HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427273Generated: October 30, 2026
Phosphorus oxychloride → ethyl 5-(1-(4-((tert-butoxycarbonyl)amino)-1H-indazol-1-yl)-1-(4-chlorophenyl)propyl)-1,2,4-oxadiazole-3-carboxylate
https://huagongshe.com/reaction/1427273
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | ethyl 2-amino-2-(((2-(4-((tert-butoxycarbonyl)amino)-1H-indazol-1-yl)-2-(4-chlorophenyl)butanoyl)oxy)imino)acetate | HCID 86705053 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | ethyl 5-(1-(4-((tert-butoxycarbonyl)amino)-1H-indazol-1-yl)-1-(4-chlorophenyl)propyl)-1,2,4-oxadiazole-3-carboxylate | HCID 68175868 | — |
Reaction Steps
To a solution of the product from Step B above (0.18 g, 0.33 mmol) in pyridine (9.0 mL) was added phosphorus oxychloride (0.25 g, 1.65 mmol). The mixture was heated at 70° C. for 7 hours, and stirred at 35° C. overnight, then concentrated to dryness under reduced pressure. The residue was dissolved in EtOAc and washed with saturated NaHCO3, water and brine. The organic layer was separated and dried over Na2SO4. The crude product was purified on a silica gel column using a gradient of 0-50% ethyl acetate in hexanes to give the title compound as light brown solid. LC/MS m/z=526.1[M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933113B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-715bcfc4f05a4332916cbbedd23a61d1 |
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| Source note | uspto-grants-2015_01 |
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