What would be some degradation products of these compounds?

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The discussion centers on the degradation of two specific drug compounds over time, focusing on their chemical stability and potential breakdown products. For compound 1, it is noted that the azole ring's CH3 group and sulfur-attached carbons may undergo autooxidation, resulting in alcohols. Additionally, atmospheric moisture could lower the pH, making the cyano (CN) group susceptible to hydrolysis. Compound 2 is also considered for oxidation and hydrolysis, but the conversation highlights a lack of clarity on other degradation pathways for both compounds. The importance of consulting existing literature and conducting empirical experiments is emphasized to better understand the degradation processes and predict the compounds' stability accurately.
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In terms of drug shelf life, what might those compounds degrade into over time? For compound 1, that the azole rings CH3 group as well as the carbons attached to the sulfur could undergo autooxidation to alcohols. I can also see that atmospheric moisture could lower the pH (due to dissolved CO2) and make the CN group hydrolyzable. For compound 2, I can see some potential for oxidation and hydrolysis too but I can't think of anything other than hydrolysis and oxidation reactions for either of these compounds. What other types of degradation could these drugs undergo?
 
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Have you checked the literature? Using empirical rules to try and predict phenomena is okay; ultimately you need to run experiments (or check to see if someone else has already done the work) to get the answer.
 
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