KR890016046A - 2-치환-4-치환-1,3-디옥솔란, 이의 합성 및 이의 용도 - Google Patents

2-치환-4-치환-1,3-디옥솔란, 이의 합성 및 이의 용도 Download PDF

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KR890016046A
KR890016046A KR1019890004725A KR890004725A KR890016046A KR 890016046 A KR890016046 A KR 890016046A KR 1019890004725 A KR1019890004725 A KR 1019890004725A KR 890004725 A KR890004725 A KR 890004725A KR 890016046 A KR890016046 A KR 890016046A
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dioxolane
compound according
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hydroxymethyl
lower alkyl
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벨로우 버나드
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원본미기재
아이 에이 에프 바이오켐 인터내쇼날, 인코오포레이티드
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    • 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
    • C07D487/02Heterocyclic 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 two hetero rings
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    • C07D411/14Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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    • A61P31/14Antivirals for RNA viruses
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    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D411/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
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Abstract

내용 없음

Description

2-치환-4-치환-1,3-디옥솔란, 이의 합성 및 이의 용도
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (13)

  1. 하기식(L)의 1,3-디옥솔란, 이것의 기하학적 및 광학이성체 및 그 이성체의 혼합물.
    상기식에서, R1은 수소, 1-16개의 탄소원자를 함유한 아실기, 벤조일 및 적어도 하나의 할로겐, 저급알킬, 저급알콕시, 니트로 및 트리플루오로메틸기에 의해 치환된 벤조일로 구성되는 그룹으로 부터 선택되며 ; R2는 하기 라디칼로 부터 선택된 헤테로시클릭 라디칼이며,
    R3및 R4는 수소 및 저급알킬로 구성되는 그룹으로 부터 각각 선택되며 ; R5는 저급알킬 및 할로겐으로 구성되는 그룹으로 부터 선택된다.
  2. 제 1 항에 있어서, 2-아세톡시메틸-4-(티미딘-1'-일)-1,3-디옥솔란인 화합물.
  3. 제 1 항에 있어서, 2-히드록시메틸-4-(티미딘-1'-일)-1.3-디옥솔란인 화합물.
  4. 제 1 항에 있어서, 2-벤조일 옥시메틸-4-(시토신-1'-일)-1,3-디옥솔란인 화합물.
  5. 제 1 항에 있어서, 트란스-2-하이드로메틸-4-시토신-1'-일)-1,3-디옥솔란인 화합물.
  6. 제 1 항에 있어서, 2-벤조일옥시메틸-4-(아데노신-9'-일)-1,3-디옥솔란인 화합물.
  7. 제 1 항에 있어서, 2-히드록시메틸-4-(아데노신-9')-1,3-디옥솔란인 화합물.
  8. 제 1 항에 있어서, 2-벤조일옥시메틸-4-(2'-아미노-6'-클로로-(푸린-9'-일))-1,3-디옥솔란인 화합물.
  9. 제 1 항에 있어서, 2-히드록시메틸-4-(2'-아미노-6'-클로로-(푸린-9'-일))-1,3-디옥솔란인 화합물.
  10. 제 1 항에 있어서, 2-히드록시메틸-4-(2'-아미노-푸린-9')-1,3-디옥솔란인 화합물.
  11. 제 1 항에 있어서, 2-히드록시메틸-4-(2',6'-디아미노-푸린-9'-일)-1,3-디옥솔란인 화합물.
  12. 제 1 항에 있어서, 2-히드록시메틸-4-(구아니딘-9'-일)-1,3-디옥솔란인 화합물.
  13. 치료학적 유효양의 하기식(L)의 2-치환-4-1,3-디옥솔란, 이것의 기하학적 및 광학 이성질체 및 이것의 이성체 혼합물을 감염된 숙주에 투여하는 것으로 구성되는 비루스 감염의 치료 방법 .
    상기식에서, R1은 수소, 1-16개의 탄소원자를 함유한 아실기, 벤조일 및 적어도 하나의 할로겐, 저급알킬, 저급알콕시, 니트로 및 트리플루오로메틸 기로 치환된 벤조일로 구성되는 그룹으로 부터 선택되며 , R2는 하기 라디칼로 부터 선택된 헤테로시클릭라디칼이며
    R3및 R4는 수소 및 저급알킬로 구성되는 그룹으로 부터 각각 선택되며 R5는 저급알킬 및 할로겐으로 구성되는 그룹으로 부터 선택된다.
    ※ 참고사항 :최초출원 내용에 의하여 공개하는 것임.
KR1019890004725A 1988-04-11 1989-04-11 2-치환-4-치환-1,3-디옥솔란, 이의 합성 및 이의 용도 KR0137023B1 (ko)

