HUP0302923A2 - Eljárás indol-karbazol-származékok glikozidálására fázisátvivő katalizátorral - Google Patents

Eljárás indol-karbazol-származékok glikozidálására fázisátvivő katalizátorral

Info

Publication number
HUP0302923A2
HUP0302923A2 HU0302923A HUP0302923A HUP0302923A2 HU P0302923 A2 HUP0302923 A2 HU P0302923A2 HU 0302923 A HU0302923 A HU 0302923A HU P0302923 A HUP0302923 A HU P0302923A HU P0302923 A2 HUP0302923 A2 HU P0302923A2
Authority
HU
Hungary
Prior art keywords
group
alkyl
carbon atom
phase transfer
alkylene
Prior art date
Application number
HU0302923A
Other languages
English (en)
Inventor
Shouichi Hiraga
Daniel E. Petrillo
Kai Rossen
Nobuya Satake
Steven A. Weissman
Original Assignee
Banyu Pharmaceutical Co., Ltd.
Merck & Co., Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Banyu Pharmaceutical Co., Ltd., Merck & Co., Inc. filed Critical Banyu Pharmaceutical Co., Ltd.
Publication of HUP0302923A2 publication Critical patent/HUP0302923A2/hu
Publication of HUP0302923A3 publication Critical patent/HUP0302923A3/hu

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/23Heterocyclic radicals containing two or more heterocyclic rings condensed among themselves or condensed with a common carbocyclic ring system, not provided for in groups C07H19/14 - C07H19/22
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H17/00Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
    • C07H17/02Heterocyclic radicals containing only nitrogen as ring hetero atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biotechnology (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

A találmány új glikozidálási eljárásra vonatkozik, amellyel (I)általános képletű vegyületeket lehet előállítani, ahol a képletben aszubsztituensek főbb jelentése a következő: Q jelentése Q, N-R, S vagyCH2; X1 és X2 jelentése 1) H, 2) halogén, 3) OH, 4) CN, 5) NC, 6) CF3,7) (C=O)NO2, 8) (C=O)-(1-6 szénatomos alkil)-csoport, 9) (C=O)O-(1-6szénatomos alkil)-csoport, 10) OCH2OCH2CH2Si(CH3)3, 11) NO2, 12) 9-fluorenil-metil-karbonil-csoport, 13) NR5R6, 14) O-(1-6 szénatomosalkil)-csoport, 15) 1-6 szénatomos alkilcsoport, 16) (1-6 szénatomosalkilén)-aril-csoport vagy 17) O-(1-6 szénatomos alkilén)=aril-csoport; R és R1 jelentése 1) H, 2) (C=O)-(1-6 szénatomos alkil)-csoport, 3) (C=O)CF3, 4) (C=O)O-(1-6 szénatomos alkil)-csoport, 5) 9-fluorenil-metil-karbonil-csoport, 6) furanózcsoport vagy 7)piranózcsoport, amennyiben R és R1 közül az egyik furanózcsoportotvagy piranózcsoportot jelent; R2 és R3 jelentése egymástól függetlenülOH, vagy R2 és R3 együtt oxocsoportot képez; R4 jelentése 1) H, 2) 1-10 szénatomos alkilcsoport, 3) CHO, 4) (C=O)-(1-10 szénatomos alkil)-csoport, 5) (C=O)O-(1-10 szénatomos alkil)-csoport, 6) 0-10 szénatomosalkilén-aril-csoport vagy 7) 0-10 szénatomos alkilén-NR5R6-csoport. Atalálmány szerint előállított vegyületek rák kezelésére alkalmazhatók. Ó
HU0302923A 2000-10-31 2001-10-26 Process for the phase transfer catalyzed glycosidation of indolocarbazole derivatives HUP0302923A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US24467500P 2000-10-31 2000-10-31
PCT/US2001/047603 WO2002036601A2 (en) 2000-10-31 2001-10-26 Phase transfer catalyzed glycosidation of an indolocarbazole

Publications (2)

Publication Number Publication Date
HUP0302923A2 true HUP0302923A2 (hu) 2003-12-29
HUP0302923A3 HUP0302923A3 (en) 2005-02-28

