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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549681Generated: October 26, 2026

Hydrochloric Acid → 5-Methyl-(1,3)oxazolo(4,5-b)pyridine-2-thiol

https://huagongshe.com/reaction/549681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
Reactant6-Methyl-2-nitropyridin-3-olHCID 84801—
ReactantAmmonium formateHCID 2723923—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product5-Methyl-(1,3)oxazolo(4,5-b)pyridine-2-thiolHCID 12664278—

Reaction Conditions

Temperature70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943622B2
Source datasetuspto-grants-2011_05
ORD IDord-a62667c51cc741e298f940b160451c66
Source noteuspto-grants-2011_05