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CA179615 1988-04-11

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JP (1) JP3085675B2 (ko)
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AT (1) ATE129247T1 (ko)
AU (1) AU631786B2 (ko)
CA (1) CA1339609C (ko)
DE (1) DE68924549T2 (ko)
DK (1) DK175372B1 (ko)
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Families Citing this family (65)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5597824A (en) * 1987-11-03 1997-01-28 Abbott Laboratories Analogs of oxetanyl purines and pyrimidines
US6350753B1 (en) 1988-04-11 2002-02-26 Biochem Pharma Inc. 2-Substituted-4-substituted-1,3-dioxolanes and use thereof
US6903224B2 (en) 1988-04-11 2005-06-07 Biochem Pharma Inc. Substituted 1,3-oxathiolanes
US6175008B1 (en) 1988-04-11 2001-01-16 Biochem Pharma Inc. Processes for preparing substituted 1,3-oxathiolanes with antiviral properties
US7119202B1 (en) 1989-02-08 2006-10-10 Glaxo Wellcome Inc. Substituted-1,3-oxathiolanes and substituted-1,3-dioxolanes with antiviral properties
US5047407A (en) * 1989-02-08 1991-09-10 Iaf Biochem International, Inc. 2-substituted-5-substituted-1,3-oxathiolanes with antiviral properties
US5466806A (en) * 1989-02-08 1995-11-14 Biochem Pharma Inc. Processes for preparing substituted 1,3-oxathiolanes with antiviral properties
US5270315A (en) * 1988-04-11 1993-12-14 Biochem Pharma Inc. 4-(purinyl bases)-substituted-1,3-dioxlanes
US5041449A (en) * 1988-04-11 1991-08-20 Iaf Biochem International, Inc. 4-(nucleoside base)-substituted-1,3-dioxolanes useful for treatment of retroviral infections
UA45942A (uk) * 1989-02-08 2002-05-15 Біокем Фарма, Інк. 1,3-оксатіолан, його похідні, спосіб (варіанти) його одержання та фармацевтична композиція
IE904378A1 (en) 1989-12-20 1991-07-03 Abbott Lab Analogs of oxetanyl purines and pyrimidines
US6642245B1 (en) 1990-02-01 2003-11-04 Emory University Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane
US5728575A (en) 1990-02-01 1998-03-17 Emory University Method of resolution of 1,3-oxathiolane nucleoside enantiomers
US5204466A (en) * 1990-02-01 1993-04-20 Emory University Method and compositions for the synthesis of bch-189 and related compounds
US5276151A (en) * 1990-02-01 1994-01-04 Emory University Method of synthesis of 1,3-dioxolane nucleosides
US6703396B1 (en) 1990-02-01 2004-03-09 Emory University Method of resolution and antiviral activity of 1,3-oxathiolane nuclesoside enantiomers
GB9009861D0 (en) * 1990-05-02 1990-06-27 Glaxo Group Ltd Chemical compounds
ATE143016T1 (de) * 1990-11-13 1996-10-15 Iaf Biochem Int Substituierte 1,3-oxathiolane mit antiviralen eigenschaften
US5587480A (en) * 1990-11-13 1996-12-24 Biochem Pharma, Inc. Substituted 1,3-oxathiolanes and substituted 1,3-dithiolanes with antiviral properties
US6228860B1 (en) 1990-11-13 2001-05-08 Biochem Pharma Inc. Substituted 1,3-oxathiolanes with antiviral properties
US6369066B1 (en) 1990-11-13 2002-04-09 Biochem Pharma, Inc. Substituted 1,3-oxathiolanes with antiviral properties
US5925643A (en) * 1990-12-05 1999-07-20 Emory University Enantiomerically pure β-D-dioxolane-nucleosides
US5444063A (en) * 1990-12-05 1995-08-22 Emory University Enantiomerically pure β-D-dioxolane nucleosides with selective anti-Hepatitis B virus activity
US5179104A (en) * 1990-12-05 1993-01-12 University Of Georgia Research Foundation, Inc. Process for the preparation of enantiomerically pure β-D-(-)-dioxolane-nucleosides
US5248776A (en) * 1990-12-05 1993-09-28 University Of Georgia Research Foundation, Inc. Process for enantiomerically pure β-L-1,3-oxathiolane nucleosides
US6812233B1 (en) 1991-03-06 2004-11-02 Emory University Therapeutic nucleosides
GB9104740D0 (en) * 1991-03-06 1991-04-17 Wellcome Found Antiviral nucleoside combination
US5817667A (en) * 1991-04-17 1998-10-06 University Of Georgia Research Foudation Compounds and methods for the treatment of cancer
ZA923640B (en) * 1991-05-21 1993-02-24 Iaf Biochem Int Processes for the diastereoselective synthesis of nucleosides
US6005107A (en) * 1992-12-23 1999-12-21 Biochem Pharma, Inc. Antiviral compounds
US6444656B1 (en) 1992-12-23 2002-09-03 Biochem Pharma, Inc. Antiviral phosphonate nucleotides
GB9226879D0 (en) * 1992-12-23 1993-02-17 Iaf Biochem Int Anti-viral compounds
