HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 5-Bromo-2-(5-methyl-1,3,4-oxadiazol-2-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-Bromo-2-(2H-tetrazol-5-yl)pyridine | HCID 23438683 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 5-Bromo-2-(5-methyl-1,3,4-oxadiazol-2-yl)pyridine | HCID 23438643 | 80% |
Reaction Steps
In 130 ml of acetic anhydride was dissolved 8.6 g of 2-(tetrazol-5-yl)-5-bromopyridine prepared in the Preparation example 6. And then the solution was added with 15 ml of pyridine and stirred for 3 hours for reaction. The reaction mixture was added with ethyl acetate and extracted to separate organic layer. And then the organic layer was washed with water and brine. The organic layer was dehydrated, filtrated and concentrated in vacuo to give 7.3 g of the title compound. Yield 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09163043B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-922b978cd7784d899d3e8bca634c9442 |
| Source note | uspto-grants-2015_10 |