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Simple syntheses of benzothiazol‐2‐ylazoles

Simple syntheses of benzothiazol‐2‐ylazoles Syntheses of the title ring systems are described starting with benzothiazol‐2‐ylacetohydrazide (1). Thus, 1 was reacted with carbon disulfide to afford the 2‐methyl heteroaryl derivative 2, which on reaction with hydrazine hydrate yielded the corresponding triazole compound 3. Also, 1 can undergo a reaction with an isothiocyanate to give the N‐thiocarbonyl adduct 4 that can then be cyclized to produce a 2‐methyl heteroaryl analog 5 or 6. Compounds 8 or 9 could be obtained by the reaction of 1 with an aryl aldehyde followed by malononitrile or via its self‐cyclization, respectively. © 1999 John Wiley & Sons, Inc. Heteroatom Chem 10: 177–182, 1999 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

Simple syntheses of benzothiazol‐2‐ylazoles

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References (5)

Publisher
Wiley
Copyright
Copyright © 1999 John Wiley & Sons, Inc.
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/(SICI)1098-1071(1999)10:3<177::AID-HC1>3.0.CO;2-D
Publisher site
See Article on Publisher Site

Abstract

Syntheses of the title ring systems are described starting with benzothiazol‐2‐ylacetohydrazide (1). Thus, 1 was reacted with carbon disulfide to afford the 2‐methyl heteroaryl derivative 2, which on reaction with hydrazine hydrate yielded the corresponding triazole compound 3. Also, 1 can undergo a reaction with an isothiocyanate to give the N‐thiocarbonyl adduct 4 that can then be cyclized to produce a 2‐methyl heteroaryl analog 5 or 6. Compounds 8 or 9 could be obtained by the reaction of 1 with an aryl aldehyde followed by malononitrile or via its self‐cyclization, respectively. © 1999 John Wiley & Sons, Inc. Heteroatom Chem 10: 177–182, 1999

Journal

Heteroatom ChemistryWiley

Published: Jan 1, 1999

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