KR870008911A - Carbocyclic purine nucleosides, methods of preparation and uses thereof - Google Patents

Carbocyclic purine nucleosides, methods of preparation and uses thereof Download PDF

Info

Publication number
KR870008911A
KR870008911A KR870002029A KR870002029A KR870008911A KR 870008911 A KR870008911 A KR 870008911A KR 870002029 A KR870002029 A KR 870002029A KR 870002029 A KR870002029 A KR 870002029A KR 870008911 A KR870008911 A KR 870008911A
Authority
KR
South Korea
Prior art keywords
compound
protected
salt
hydroxyl group
antiviral agent
Prior art date
Application number
KR870002029A
Other languages
Korean (ko)
Inventor
요시오 다니야마
다꾸미 하마나
류지 마루모또
나오끼 야마모또
Original Assignee
우메모또 요시마사
다께다이꾸힝 고오교 가부시끼가이샤
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 우메모또 요시마사, 다께다이꾸힝 고오교 가부시끼가이샤 filed Critical 우메모또 요시마사
Publication of KR870008911A publication Critical patent/KR870008911A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

내용없음No content

Description

카르보사이클릭 퓨린 누클레오시드, 그의 제조방법 및 용도Carbocyclic purine nucleosides, methods of preparation and uses thereof

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (14)

하기 일반식(Ⅰ)의 화합물 및 그의 염.Compounds of the general formula (I) [상기 식중, R은 보호될 수도 있는 히드록실기이고, Y는 보호될 수도 있는 퓨린 염기이다.][Wherein R is a hydroxyl group which may be protected and Y is a purine base which may be protected.] 제1항에 있어서, R이 히드록실기이고, Y가 아테닌-9-일, 하이포크산틴-9-일, 구아닌-9-일, 이소구 아닌-9-일, 크산틴-9-일, 3-데아자아데닌-9-일, 7-데아자아데-9-일, 8-데닌아자아데닌-9-일 또는 2,6-디아미노퓨린-9-일임을 특징으로 하는 화합물 및 그의 염.The compound of claim 1, wherein R is a hydroxyl group, Y is athenine-9-yl, hypoxanthine-9-yl, guanine-9-yl, isoguan-9-yl, xanthine-9-yl, Compounds and salts thereof characterized by 3-deazaadenin-9-yl, 7-deazaade-9-yl, 8-denineazadenin-9-yl or 2,6-diaminopurin-9-yl. 제1항에 있어서, 2',3'-디데옥시아리스 테로마이신임을 특징으로 하는 화합물 및 그의 염.The compound and salt thereof according to claim 1, which is 2 ', 3'-dideoxyaris teromycin. 제1항에 있어서, 9-[(1S,4R)-4-히드록시메틸시클로펜탄-1-일] 구아닌임을 특징으로 하는 화합물 및 그의 염.The compound and salt thereof according to claim 1, which is 9-[(1S, 4R) -4-hydroxymethylcyclopentan-1-yl] guanine. 제1항에 있어서, 9-[(1S,4R)-4-히드록시메틸시클로펜탄-1-일] 하이포크산틴임을 특징으로 하는 화합물 및 그의 염.The compound and salt thereof according to claim 1, which is 9-[(1S, 4R) -4-hydroxymethylcyclopentan-1-yl] hypoxanthine. 제1항에 있어서, R이 모노메톡시트리틸 또는 디메톡시트리틸에 의해 보호된 히드록시기임을 특징으로 하는 화합물 및 그의 염.The compound and salt thereof according to claim 1, wherein R is a hydroxy group protected by monomethoxytrityl or dimethoxytrityl. 