Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolamines

Facile, iodine-mediated access to N-aryl-2-benzoxazolamines has been achieved in a one-pot manner under mild reaction conditions. Reaction of 2-aminophenols and aryl isothiocyanates afforded N-aryl-2-benzoxazolamines in the presence of molecular iodine and pyridine in tetrahydrofuran at room tempera...

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Main Authors: Haruna Nariki, Takuya Miyamura, Daiki Matsui, Motohiro Sonoda, Shinji Tanimori
Format: Article
Language:English
Published: Georg Thieme Verlag KG 2020-10-01
Series:SynOpen
Subjects:
Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0040-1705982
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spelling doaj-961bfeeb28c74b5ca5c50a5a5597001c2020-11-30T06:40:05ZengGeorg Thieme Verlag KGSynOpen2509-93962020-10-0104049910610.1055/s-0040-1705982Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolaminesHaruna NarikiTakuya MiyamuraDaiki MatsuiMotohiro SonodaShinji TanimoriFacile, iodine-mediated access to N-aryl-2-benzoxazolamines has been achieved in a one-pot manner under mild reaction conditions. Reaction of 2-aminophenols and aryl isothiocyanates afforded N-aryl-2-benzoxazolamines in the presence of molecular iodine and pyridine in tetrahydrofuran at room temperature in moderate to excellent yields.http://www.thieme-connect.de/DOI/DOI?10.1055/s-0040-1705982iodinebenzoxazolamineone-pot synthesiscyclode­sulfurizationtransition-metal-free
collection DOAJ
language English
format Article
sources DOAJ
author Haruna Nariki
Takuya Miyamura
Daiki Matsui
Motohiro Sonoda
Shinji Tanimori
spellingShingle Haruna Nariki
Takuya Miyamura
Daiki Matsui
Motohiro Sonoda
Shinji Tanimori
Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolamines
SynOpen
iodine
benzoxazolamine
one-pot synthesis
cyclode­sulfurization
transition-metal-free
author_facet Haruna Nariki
Takuya Miyamura
Daiki Matsui
Motohiro Sonoda
Shinji Tanimori
author_sort Haruna Nariki
title Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolamines
title_short Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolamines
title_full Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolamines
title_fullStr Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolamines
title_full_unstemmed Iodine-Mediated Facile One-Pot Access to N-Aryl-2-benzoxazolamines
title_sort iodine-mediated facile one-pot access to n-aryl-2-benzoxazolamines
publisher Georg Thieme Verlag KG
series SynOpen
issn 2509-9396
publishDate 2020-10-01
description Facile, iodine-mediated access to N-aryl-2-benzoxazolamines has been achieved in a one-pot manner under mild reaction conditions. Reaction of 2-aminophenols and aryl isothiocyanates afforded N-aryl-2-benzoxazolamines in the presence of molecular iodine and pyridine in tetrahydrofuran at room temperature in moderate to excellent yields.
topic iodine
benzoxazolamine
one-pot synthesis
cyclode­sulfurization
transition-metal-free
url http://www.thieme-connect.de/DOI/DOI?10.1055/s-0040-1705982
work_keys_str_mv AT harunanariki iodinemediatedfacileonepotaccesstonaryl2benzoxazolamines
AT takuyamiyamura iodinemediatedfacileonepotaccesstonaryl2benzoxazolamines
AT daikimatsui iodinemediatedfacileonepotaccesstonaryl2benzoxazolamines
AT motohirosonoda iodinemediatedfacileonepotaccesstonaryl2benzoxazolamines
AT shinjitanimori iodinemediatedfacileonepotaccesstonaryl2benzoxazolamines
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