HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233585Generated: October 31, 2026
HCID 135961971, compound → HCID 135961967, compound
https://huagongshe.com/reaction/2233585
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 135961971 | HCID 135961971 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 135961967 | HCID 135961967 | 10.5% |
Reaction Steps
To a solution of 100 mg of 3-{2-bromo-4-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-phenyl}-4H-[1,2,4]oxadiazol-5-one in 4 ml of pyridine was added 29 mg of copper cyanide. The resulting mixture was stirred under microwave heating at 21° C. for 10 minutes, then concentrated under reduced pressure. The residue was taken into ethyl acetate, washed with a pH 9 aqueous solution of ammonia, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by preparative thin layer chromatography on silica gel (dichloromethane 95/methanol 5) and precipitated from ethyl acetate/diisopropyl ether/pentane to give 9.5 mg of 5-[4-butyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-2-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzonitrile
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709509B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-ab2b963894a24ce6838395bbc86de923 |
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| Source note | uspto-grants-2010_05 |
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