Family

ID=22923680

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0302923A HUP0302923A3 (en) 2000-10-31 2001-10-26 Process for the phase transfer catalyzed glycosidation of indolocarbazole derivatives

Country Status (21)

Country Link
US (2) US6555677B2 (hu)
EP (1) EP1333826A2 (hu)
JP (1) JP3554560B2 (hu)
KR (1) KR100813086B1 (hu)
CN (1) CN1240380C (hu)
AU (2) AU2894502A (hu)
BG (1) BG107737A (hu)
BR (1) BR0115036A (hu)
CA (1) CA2426815A1 (hu)
CZ (1) CZ20031209A3 (hu)
EA (1) EA005209B1 (hu)
HK (1) HK1064053A1 (hu)
HU (1) HUP0302923A3 (hu)
IL (1) IL155543A0 (hu)
IS (1) IS6791A (hu)
MX (1) MXPA03003871A (hu)
NO (1) NO20031922L (hu)
NZ (1) NZ525398A (hu)
PL (1) PL365574A1 (hu)
WO (1) WO2002036601A2 (hu)
ZA (1) ZA200303198B (hu)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6555677B2 (en) * 2000-10-31 2003-04-29 Merck & Co., Inc. Phase transfer catalyzed glycosidation of an indolocarbazole
US7429572B2 (en) * 2003-05-30 2008-09-30 Pharmasset, Inc. Modified fluorinated nucleoside analogues
JPWO2005026185A1 (ja) * 2003-09-16 2006-11-16 萬有製薬株式会社 抗腫瘍性新規インドロピロロカルバゾール誘導体
WO2005116044A1 (ja) * 2004-05-28 2005-12-08 Banyu Pharmaceutical Co.,Ltd インドロピロロカルバゾール誘導体の製造法
CN101023094B (zh) * 2004-07-21 2011-05-18 法莫赛特股份有限公司 烷基取代的2-脱氧-2-氟代-d-呋喃核糖基嘧啶和嘌呤及其衍生物的制备
SI3109244T1 (sl) * 2004-09-14 2019-06-28 Gilead Pharmasset Llc Priprava 2'fluoro-2'-alkil-substituiranih ali drugih neobvezno substituiranih ribofuranozil pirimidinov in purinov in njihovih derivatov
US7537774B2 (en) * 2005-12-23 2009-05-26 Orion Therapeautics, Llc Therapeutic formulation
US7964580B2 (en) 2007-03-30 2011-06-21 Pharmasset, Inc. Nucleoside phosphoramidate prodrugs
US8173621B2 (en) 2008-06-11 2012-05-08 Gilead Pharmasset Llc Nucleoside cyclicphosphates
EA019341B1 (ru) 2008-12-23 2014-02-28 Джилид Фармассет, Ллс. Фосфорамидаты нуклеозидов
WO2010075554A1 (en) 2008-12-23 2010-07-01 Pharmasset, Inc. Synthesis of purine nucleosides
PA8855701A1 (es) 2008-12-23 2010-07-27 Análogos de nucleósidos
US8618076B2 (en) 2009-05-20 2013-12-31 Gilead Pharmasset Llc Nucleoside phosphoramidates
TWI583692B (zh) 2009-05-20 2017-05-21 基利法瑪席特有限責任公司 核苷磷醯胺
BR112012024884A2 (pt) 2010-03-31 2016-10-18 Gilead Pharmasset Llc síntese estereosseletiva de ativos contendo fósforo
PL3290428T3 (pl) 2010-03-31 2022-02-07 Gilead Pharmasset Llc Tabletka zawierająca krystaliczny (S)-2-(((S)-(((2R,3R,4R,5R)-5-(2,4-diokso-3,4-dihydropirymidyn-1(2H)-ylo)-4-fluoro-3-hydroksy-4-metylotetrahydrofuran-2-ylo)metoksy)(fenoksy)fosforylo)amino)propanian izopropylu
EP2646453A1 (en) 2010-11-30 2013-10-09 Gilead Pharmasset LLC Compounds
US8889159B2 (en) 2011-11-29 2014-11-18 Gilead Pharmasset Llc Compositions and methods for treating hepatitis C virus
PT3650014T (pt) 2013-08-27 2021-12-27 Gilead Pharmasset Llc Formulação combinada de dois compostos antivirais