CA2171550C (en) 1993-09-10 2008-08-26 Raymond F. Schinazi Nucleosides with anti-hepatitis b virus activity
US20020120130A1 (en) 1993-09-10 2002-08-29 Gilles Gosselin 2' or 3' -deoxy and 2', 3' -dideoxy-beta-L-pentofuranonucleo-side compounds, method of preparation and application in therapy, especially as anti- viral agents
US5587362A (en) * 1994-01-28 1996-12-24 Univ. Of Ga Research Foundation L-nucleosides
IL115156A (en) * 1994-09-06 2000-07-16 Univ Georgia Pharmaceutical compositions for the treatment of cancer comprising 1-(2-hydroxymethyl-1,3-dioxolan-4-yl) cytosines
US5703058A (en) * 1995-01-27 1997-12-30 Emory University Compositions containing 5-fluoro-2',3'-didehydro-2',3'-dideoxycytidine or a mono-, di-, or triphosphate thereof and a second antiviral agent
US6391859B1 (en) 1995-01-27 2002-05-21 Emory University [5-Carboxamido or 5-fluoro]-[2′,3′-unsaturated or 3′-modified]-pyrimidine nucleosides
US5808040A (en) * 1995-01-30 1998-09-15 Yale University L-nucleosides incorporated into polymeric structure for stabilization of oligonucleotides
ES2276404T3 (es) 1995-06-07 2007-06-16 Emory University Nucleosidos con actividad antivirus de la hepatitis-b.
US5753789A (en) * 1996-07-26 1998-05-19 Yale University Oligonucleotides containing L-nucleosides
US5792773A (en) * 1996-11-15 1998-08-11 Yale University L-β-dioxolane uridine analog administration for treating Epstein-Barr virus infection
US6022876A (en) * 1996-11-15 2000-02-08 Yale University L-β-dioxolane uridine analogs and methods for treating and preventing Epstein-Barr virus infections
WO1998041522A1 (en) 1997-03-19 1998-09-24 Emory University Synthesis, anti-human immunodeficiency virus and anti-hepatitis b virus activities of 1,3-oxaselenolane nucleosides
EP1754710A3 (en) 1998-02-25 2007-12-19 Emory University 2'-Fluoroncucleosides
EA008609B1 (ru) 1998-02-25 2007-06-29 Эмори Юниверсити 2'-фторнуклеозиды
ES2232169T3 (es) 1998-08-12 2005-05-16 Gilead Sciences, Inc. Procedimiento de fabricacion de nucleosidos de 1,3-oxatiolano.
US6979561B1 (en) 1998-10-09 2005-12-27 Gilead Sciences, Inc. Non-homogeneous systems for the resolution of enantiomeric mixtures
ATE315574T1 (de) 1998-11-05 2006-02-15 Centre Nat Rech Scient Nukleoside mit anti-hepatitis b virus wirkung
ATE254126T1 (de) 1998-12-23 2003-11-15 Shire Biochem Inc Antivirale nukleosidanaloga
CN1297281C (zh) 1999-03-29 2007-01-31 希拉生物化学股份有限公司 治疗白血病的方法
US6653318B1 (en) * 1999-07-21 2003-11-25 Yale University 5-(E)-Bromovinyl uracil analogues and related pyrimidine nucleosides as anti-viral agents and methods of use
DE60011637T2 (de) * 1999-09-24 2004-11-11 Shire Biochem Inc., Laval Dioxolan nukleosidanalogen zur behandlung und vorbeugung von viralen infektionen
WO2001032153A2 (en) * 1999-11-04 2001-05-10 Shire Biochem Inc. Method for the treatment or prevention of flaviviridae viral infection using nucleoside analogues
EP1600451A3 (en) 1999-11-12 2008-09-10 Pharmasset, Inc. Synthesis of 2'-deoxy-l-nucleosides
US6436948B1 (en) 2000-03-03 2002-08-20 University Of Georgia Research Foundation Inc. Method for the treatment of psoriasis and genital warts
HUP0301363A2 (hu) * 2000-10-13 2005-12-28 Shire Biochem Inc. Javított intercelluláris bejuttathatóságú dioxolán analógok
CA2788498C (en) 2001-03-01 2016-02-16 Gilead Sciences, Inc. Polymorphic and other crystalline forms of cis-ftc
DE10335061B4 (de) * 2003-07-31 2005-11-17 Wacker-Chemie Gmbh Verfahren zur Herstellung von OH-geschützten [4-(2,6-damino-9H-purin-9-yl)-1,3-dioxolan-2-yl]methanol-Derivaten
US7785839B2 (en) 2004-02-03 2010-08-31 Emory University Methods to manufacture 1,3-dioxolane nucleosides
AU2006294807B2 (en) 2005-09-26 2013-01-17 Gilead Pharmasset Llc Modified 4'-nucleosides as antiviral agents
US8895531B2 (en) 2006-03-23 2014-11-25 Rfs Pharma Llc 2′-fluoronucleoside phosphonates as antiviral agents
ES2500165T3 (es) 2006-06-29 2014-09-30 Kinex Pharmaceuticals, Llc Composiciones de biarilo y métodos para modular una cascada de quinasas
WO2009051848A1 (en) 2007-10-20 2009-04-23 Kinex Pharmaceuticals, Llc Pharmaceutical compositions for modulating a kinase cascade and methods of use thereof
US9675632B2 (en) 2014-08-26 2017-06-13 Enanta Pharmaceuticals, Inc. Nucleoside and nucleotide derivatives

