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Structure of 848139-78-6
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6-Amino-4-{[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]amino}-7-ethoxyquinoline-3-carbonitrile features a quinoline core bearing an electron-deficient carbonitrile at C3, an ethoxy group at C7, and a chlorinated pyridylmethoxy-substituted aniline moiety. This scaffold integrates a hydrogen-bond donor (amino) and acceptor (nitrile), enabling targeted interactions in kinase inhibition studies. The compound exhibits bench-stable handling under standard conditions and demonstrates enhanced solubility in polar organic solvents due to the balanced polarity of its functional groups.
6-Amino-4-{[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]amino}-7-ethoxyquinoline-3-carbonitrile serves as a versatile building block for medicinal chemistry campaigns targeting kinase inhibitors and antiviral agents. Its core quinoline scaffold enables robust functionalization, while the pyridin-2-ylmethoxy and amino substituents provide orthogonal reactivity for downstream coupling reactions. The molecule exhibits excellent bench stability and facilitates efficient purification via standard chromatographic methods, making it well-suited for high-throughput synthesis workflows.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: