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. Author manuscript; available in PMC: 2012 May 15.
Published in final edited form as: Bioorg Med Chem Lett. 2011 Mar 4;21(10):3152–3158. doi: 10.1016/j.bmcl.2011.02.114

Scheme 1.

Scheme 1

Reagents and conditions: (i) aryl-boronic acid, Pd(PPh3)4, Na2CO3, DME, H2O,150 °C (μW), 1 h (typical yields: 40–50%) (ii) POCI3, N,N-dimethylaniline, toluene, reflux, 1 h (iii) R,R′NH, iPr2NEt, DMF, rt -to- 60 °C, 2h (typical yields: 80–95%).

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