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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktCarbon DisulfideHCID 6348—
EduktPotassium HydroxideHCID 14797—
Edukt6-Methyl-2-nitropyridin-3-olHCID 84801—
EduktAmmonium formateHCID 2723923—
KatalysatorPalladium hydroxideHCID 9942167—
LösungsmittelEthanolHCID 702—
Produkt5-Methyl[1,3]oxazolo[4,5-b]pyridine-2(3H)-thioneHCID 12664278—

Reaktionsbedingungen

Temperatur70 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822472B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-64982537af614bce91986c2fc8093296
Quellennotizuspto-grants-2014_09