H), 1.80-1.66 (m, 2H), 1.45-1.39 (m, 1H), 1.09-0.99 (m, 1H), 0.80 (m, 1H). ES-LCMS m/z 557.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569579B2
Source datasetuspto-grants-2009_08
ORD IDord-77ce63e5bdf24226a96fe650cbe9b3af
Source noteuspto-grants-2009_08