HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068691Generated: November 2, 2026
Acetic Anhydride → 5-Bromo-2-(5-methyl-1,2,4-oxadiazol-3-yl)pyridine
https://huagongshe.com/reaction/2068691
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 136397847 | HCID 136397847 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Bromo-2-(5-methyl-1,2,4-oxadiazol-3-yl)pyridine | HCID 23438610 | 45% |
Reaction Steps
To a solution of 5-bromo-N′-hydroxypicolinimidamide II (0.75 g, 3.50 mmol) in acetic acid (50.0 mL) was added acetic anhydride (0.75 mL, 7.0 mmol) and the resulting reaction mixture was heated to 100° C. for 2 h. After the completion of reaction (TLC monitoring), acetic acid was distilled off, added water (25.0 mL) and extracted with EtOAc (2×50 mL). The combined organics was washed with brine, dried (Na2SO4), filtered and concentrated to obtain the desired product (0.27 g, 45%). MS: 240.01 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299065B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-0faa30e588764b6fad944d8e1a0bb74f |
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| Source note | uspto-grants-2012_10 |
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