Home Chemistry Heterocyclic Building Blocks Piperidines 3-(1-Oxoisoindolin-2-Yl)Piperidine-2,6-Dione
Reduction: The carbonyl groups (the ketone and the amide) can be reduced to their respective alcohols and amines using reducing agents like sodium borohydride or lithium aluminum hydride.
Acylation: The piperidine nitrogen can undergo acylation reactions with acyl chlorides or anhydrides to form amide derivatives.
Ring-opening reactions: The piperidine ring can undergo ring-opening reactions under appropriate conditions. For example, it can react with strong acids to open the ring and form an acyclic compound.
Condensation reactions: The molecule may participate in condensation reactions with other compounds containing reactive functional groups like amines or alcohols.
Oxidation: The molecule can undergo oxidation reactions to convert functional groups within it. For example, the ketone group can be oxidized to a carboxylic acid.
Substitution reactions: The aromatic ring in the isoindoline moiety can undergo electrophilic aromatic substitution reactions, depending on the conditions and reagents used.
Cyclization reactions: The compound may undergo cyclization reactions under certain conditions to form fused ring systems or other cyclic products.
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3-(1-Oxo-4-(prop-2-yn-1-ylamino)isoindolin-2-yl)piperidine-2,6-dione
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3-(7-Bromo-1-oxoisoindolin-2-yl)piperidine-2,6-dione
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(2-(2,6-Dioxopiperidin-3-yl)-1-oxoisoindolin-4-yl)glycine
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3-(4-Amino-1-oxoisoindolin-2-yl)-1-methylpiperidine-2,6-dione
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3-(4-Bromo-1-oxoisoindolin-2-yl)-1-methylpiperidine-2,6-dione
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3-(7-Bromo-4-fluoro-1-oxoisoindolin-2-yl)piperidine-2,6-dione
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3-(7-Fluoro-1-oxoisoindolin-2-yl)piperidine-2,6-dione
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