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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288991Generated: November 3, 2026

Diisopropylethylamine → 5-{2-[4-(4-Ethoxymethyl-5-phenyl-oxazol-3-yl)-piperidin-1-yl]-ethyl}-2-methoxy-benzenesulfonamide

https://huagongshe.com/reaction/2288991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-NaphthylalanineHCID 185915—
Reactant4-(4-Ethoxymethyl-5-phenyl-oxazol-2-yl)-piperidineHCID 18700423—
Reactant5-(2-Chloroethyl)-2-methoxy-benzenesulfonamideHCID 18700443—
Solvent1,4-DioxaneHCID 31275—
Product5-{2-[4-(4-Ethoxymethyl-5-phenyl-oxazol-3-yl)-piperidin-1-yl]-ethyl}-2-methoxy-benzenesulfonamideHCID 18700456—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 4-(4-ethoxymethyl-5-phenyl-oxazol-2-yl)-piperidine (0.150 g), prepared as in Intermediate 4, in dioxane is added 5-(2-chloro-ethyl)-2-methoxy-benzenesulfonamide (0.170 g), prepared as in Intermediate 1, Nal (0.012 g) and DIEA (0.274 ml). After heating at 100° C. for 18 hours, the reaction mixture is partitioned between EtOAc and dilute NaHCO3 solution. The organic phase is washed with saturated brine, dried (NaSO4) and concentrated. The residue is dissolved in 1:1 MeOH-CH2Cl2 and preadsorbed onto silica gel. Purification by flash chromatography on silica gel using a MeOH-EtOAc gradient (2-20%), affords the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090825
Source datasetuspto-grants-2000_07
ORD IDord-2dface9b081c491eaa426a2f50b929d1
Source noteuspto-grants-2000_07