MD4201C1 - Способ получения карбонитрилпроизводных спиро[циклопропан-оксиндолов] - Google Patents

Способ получения карбонитрилпроизводных спиро[циклопропан-оксиндолов] Download PDF

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Publication number
MD4201C1
MD4201C1 MDA20120030A MD20120030A MD4201C1 MD 4201 C1 MD4201 C1 MD 4201C1 MD A20120030 A MDA20120030 A MD A20120030A MD 20120030 A MD20120030 A MD 20120030A MD 4201 C1 MD4201 C1 MD 4201C1
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MD
Moldova
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dmso
nmr
chh
mhz
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MDA20120030A
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English (en)
Romanian (ro)
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MD4201B1 (en
Inventor
Наталия СУКМАН
Флюр МАКАЕВ
Original Assignee
Институт Химии Академии Наук Молдовы
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Application filed by Институт Химии Академии Наук Молдовы filed Critical Институт Химии Академии Наук Молдовы
Priority to MDA20120030A priority Critical patent/MD4201C1/ru
Publication of MD4201B1 publication Critical patent/MD4201B1/mo
Publication of MD4201C1 publication Critical patent/MD4201C1/ru

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    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

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  • Indole Compounds (AREA)

Abstract

Изобретение относится к синтезу карбонитрилпроизводных спиро[циклопропан-оксиндолов], которые могут служить прекурсорами в синтезе веществ с анти-ВИЧ активностью.Способ включает реакцию циклопропанирования диазоизатинов с акрилонитрилом, используемого как в качестве реагента, так и растворителя при температуре его кипения.Предложенный способ позволяет более быстрое проведение реакции с высокими выходами, без использования катализаторов и инертной атмосферы.
MDA20120030A 2012-03-21 2012-03-21 Способ получения карбонитрилпроизводных спиро[циклопропан-оксиндолов] MD4201C1 (ru)

Priority Applications (1)

Application Number Priority Date Filing Date Title
MDA20120030A MD4201C1 (ru) 2012-03-21 2012-03-21 Способ получения карбонитрилпроизводных спиро[циклопропан-оксиндолов]

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
MDA20120030A MD4201C1 (ru) 2012-03-21 2012-03-21 Способ получения карбонитрилпроизводных спиро[циклопропан-оксиндолов]

Publications (2)

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MD4201B1 MD4201B1 (en) 2013-02-28
MD4201C1 true MD4201C1 (ru) 2013-09-30

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Application Number Title Priority Date Filing Date
MDA20120030A MD4201C1 (ru) 2012-03-21 2012-03-21 Способ получения карбонитрилпроизводных спиро[циклопропан-оксиндолов]

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MD (1) MD4201C1 (ru)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57102863A (en) * 1980-12-16 1982-06-26 Takeda Chem Ind Ltd Spiroindolinone and its preparation
US6046341A (en) * 1995-10-24 2000-04-04 Sanofi-Synthelabo 3-spiro-indolin-2-one derivatives
WO2004037247A1 (en) * 2002-10-21 2004-05-06 Irm Llc Oxindoles with anti-hiv activity
US20050015776A1 (en) * 2003-06-02 2005-01-20 Bimal Mehta Processing convoy workflow scenarios
WO2007008664A1 (en) * 2005-07-13 2007-01-18 Allergan, Inc. 3-spir0cycl0pr0pyl2-0xind0le kinase inhibitors

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57102863A (en) * 1980-12-16 1982-06-26 Takeda Chem Ind Ltd Spiroindolinone and its preparation
US6046341A (en) * 1995-10-24 2000-04-04 Sanofi-Synthelabo 3-spiro-indolin-2-one derivatives
WO2004037247A1 (en) * 2002-10-21 2004-05-06 Irm Llc Oxindoles with anti-hiv activity
US20050015776A1 (en) * 2003-06-02 2005-01-20 Bimal Mehta Processing convoy workflow scenarios
WO2007008664A1 (en) * 2005-07-13 2007-01-18 Allergan, Inc. 3-spir0cycl0pr0pyl2-0xind0le kinase inhibitors

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
Cava M.P., Litle R.L., Napier D.R. J. Amer. Chem. Soc., 1958, 80, 2257-2262 *
Chen S., Ma J., Wang J. Tetrahedron Lett., 2008, 49, 6781-6783 *
Jiang T., Kuhen K. L., Wolff K., Yin H., Bieza K., Caldwell J., Bursulaya B., Tuntland T., Zhang K., Karanewsky D., He Y. Bioorganic & Medicinal Chemistry Letters, 2006, 16, 2109-2112 *
Jiang T., Kuhen K. L., Wolff K., Yin H., Bieza K., Caldwell J., Bursulaya B., Wu T. Y. H., He Y. Bioorganic & Medicinal Chemistry Letters, 2006, 16, 2105-2108 *
Kumari G., Nutan I., Modi M., Gupta S. K., Singh R. K. Eur. J. Med. Chem., 2011, 46, 1181-1188 *
Marti C., Carreira E.M. J. Am. Chem. Soc., 2005, 127, 11505-11515 *

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