ES2078267T3 - H-heteroaril-purin-6-aminas, un procedimiento para su preparacion y su uso como medicamentos. - Google Patents

H-heteroaril-purin-6-aminas, un procedimiento para su preparacion y su uso como medicamentos.

Info

Publication number
ES2078267T3
ES2078267T3 ES90110676T ES90110676T ES2078267T3 ES 2078267 T3 ES2078267 T3 ES 2078267T3 ES 90110676 T ES90110676 T ES 90110676T ES 90110676 T ES90110676 T ES 90110676T ES 2078267 T3 ES2078267 T3 ES 2078267T3
Authority
ES
Spain
Prior art keywords
reduced
heteroaril
purin
hydrogen
aminas
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES90110676T
Other languages
English (en)
Inventor
Richard Charles Effland
Joseph Thomas Klein
Larry Davis
Gordon Edward Olson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aventis Pharmaceuticals Inc
Original Assignee
Hoechst Roussel Pharmaceuticals 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 Hoechst Roussel Pharmaceuticals Inc filed Critical Hoechst Roussel Pharmaceuticals Inc
Application granted granted Critical
Publication of ES2078267T3 publication Critical patent/ES2078267T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52—Purines, e.g. adenine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16—Purine radicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32—Nitrogen atom
    • C07D473/34—Nitrogen atom attached in position 6, e.g. adenine

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Neurosurgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pain & Pain Management (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Saccharide Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Television Signal Processing For Recording (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

Abstract

ESTE INVENTO RELATA UNA AMINA-6-PURIN-HETEROARIL-N DE LA FORMULA DONDE R1 ES HIDROGENO, ALQUIL REDUCIDO, Y ARILREDUCIDOALQUIL; R2 Y R3 SON INDEPENDIENTEMENTE HIDROGENO, ALQUIL REDUCIDO O R2 Y R3 VAN JUNTOS SIENDO ARIL; R4 Y R5 SON INDEPENDIENTEMENTE HIDROGENO, ALQUIL REDUCIDO, O R4 Y R5 VAN JUNTOS SIENDO ARIL; R6 ES HIDROGENO, ALQUIL REDUCIDO, ARIL, ARILREDUCIDOALQUIL, DONDE R2,R3,R4 Y R5 SON COMO SE DEFINIO ANTES, Y SUS SALES DE ADICCION DE ACIDO ACEPTABLES FARMACEUTICAMENTE; Y DONDE SON APLICABLES LOS ISOMEROS GEOMETRICO Y OPTICO Y SUS MEZCLAS RACEMICAS. LOS COMPONENTES DE ESTE INVENTO MUESTRAN UTILIDAD COMO AGENTES ANALGESICOS Y ANTICONVULSANTES.
ES90110676T 1989-06-09 1990-06-06 H-heteroaril-purin-6-aminas, un procedimiento para su preparacion y su uso como medicamentos. Expired - Lifetime ES2078267T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/363,837 US5017578A (en) 1989-06-09 1989-06-09 N-heteroaryl-purin-6-amines useful as analgesic and anticonvulsant agents

Publications (1)

Publication Number Publication Date
ES2078267T3 true ES2078267T3 (es) 1995-12-16

Family

ID=23431950

Family Applications (1)

Application Number Title Priority Date Filing Date
ES90110676T Expired - Lifetime ES2078267T3 (es) 1989-06-09 1990-06-06 H-heteroaril-purin-6-aminas, un procedimiento para su preparacion y su uso como medicamentos.

