This work describes a practical method for coupling chloropyridazines and aryl/hetero aryl amines to get substituted aryl/hetroarylaminopyridazines. The newly developed condition tolerates a wide range of functional groups, including various heterocycles, electron withdrawing/donating groups, and sensitive functional groups. This approach offers a convenient route to a range of secondary heterocyclic aminopyridazines that were otherwise challenging to synthesize.
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Roshan Y. Nimje
Santhosh Rao
Chiradeep Panja
Synthesis
Bristol-Myers Squibb (Germany)
Bristol-Myers Squibb (Japan)
Bristol-Myers Squibb (Netherlands)
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Nimje et al. (Tue,) studied this question.
www.synapsesocial.com/papers/69d894ce6c1944d70ce05b02 — DOI: https://doi.org/10.1055/a-2849-7091