posted on 2020-10-07, 03:32authored byShruti
A. Biyani, Qingqing Qi, Jingze Wu, Yuta Moriuchi, Elizabeth A. Larocque, Herman O. Sintim, David H. Thompson
Developing
continuous syntheses of lead compounds to support in
vivo studies and preclinical evaluation remains an underdeveloped
area. We report a telescoped continuous flow synthesis of an alkynylnaphthyridine
lead compound for the treatment of FLT3 mutations in acute myeloid
leukemia. Different strategies were used to develop the route, including
Design of Experiments (DoE), high-throughput experimentation (HTE),
and application of desorption electrospray ionization mass spectrometry
(DESI-MS) to optimize and telescope the amidation and Sonogashira
couplings to prepare the target compound, HSN608, a potent FLT3 inhibitor.
Findings from these statistical design and automation studies helped
streamline our workflow to achieve 10-fold and 5-fold reductions in
the catalyst and cocatalyst loadings, respectively, in the synthesis.
The application of high-throughput tools combined with a telescoped
continuous synthesis method enabled an efficient and safe synthesis
of this lead compound using the hazardous coupling reagent HATU while
minimizing byproduct formation.