2005
DOI: 10.1002/jhet.5570420706
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Synthesis of 2,2′-(p-phenylene)bisbenzazoles compounds from terephthalohydroxamoyl chloride

Abstract: In this study, synthesis of symmetric compounds of 2,2′‐(p‐phenylene)bisbenzothiazole, 2,2′‐(p‐phenyl‐ene)bisbenzimidazole and 5,5′‐dimethyl‐2,2′‐(p‐phenylene)bisbenzoxazole were benefited from the reaction of terephthalohydroxamoyl chloride with 2‐amino‐4‐methyl phenol, o‐aminothio phenol and o‐phenylenedi‐amin compounds. The structures of these compounds were confirmed by elemental analysis, mass, 1H‐NMR and FT‐IR techniques.

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Cited by 5 publications
(2 citation statements)
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“…For this reason, a new synthetic procedure to 1,2,4‐triazine derivatives is reported using different starting materials. In our previous study, five‐membered heterocyclic compounds were prepared by the heteroaromatic closing reaction .…”
Section: Resultsmentioning
confidence: 99%
“…For this reason, a new synthetic procedure to 1,2,4‐triazine derivatives is reported using different starting materials. In our previous study, five‐membered heterocyclic compounds were prepared by the heteroaromatic closing reaction .…”
Section: Resultsmentioning
confidence: 99%
“…The reaction proceeded smoothly for 3 h at room temperature using the present protocol, and the desired product 2m was obtained in 94% isolated yield, mp 258–260°C (lit. 258°C) [23].…”
Section: Resultsmentioning
confidence: 99%