Synthesis and spectroscopic characterisation of novel roflumilast analogues

A series of new N-heterocyclic or phenoxy substituted roflumilast analogues have been designed and synthesised. N-heterocyclic or phenoxy substituted benzaldehydes were first prepared from 3-hydroxy-4-methoxybenzaldehbyde and 1-bromo-3-chloropropane by an alkylation reaction. The roflumilast analogu...

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Bibliographic Details
Published inJournal of chemical research Vol. 37; no. 10; pp. 583 - 585
Main Authors Sun, Gangchun, Si, Yuhui, Song, Ge, Mai, Wenpeng, Li, Zhicheng
Format Journal Article
LanguageEnglish
Published LONDON Sage 01.10.2013
Sage Publications Ltd
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Summary:A series of new N-heterocyclic or phenoxy substituted roflumilast analogues have been designed and synthesised. N-heterocyclic or phenoxy substituted benzaldehydes were first prepared from 3-hydroxy-4-methoxybenzaldehbyde and 1-bromo-3-chloropropane by an alkylation reaction. The roflumilast analogues were then obtained by oxidation, acylation, amidation and alkylation reactions. These compounds were characterised by H-1 NMR, IR, ESI-MS and elemental analyses.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:1747-5198
2047-6507
DOI:10.3184/174751913X13782291519608