ChemInform Abstract: C- or O-Alkylation of 5-Ethoxycarbonyl-2-hydroxymethyl Pyridine with Arylmethane Derivatives.
β Scribed by C. BISSANTZ; P. BISEL; G. SCHLEWER
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
C-or O-Alkylation of 5-Ethoxycarbonyl-2-hydroxymethyl Pyridine with Arylmethane Derivatives.
-In connection with a research on neurotransmitter inhibitory active compounds, alkylation of pyridine derivative (I) is investigated. Thus, NaH-mediated reaction with diaryl bromomethanes (II) gives the C-alkylation products (III), whereas the benzylbromides (IV) lead to exclusive O-alkylation under the same conditions. O-Diarylmethylated compounds [cf. (VII)] are easily obtained by acidic etherification of (I) with alcohols of type (VI).
π SIMILAR VOLUMES
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Phase Transfer Catalyzed C-vs O-Alkylation of 3-Methyl-1-phenyl-2-pyrazolin-5-one in the Absence or Presence of Carbon Disulfide. -Title compound (I) is treated with different bromoorganic compounds as alkylating agents. Alkylation of pyrazolone (I) by bromoacetaldehyde diethylacetal fails because