Furo [3, 2-b] indole derivative as well as synthesis method and application thereof

The invention discloses a furo [3, 2-b] indole derivative as well as a synthesis method and application thereof, and the synthesis method comprises the following specific steps: taking a 2-(2-furyl) arylamine compound protected by tosyl as a raw material, adding an organic solvent, a catalyst, an ox...

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Hauptverfasser: LI FEIYUE, WANG CHENGYU, KONG LINGKAI, HAN YU, GUAN PENGCHENG, JIANG YAKUN, MA RONG, LIU MINGHUI, ZHANG TINGHUI, ZHU QIMENG
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creator LI FEIYUE
WANG CHENGYU
KONG LINGKAI
HAN YU
GUAN PENGCHENG
JIANG YAKUN
MA RONG
LIU MINGHUI
ZHANG TINGHUI
ZHU QIMENG
description The invention discloses a furo [3, 2-b] indole derivative as well as a synthesis method and application thereof, and the synthesis method comprises the following specific steps: taking a 2-(2-furyl) arylamine compound protected by tosyl as a raw material, adding an organic solvent, a catalyst, an oxidizing agent and alkali in a protective atmosphere, and performing catalytic synthesis to obtain the furo [3, 2-b] indole derivative as shown in a formula (I). 2-b] indole derivatives. According to the preparation method disclosed by the invention, coupling cyclization of NH and hydrogen at the position 3 of a furan ring is realized under the catalysis of transition metal, and a target product is obtained. Raw materials are simple and easy to obtain; reaction conditions are mild. The invention further discloses application of the furo [3, 2-b] indole derivative shown in the formula (I) in preparation of anti-allergic, anti-tumor, analgesic and anti-inflammatory drugs. 本发明公开了一种呋喃并[3,2-b]吲哚衍生物及其合成方法和应用,该合成方法的具体步骤为:以
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According to the preparation method disclosed by the invention, coupling cyclization of NH and hydrogen at the position 3 of a furan ring is realized under the catalysis of transition metal, and a target product is obtained. Raw materials are simple and easy to obtain; reaction conditions are mild. The invention further discloses application of the furo [3, 2-b] indole derivative shown in the formula (I) in preparation of anti-allergic, anti-tumor, analgesic and anti-inflammatory drugs. 本发明公开了一种呋喃并[3,2-b]吲哚衍生物及其合成方法和应用,该合成方法的具体步骤为:以</description><language>chi ; eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>2022</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20220712&amp;DB=EPODOC&amp;CC=CN&amp;NR=114736212A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20220712&amp;DB=EPODOC&amp;CC=CN&amp;NR=114736212A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>LI FEIYUE</creatorcontrib><creatorcontrib>WANG CHENGYU</creatorcontrib><creatorcontrib>KONG LINGKAI</creatorcontrib><creatorcontrib>HAN YU</creatorcontrib><creatorcontrib>GUAN PENGCHENG</creatorcontrib><creatorcontrib>JIANG YAKUN</creatorcontrib><creatorcontrib>MA RONG</creatorcontrib><creatorcontrib>LIU MINGHUI</creatorcontrib><creatorcontrib>ZHANG TINGHUI</creatorcontrib><creatorcontrib>ZHU QIMENG</creatorcontrib><title>Furo [3, 2-b] indole derivative as well as synthesis method and application thereof</title><description>The invention discloses a furo [3, 2-b] indole derivative as well as a synthesis method and application thereof, and the synthesis method comprises the following specific steps: taking a 2-(2-furyl) arylamine compound protected by tosyl as a raw material, adding an organic solvent, a catalyst, an oxidizing agent and alkali in a protective atmosphere, and performing catalytic synthesis to obtain the furo [3, 2-b] indole derivative as shown in a formula (I). 2-b] indole derivatives. 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subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title Furo [3, 2-b] indole derivative as well as synthesis method and application thereof
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