| Literature DB >> 32773890 |
Guanguan Li1, Lalit K Golani1, Rajwana Jahan1, Farjana Rashid1, James M Cook1.
Abstract
An improved synthesis of the anxiolytic, anticonvulsant and antinociceptive compounds: Hz-166, and its bioisosteres 1,2,4-oxadiazole (MP-III-080) and 1,3-oxazole (KRM-II-81) were executed in higher yields and with more facile purification methods (crystallization, etc.) in multigram quantities without column chromatography. In the synthesis of KRM-II-81, an alternative procedure was employed using the selective reducing reagent, potassium diisobutyl-t-butoxy aluminum hydride (PDBBA), to prepare the desired C(3)-aldehyde in the absence of [N(5)-C(6)] imine reduction in good yield on 20 gram scale.Entities:
Keywords: GABAAR; anxiety; benzodiazepines; epilepsy; imine; large scale; neuropathic pain; selective reduction
Year: 2018 PMID: 32773890 PMCID: PMC7413181 DOI: 10.1055/s-0037-1610211
Source DB: PubMed Journal: Synthesis (Stuttg) ISSN: 0039-7881 Impact factor: 3.157