Preparation of 5-methyl-3H-oxazolo[4,5-b]pyridine-2-thione and its reaction with amines

doi:10.1007/BF00505683

Paper

Preparation of 5-methyl-3H-oxazolo[4,5-b]pyridine-2-thione and its reaction with amines

Published May 1, 1981 · K. Davidkov, D. Simov

Chemistry of Heterocyclic Compounds

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Abstract

Abstract5-Methyl-3H-oxazolo[4,5-b]pyridine-2-thione, which exists in the dipolar form, was obtained by the reaction of 6-methyl-2-amino-3-hydroxypyridine with potassium ethylxanthate. The reaction of the product with amines leads to the corresponding thioureas.

Study Snapshot

5-Methyl-3H-oxazolo[4,5-b]pyridine-2-thione is a dipolar product that can be converted into thioureas by reacting with amines.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Paper

Preparation of 5-methyl-3H-oxazolo[4,5-b]pyridine-2-thione and its reaction with amines

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References

Citations

An easy and fast ultrasonic selective S-alkylation of hetaryl thiols at room temperature.

Ultrasonic selective S-alkylation at room temperature allows for the rapid and efficient synthesis of various 2-alkylthio derivatives of hetaryl thiols with high purity.