HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71273Generated: October 28, 2026
Tetrahydrofuran → Tert-butyl 3-(4-(5-(2-(1-(3,5-dichlorophenyl)cyclohexyl)ethyl)-1,2,4-oxadiazol-3-yl)phenyl)-3-hydroxyazetidine-1-carboxylate
https://huagongshe.com/reaction/71273
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Bis(2-oxo-3-oxazolidinyl)phosphinic chloride | HCID 152842 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 66686108 | HCID 66686108 | — |
| Reactant | tert-butyl 3-hydroxy-3-(4-(N'-hydroxycarbamimidoyl)phenyl)azetidine-1-carboxylate | HCID 86688207 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 3-(4-(5-(2-(1-(3,5-dichlorophenyl)cyclohexyl)ethyl)-1,2,4-oxadiazol-3-yl)phenyl)-3-hydroxyazetidine-1-carboxylate | HCID 66692429 | 75.2% |
Reaction Steps
BOP-Cl (36.4 mg, 0.143 mmol) was added to a mixture of crude tert-butyl 3-hydroxy-3-(4-(N′-hydroxycarbamimidoyl)phenyl)azetidine-1-carboxylate (Intermediate 4, 40 mg, 0.13 mmol), 3-(1-(3,5-dichlorophenyl)cyclohexyl)propanoic acid (39.2 mg, 0.13 mmol) and diisopropylethyl amine (0.045 mL, 0.26 mmol) in DMF (3 mL). The mixture was stirred at room temperature for 2 h, and a 1M solution of tetra-n-butylammonium fluoride in THF (0.13 mL, 0.13 mmol) was added. The mixture was heated to 80° C. overnight, diluted with ethyl acetate, and washed with saturated aqueous NaCl solution. The organic layer was dried (MgSO4), filtered, and concentrated. The crude product was purified on a 24 g ISCO cartridge and eluted with EtOAc-hexanes gradient to obtain tert-butyl 3-(4-(5-(2-(1-(3,5-dichlorophenyl)cyclohexyl)ethyl)-1,2,4-oxadiazol-3-yl)phenyl)-3-hydroxyazetidine-1-carboxylate (56 mg, 50% yield, HPLC purity: 80%). HPLC retention time=4.71 minutes (Waters Sunfire C18 4.6×50 mm) eluting with 10-90% aqueous methanol with 0.1% TFA over a 4 minute gradient. LC/MS: m/e 572.25 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822510B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-4f4cf390d2904f1ca08bbfc063a9f30b |
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| Source note | uspto-grants-2014_09 |
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