HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70144Erstellt: 23. Oktober 2026
Hydrochloric Acid → 5-Methyl[1,3]oxazolo[4,5-b]pyridine-2(3H)-thione
https://huagongshe.com/de/reaction/70144
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 6-Methyl-2-nitropyridin-3-ol | HCID 84801 | — |
| Edukt | Ammonium formate | HCID 2723923 | — |
| Katalysator | Palladium hydroxide | HCID 9942167 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-Methyl[1,3]oxazolo[4,5-b]pyridine-2(3H)-thione | HCID 12664278 | — |
Reaktionsschritte
Ammonium formate (1.64 g, 26 mmol) was added to a suspension of Pd(OH)2 on carbon (˜20% Pd, 0.73 g, 1.0 mmol) and 2-nitro-3-hydroxy-6-methylpyridine (2.0 g, 13 mmol) in EtOH (20 mL). The reaction mixture was heated to 70° C. for 1 h at which point the reaction mixture was allowed to cool to rt and was filtered through Celite®. The filtrate was concentrated under reduced pressure, yielding a thick orangish oil. The material was dissolved in EtOH (25 mL) and potassium hydroxide (0.875 g, 15.6 mmol) and carbon disulfide (15 mL) were added. The reaction mixture was heated to reflux overnight. Upon cooling to rt, the reaction mixture was acidified with 1 N HCl, and the resulting solid was collected by filtration. The solid was washed with water (2×) and air dried followed by drying in a 35° C. vacuum oven. LC-MS: RT=5.58 min, [M+H]+=167.0.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822472B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-64982537af614bce91986c2fc8093296 |
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| Quellennotiz | uspto-grants-2014_09 |
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