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Structure of 885693-48-1
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tert-Butyl 4-(5-aminopyridin-2-yl)piperidine-1-carboxylate features a pyridine nitrogen flanked by an electron-rich amine and a sterically hindered tert-butyl ester, enabling stable coupling in late-stage functionalization. This scaffold integrates readily into medicinal chemistry campaigns requiring basic nitrogen positioning and metabolic resilience.
tert-Butyl 4-(5-aminopyridin-2-yl)piperidine-1-carboxylate serves as a versatile building block for the synthesis of bioactive heterocycles, enabling direct incorporation of a pyridinylpiperidine scaffold. The tert-butyl carbamate group provides excellent bench stability and facilitates mild deprotection under acidic conditions. The primary amine is compatible with standard coupling reactions and functionalization protocols, offering a robust platform for medicinal chemistry campaigns targeting kinase inhibitors and CNS-directed therapeutics.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: