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Structure of 781649-86-3
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tert-Butyl 4-((2-aminopyridin-3-yl)amino)piperidine-1-carboxylate features a piperidine scaffold bearing a pyridinamine handle, enabling direct conjugation in late-stage functionalization. The tert-butyl ester offers bench-stable protection, simplifying purification and handling during synthetic workflows. This building block integrates efficiently into kinase inhibitor scaffolds and other bioactive heterocycles.
tert-Butyl 4-((2-aminopyridin-3-yl)amino)piperidine-1-carboxylate serves as a versatile building block for pyridine-containing heterocycles, enabling efficient access to bioactive scaffolds via standard amide coupling, Suzuki-Miyaura, and Buchwald-Hartwig reactions. The protected amine and piperidine core offer excellent functional group tolerance, bench stability, and ease of purification, making it ideal for medicinal chemistry campaigns and API intermediate synthesis.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: