HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivaloyl chloride → 5-(5-Tert-butyl-1,2,4-oxadiazol-3-yl)-2-chloropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | 6-Chloro-N-hydroxy-nicotinamidine | HCID 33678499 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(5-Tert-butyl-1,2,4-oxadiazol-3-yl)-2-chloropyridine | HCID 86659957 | 21% |
Reaction Steps
A mixture of 1.5 g (8.74 mmol) of 6-chloro-N′-hydroxypyridine-3-carboximidamide and 1.13 mL (9.18 mmol) of trimethylacetyl chloride in 15 mL of toluene is stirred for 1 hour at room temperature and then refluxed for 4 hours. The medium is filtered. The insoluble material formed is dissolved in 15 mL of AcOH and then heated at 60° C. for 5 hours. After cooling to room temperature, the medium is concentrated under reduced pressure and then purified by chromatography on silica gel, eluting with a cyclohexane/EtOAc mixture (9/1). 0.39 g of 5-(5-tert-butyl-1,2,4-oxadiazol-3-yl)-2-chloropyridine is obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359329B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-4a8e9e75ad194f2fb0e0debe6be07851 |
| Source note | uspto-grants-2016_06 |