HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241698Generated: October 27, 2026
Acetic Acid → 2-Chloro-6-methyl-4-(5-methyl-[1,2,4]oxadiazol-3-yl)-pyridine
https://huagongshe.com/reaction/241698
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 178426669 | HCID 178426669 | — |
| Solvent | Trimethylorthoacetate | HCID 21927715 | — |
| Product | 2-Chloro-6-methyl-4-(5-methyl-[1,2,4]oxadiazol-3-yl)-pyridine | HCID 59534443 | — |
Reaction Steps
2-Chloro-N-hydroxy-6-methyl-isonicotinamidine (120 mg) was suspended in trimethylorthoacetate (3 ml) under inert atmosphere and acetic acid (0.3 ml) was added. The mixture was heated to 100° C. and stirred for 2 h. After cooling to room temperature the solvent was evaporated under reduced pressure and the residue partitioned between EtOAc and aqueous solution of NaHCO3. The organic layer was separated, washed with water and brine, dried under Na2SO4, filtered and the solvent was evaporated under reduced pressure. The crude was purified by flash column chromatography (10 g Isolute® silica gel cartridge; gradient elution: hexane/EtOAc from 10/0 to 9/1) affording the title compound (107 mg). HPLC (Rt)=3.17 min (method L).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653075B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-d7595250bda444e48bb2024365141c22 |
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| Source note | uspto-grants-2014_02 |
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