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL76546A (en) * 1984-10-12 1988-12-30 Warner Lambert Co 9-(heteroarylalkyl)-6-purine(thi)one derivatives,their preparation and pharmaceutical compositions containing them
ATE108794T1 (de) * 1985-05-15 1994-08-15 Wellcome Found Therapeutische nucleoside und deren herstellung.

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EP0337713A3 (en) 1990-11-22
GR3017812T3 (en) 1996-01-31
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OA09470A (en) 1992-11-15
ATE129247T1 (de) 1995-11-15
JPH01316375A (ja) 1989-12-21
JP3085675B2 (ja) 2000-09-11
IE891136L (en) 1989-10-11
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HK5996A (en) 1996-01-19
DE68924549D1 (de) 1995-11-23
IE71225B1 (en) 1997-02-12
ZA892645B (en) 1989-12-27
EP0337713B1 (en) 1995-10-18
DK172089A (da) 1989-10-12
IL89921A0 (en) 1989-12-15
AU3264489A (en) 1989-10-12
CA1339609C (en) 1997-12-30
ES2078234T3 (es) 1995-12-16
EP0337713A2 (en) 1989-10-18
DE68924549T2 (de) 1996-04-04
DK175372B1 (da) 2004-09-13
IL89921A (en) 1993-08-18
KR0137023B1 (ko) 1998-04-25

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