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ω-Dialkylaminoalkyl ethers of phenyl-(5-substituted 1-phenyl-1H-pyrazol-4-yl)methanols with analgesic and anti-inflammatory activity

✍ Scribed by Giulia Menozzi; Luisa Mosti; Paola Fossa; Francesca Mattioli; Marco Ghia


Publisher
Journal of Heterocyclic Chemistry
Year
1997
Tongue
English
Weight
344 KB
Volume
34
Category
Article
ISSN
0022-152X

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✦ Synopsis


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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ChemInform Abstract: ω-Dialkylaminoalkyl
✍ G. MENOZZI; L. MOSTI; P. FOSSA; F. MATTIOLI; M. GHIA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

ω-Dialkylaminoalkyl Ethers of Phenyl-(5-substituted 1-phenyl-1Hpyrazol-4-yl)methanols with Analgesic and Antiinflammatory Activity. -A new series of title amino ethers (VI) (12 examples) is synthesized from alcohols (I) and examined for their biological activities. Some derivatives display good ana

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