HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599560Generated: October 31, 2026
Ammonium Acetate → HCID 24852454, compound
https://huagongshe.com/reaction/599560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2-{4-chloro-1-{1-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]-(E)-methylidene}butyl}-5-(4-fluorophenyl)[1,3,4]oxadiazole | HCID 67067239 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 24852454 | HCID 24852454 | 43.6% |
Reaction Steps
A solution of 2-{4-chloro-1-{1-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]-(E)-methylidene}butyl}-5-(4-fluorophenyl)-[1,3,4]oxadiazole (85 mg) and ammonium acetate (290 mg) in acetic acid (3 mL) was heated under reflux for 10 hours. The reaction solution was left to cool to room temperature and concentrated under reduced pressure. Methylene chloride and a 1 N sodium hydroxide solution were added to the residue, and the organic layer was separated. The resulting organic layer was washed with brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (carrier: Chromatorex™ NH; elution solvent: heptane:ethyl acetate=1:1→ethyl acetate) to obtain 34 mg of the title compound. The property values of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897632B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-868ed2853eef441b94dbfbd98f074b18 |
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| Source note | uspto-grants-2011_03 |
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