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4808613A (en) 1986-11-21 1989-02-28 Bristol-Myers Company Rebeccamycin derivative containing pharmaceutical composition
GB8818430D0 (en) * 1988-08-03 1988-09-07 Tate & Lyle Plc Process
US5668271A (en) 1991-11-29 1997-09-16 Banyu Pharmaceutical Co., Ltd. Indolopyrrolocarbazole derivatives
US5591842A (en) 1991-11-29 1997-01-07 Banyu Pharmaceutical Co., Ltd. Indolopyrrolocarbazole derivatives
NZ245203A (en) 1991-11-29 1997-07-27 Banyu Pharma Co Ltd 5h-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6h)-dione derivatives substituted in position-13 by a pentose or hexose group; corresponding indolo-furano(anhydride)intermediates
US5437996A (en) 1992-11-24 1995-08-01 Banyu Pharmaceutical Co., Ltd. Microtetraspora strain for preparation of indolopyrrolocarbazole derivatives
US5589365A (en) 1991-11-29 1996-12-31 Banyu Pharmaceutical Co., Ltd. Process for producing glycosylated indolopyrrolocarbazole derivatives by culturing certain microorganisms
US5468872A (en) 1993-09-16 1995-11-21 Cephalon, Inc. K-252a functional derivatives potentiate neurotrophin-3 for the treatment of neurological disorders
EP0675125A1 (en) 1994-03-18 1995-10-04 Kyowa Hakko Kogyo Co., Ltd. A therapeutic agent for thrombocytopenia and indolocarbazole derivatives
US5922860A (en) * 1994-05-09 1999-07-13 Banyu Pharmaceutical Co., Ltd. Antitumor indolopyrrolocarbazole derivatives
US5804564A (en) 1994-05-09 1998-09-08 Banyu Pharmaceutical Co., Ltd. Antitumor indolopyrrolocarbazole derivatives
FR2750135B1 (fr) * 1996-06-20 1998-08-14 Ceca Sa Acides fluoroalkyl glycosides uroniques et lactones-6(3) correspondantes, preparation et utilisations
EP0971717B1 (en) 1996-08-22 2001-12-19 Bristol-Myers Squibb Company Cytotoxic amino sugar and related sugar derivatives of indolopyrrolocarbazoles
US6555677B2 (en) * 2000-10-31 2003-04-29 Merck & Co., Inc. Phase transfer catalyzed glycosidation of an indolocarbazole

Also Published As

Publication number Publication date
AU2894502A (en) 2002-05-15
NO20031922L (no) 2003-06-27
IL155543A0 (en) 2003-11-23
CZ20031209A3 (cs) 2003-10-15
PL365574A1 (en) 2005-01-10
NO20031922D0 (no) 2003-04-29
EA200300525A1 (ru) 2003-08-28
JP3554560B2 (ja) 2004-08-18
AU2002228945B2 (en) 2006-02-02
KR20030082545A (ko) 2003-10-22
CN1240380C (zh) 2006-02-08
IS6791A (is) 2003-04-16
US20040024196A1 (en) 2004-02-05
KR100813086B1 (ko) 2008-03-17
US20020058803A1 (en) 2002-05-16
HK1064053A1 (en) 2005-01-21
EA005209B1 (ru) 2004-12-30
CA2426815A1 (en) 2002-05-10
MXPA03003871A (es) 2003-07-28
US6555677B2 (en) 2003-04-29
CN1482908A (zh) 2004-03-17
EP1333826A2 (en) 2003-08-13
BG107737A (bg) 2004-01-30
HUP0302923A3 (en) 2005-02-28
WO2002036601A3 (en) 2002-11-28
ZA200303198B (en) 2004-04-23
BR0115036A (pt) 2004-02-25
JP2004513131A (ja) 2004-04-30
WO2002036601A2 (en) 2002-05-10
NZ525398A (en) 2004-12-24

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