Development of a Practical Synthesis of a p38 MAP Kinase Inhibitor

Citations Over TimeTop 23% of 2009 papers

Abstract

A practical synthesis of the phthalazine-based p38 MAP kinase inhibitor [(S)-2] was needed for an ongoing program. Vibrational circular dichroism provided the assignment of the absolute stereochemistry of the target compound. The selected synthetic route for (S)-2 required identification of efficient reaction conditions for the construction of carbon−oxygen, carbon−carbon, and carbon−nitrogen bonds to connect the key building blocks. An efficient two-step method (chlorodehydroxylation, aromatic nucleophilic substitution) for the synthesis of arylether [(S)-10] was developed. PAT (in situ Raman spectroscopy) was utilized to monitor and control the formation of a lithium alkoxide in this reaction. The synthesis of (S)-2 was completed using high-yielding Suzuki- and amide-coupling reactions. The isolation conditions for these steps were optimized to obtain material of very high purity without the need for any complicated workup procedures.

Related Papers

• → Synthesis of pyridine-alkoxide ligands for formation of polynuclear complexes(2017)14 cited
• → Ruthenium carbonyl complexes supported by pyridine-alkoxide ligands: synthesis, structure and catalytic oxidation of secondary alcohols(2019)10 cited
• → The Hydrolysis Rate of Betaine Amide and Ester Chlorides(1952)1 cited
• → ChemInform Abstract: EXCHANGE REACTIONS BY SUBSTITUENTS AT PHOSPHORUS(III) ATOM WITH THE PARTICIPATION OF ACETOXY AND AMIDE GROUPS(1981)
• → ChemInform Abstract: Comparative Catalytic C—H vs. C—Si Activation of Arenes with Pd Complexes Directed by Urea or Amide Groups.(2009)