Journal of Heterocyclic Chemistry · 1997 · 89 citations · 3 references
MedicineMedicinal ChemistryPharmacologyDrug DiscoveryPain MedicineSynthetic Medicinal ChemistryAnalgesiaAnalgesic PharmacologyAnti-inflammatory PharmacologyStructure-activity Relationship AnalysisAnalgesic Anti-inflammatory PharmacologyAnalgesic Drug DevelopmentAnalgesic Natural ProductsGrignard Reagent SynthesisMedicinal Chemistry ApplicationsPain PharmacologyPharmacological Pain Relief
Abstract A series of carbinols 3a‐f was prepared starting from methanols 1a‐f via oxidation with pyridinium chlorochromate to aldehydes 2a‐f , followed by a Grignard reaction of the latter. Reaction of 3a‐f with ω‐chloroalkyldialkylamine hydrochlorides afforded a series of aminoether derivatives 4g‐t . Compounds 4i,m‐p,s showed a good analgesic activity in the acetic acid writhing test in mice. Moreover, compounds 4h,1,s exhibited a moderate anti‐inflammatory activity in the carrageenan‐induced edema assay in rats.
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Giulia Menozzi, P. SCHENONE, Luisa Mosti et al. · Journal of Heterocyclic Chemistry · 1993 · 28 citations