제1항에 있어서, Y가 벤조일, 이소부티일 또는 아세틸에 의해 보호된 퓨린 염기임 특징으로 하는 화합물 및 그의 염.2. Compounds and salts thereof according to claim 1, wherein Y is a purine base protected by benzoyl, isobutyl or acetyl. 하기 일반식(Ⅱ)의 화합물을 2' 또는 3'-데옥시화를 위하여 환원 반응시킴을 특징으로 하는 하기 일반식(Ⅰ)의 화합물 또는 그 염의 제조방법.A process for producing a compound of formula (I) or a salt thereof, wherein the compound of formula (II) is subjected to a reduction reaction for 2 'or 3'-deoxylation. [상기 식중, R은 보호될 수도 있는 히드록실기이고, Y는 보호될 수도 있는 퓨린 염기이고, R1및 R2중의 하나는 히드록실기이고 다른 하나는 수소이다.][Wherein R is a hydroxyl group which may be protected, Y is a purine base which may be protected, one of R 1 and R 2 is a hydroxyl group and the other is hydrogen.] 제8항에 있어서, 하기 일반식(Ⅱ)의 화합물의 R1또는 R2의 히드록실기를 티오카르보닐화하고, α, α'-아조비스이소부틸로니트릴의 존재하에 트리틸 주석 히드라이드를 이용하여 환원시키고, 필요에 따라 R 및 Y의 보호기를 제거함을 특징으로 하는 일반식(Ⅰ)의 화합물 및 그 염의 제조방법.The hydroxyl group of R 1 or R 2 of the compound of formula (II) is thiocarbonylated and trityl tin hydride in the presence of α, α'-azobisisobutylonitrile. A method for preparing a compound of formula (I) and a salt thereof, wherein the compound is reduced by using to remove R and Y as necessary. [상기 식중, R, Y, R1및 R2는 상기 8항에서의 정의와 동일하다.][Wherein, R, Y, R 1 and R 2 are the same as defined in 8 above.] 유효량의 하기 일반식(Ⅰ)의 화합물 및 그의 염을 함유함을 특징으로 하는 향비루수 제제.Perfumed powder preparation containing an effective amount of the compound of the general formula (I) and salts thereof. [상기 식중, R은 보호될 수도 있는 히드록실기이고, Y는 보호될 수도 있는 퓨린 염기이다.][Wherein R is a hydroxyl group which may be protected and Y is a purine base which may be protected.] 제10항에 있어서, 화합물이 2',3'-디테옥시아리스테로마이신임을 특징으로 하는 향비루스 제제.11. The antiviral agent according to claim 10, wherein the compound is 2 ', 3'-diteoxyaristeromycin. 제10항에 있어서, 화합물이 9-[(1S,4R)-4-히드록시메틸시클로펜틴-1-일] 구아닌임을 특징으로 하는 향비루스 제제.The antiviral agent according to claim 10, wherein the compound is 9-[(1S, 4R) -4-hydroxymethylcyclopentin-1-yl] guanine. 제10항에 있어서, 화합물이 9-[(1S,4R)-4-히드록시메틸시클로펜틴-1-일] 하이포크산틴임을 특징으로 하는 향비루스 제제.The antiviral agent according to claim 10, wherein the compound is 9-[(1S, 4R) -4-hydroxymethylcyclopentin-1-yl] hypoxanthine. 제10항에 있어서, AIDS 비루스의 성장을 억제함을 특징으로 하는 향비루스 제제.The antiviral agent of claim 10, wherein the antiviral agent is characterized by inhibiting the growth of the AIDS virus. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR870002029A 1986-03-06 1987-03-06 Carbocyclic purine nucleosides, methods of preparation and uses thereof KR870008911A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP49395 1986-03-06
JP4939586 1986-03-06

