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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Naphthylalanine | HCID 185915 | — |
| Reactant | 4-(4-Ethoxymethyl-5-phenyl-oxazol-2-yl)-piperidine | HCID 18700423 | — |
| Reactant | 5-(2-Chloroethyl)-2-methoxy-benzenesulfonamide | HCID 18700443 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-{2-[4-(4-Ethoxymethyl-5-phenyl-oxazol-3-yl)-piperidin-1-yl]-ethyl}-2-methoxy-benzenesulfonamide | HCID 18700456 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090825 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-2dface9b081c491eaa426a2f50b929d1 |
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| Source note | uspto-grants-2000_07 |
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