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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Published in | Journal of chemical research Vol. 37; no. 10; pp. 583 - 585 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
LONDON
Sage
01.10.2013
Sage Publications Ltd |
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 1747-5198 2047-6507 |
DOI: | 10.3184/174751913X13782291519608 |