Publications (1)

Publication Number Publication Date
KR870008911A true KR870008911A (en) 1987-10-22

Family

ID=12829840

Family Applications (1)

Application Number Title Priority Date Filing Date
KR870002029A KR870008911A (en) 1986-03-06 1987-03-06 Carbocyclic purine nucleosides, methods of preparation and uses thereof

Country Status (5)

Country Link
JP (1) JPS6310787A (en)
KR (1) KR870008911A (en)
CS (1) CS264290B2 (en)
DD (1) DD255351A5 (en)
SU (1) SU1561826A3 (en)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007504269A (en) 2003-09-05 2007-03-01 スリーエム イノベイティブ プロパティズ カンパニー Method for treating CD5 + B cell lymphoma
AU2004278014B2 (en) 2003-10-03 2011-04-28 3M Innovative Properties Company Alkoxy substituted imidazoquinolines
US7544697B2 (en) 2003-10-03 2009-06-09 Coley Pharmaceutical Group, Inc. Pyrazolopyridines and analogs thereof
MXPA06005910A (en) 2003-11-25 2006-08-23 3M Innovative Properties Co Substituted imidazo ring systems and methods.
WO2005123080A2 (en) 2004-06-15 2005-12-29 3M Innovative Properties Company Nitrogen-containing heterocyclyl substituted imidazoquinolines and imidazonaphthyridines
WO2006009826A1 (en) 2004-06-18 2006-01-26 3M Innovative Properties Company Aryloxy and arylalkyleneoxy substituted thiazoloquinolines and thiazolonaphthyridines
WO2006038923A2 (en) 2004-06-18 2006-04-13 3M Innovative Properties Company Aryl substituted imidazonaphthyridines
US7915281B2 (en) 2004-06-18 2011-03-29 3M Innovative Properties Company Isoxazole, dihydroisoxazole, and oxadiazole substituted imidazo ring compounds and method
CA2594674C (en) 2004-12-30 2016-05-17 3M Innovative Properties Company Substituted chiral fused [1,2]imidazo[4,5-c] ring compounds
JP5543068B2 (en) 2004-12-30 2014-07-09 スリーエム イノベイティブ プロパティズ カンパニー Chiral fused [1,2] imidazo [4,5-c] cyclic compound
CA2597092A1 (en) 2005-02-04 2006-08-10 Coley Pharmaceutical Group, Inc. Aqueous gel formulations containing immune reponse modifiers
WO2006086634A2 (en) 2005-02-11 2006-08-17 Coley Pharmaceutical Group, Inc. Oxime and hydroxylamine substituted imidazo[4,5-c] ring compounds and methods
AU2006232377A1 (en) 2005-04-01 2006-10-12 Coley Pharmaceutical Group, Inc. Pyrazolopyridine-1,4-diamines and analogs thereof
US7943636B2 (en) 2005-04-01 2011-05-17 3M Innovative Properties Company 1-substituted pyrazolo (3,4-C) ring compounds as modulators of cytokine biosynthesis for the treatment of viral infections and neoplastic diseases
US7906506B2 (en) 2006-07-12 2011-03-15 3M Innovative Properties Company Substituted chiral fused [1,2] imidazo [4,5-c] ring compounds and methods

Also Published As

Publication number Publication date
SU1561826A3 (en) 1990-04-30
DD255351A5 (en) 1988-03-30
CS151787A2 (en) 1988-09-16
CS264290B2 (en) 1989-06-13
JPS6310787A (en) 1988-01-18

Similar Documents

Publication Publication Date Title
KR870008911A (en) Carbocyclic purine nucleosides, methods of preparation and uses thereof
GR880300040T1 (en) Nucleoside derivatives and their use in the synthesis of oligonucleotides
KR880012605A (en) Pyrazolo [3,4-d] pyrimidines, methods for their preparation and pharmaceutical compositions containing them
Gaffney et al. Synthesis of O-6-alkylated deoxyguanosine nucleosides
EP0236935A3 (en) Carboxylic purine nucleosides, their production and use
KR840003253A (en) Process for preparing substituted 9- (1 or 3-monoacyloxy or 1,3-diacyloxy-2-propoxymethyl) purine
JPS62161797A (en) 2'-fluoro-arabinofranosylpurine nucleotide
KR890003761A (en) Therapeutic Acyclic Nucleosides
KR927003616A (en) Antiviral pyrimidine nucleosides
NZ223990A (en) Acylated 2',3'-dideoxynucleosides and pharmaceutical compositions
KR900007863A (en) Incense
ES8802363A1 (en) Nucleoside derivatives
KR880003965A (en) Inosose derivative, preparation method and use thereof
DE3568783D1 (en) New 8-substituted nucleoside and purine derivatives, the process for the preparation thereof and the pharmaceutical compositions containing them
KR900009083A (en) 2 ', 3'-dideoxypurine nucleoside / purine nucleoside phosphorylase inhibitor combination therapy and composition
US4914028A (en) Method of preparing beta-2',2'-difluoronucleosides
KR950032164A (en) Cyclopropane derivatives and preparation method thereof
KR890000486A (en) New way
EP0220381A3 (en) Process for synthesis of aluminum coordination compounds
Milne et al. The synthesis and chemical reactivity of 6‐selenoguanosine and certain related derivatives
KR910000710A (en) Sterilizer Nucleosides
KR890002212A (en) Carbocyclic Purine Nucleosides and Uses thereof
US5817639A (en) Purine 4'-thioarabinonucleosides
KR840007090A (en) Method for preparing 3,5-diarabinoside
KR870007944A (en) Manufacturing method of nucleosides

Legal Events

Date Code Title Description
WITB Written withdrawal of application