Country Status (21)

Country Link
US (1) US5017578A (es)
EP (1) EP0402752B1 (es)
JP (1) JPH06102663B2 (es)
KR (2) KR100199524B1 (es)
CN (1) CN1029968C (es)
AT (1) ATE127807T1 (es)
AU (1) AU636351B2 (es)
CA (1) CA2018563C (es)
DE (1) DE69022294T2 (es)
DK (1) DK0402752T3 (es)
ES (1) ES2078267T3 (es)
FI (1) FI902850A0 (es)
GR (1) GR3017743T3 (es)
HU (1) HU207320B (es)
IE (1) IE68433B1 (es)
IL (1) IL94665A (es)
MX (1) MX21088A (es)
NO (1) NO902555L (es)
NZ (1) NZ233970A (es)
PT (1) PT94297B (es)
ZA (1) ZA904443B (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5432164A (en) * 1991-10-24 1995-07-11 Novo Nordisk A/S C2,N6 -disubstituted adenosine derivatives
US5319096A (en) * 1992-04-03 1994-06-07 Hoechst-Roussel Pharmaceuticals Inc. (1H-indol-1-yl)-2-(amino) acetamides and related (1H-indol-1-yl)-(aminoalkyl)amides, pharmaceutical composition and use
US5589467A (en) * 1993-09-17 1996-12-31 Novo Nordisk A/S 2,5',N6-trisubstituted adenosine derivatives
JP3355237B2 (ja) * 1993-10-15 2002-12-09 呉羽化学工業株式会社 Ｎ−（置換アミノ）ピロール誘導体、その製造方法及び除草剤
SK146096A3 (en) * 1994-05-10 1997-07-09 Sandoz Ltd Adenosine derivatives, processes for their preparation, their use for the preparation of drugs, their use in therapy and pharmaceutical compositions containing them
US5789416B1 (en) * 1996-08-27 1999-10-05 Cv Therapeutics Inc N6 mono heterocyclic substituted adenosine derivatives
US6576619B2 (en) 1999-05-24 2003-06-10 Cv Therapeutics, Inc. Orally active A1 adenosine receptor agonists
EP1554572B1 (en) 2001-07-25 2009-10-14 Raptor Pharmaceutical Inc. Compositions and methods for modulating blood-brain barrier transport
CA2535620A1 (en) * 2003-08-15 2005-02-24 Irm Llc 6-substituted anilino purines as rtk inhibitors
CN100447143C (zh) * 2003-08-15 2008-12-31 Irm责任有限公司 作为rtk抑制剂的6-取代的苯胺基嘌呤
EP3827747A1 (en) 2005-04-28 2021-06-02 Otsuka Pharmaceutical Co., Ltd. Pharma-informatics system
EP2063905B1 (en) 2006-09-18 2014-07-30 Raptor Pharmaceutical Inc Treatment of liver disorders by administration of receptor-associated protein (rap)-conjugates
NZ616673A (en) 2009-02-20 2014-08-29 To Bbb Holding B V Glutathione-based drug delivery system
ES2942923T3 (es) 2009-05-06 2023-06-07 Laboratory Skin Care Inc Composiciones de administración dérmica que comprenden complejos de agente activo-partículas de fosfato de calcio y métodos de uso de las mismas
US20120077778A1 (en) 2010-09-29 2012-03-29 Andrea Bourdelais Ladder-Frame Polyether Conjugates
CN104744470A (zh) * 2014-10-31 2015-07-01 合肥平光制药有限公司 一种茶碱的合成方法
US10653681B2 (en) 2016-03-16 2020-05-19 Recurium Ip Holdings, Llc Analgesic compounds
CN106632339B (zh) * 2016-12-16 2018-11-27 温州医科大学 一种6-取代-9h-嘌呤类衍生物及其制备方法和应用

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3016378A (en) * 1959-07-01 1962-01-09 Thomae Gmbh Dr K Amino-substituted purine derivatives
US3796700A (en) * 1970-06-30 1974-03-12 Takedo Chem Ind Ltd Adenosine derivatives and the production thereof
JPS4935635B1 (es) * 1970-12-28 1974-09-25
US3936454A (en) * 1973-08-14 1976-02-03 Warner-Lambert Company 5-Amino-4-chloro-6-(substituted amino)-pyrimidines
US3862189A (en) * 1973-08-14 1975-01-21 Warner Lambert Co Aralkyl-substituted purines and pyrimidines as antianginal bronchodilator agents
JPS57171998A (en) * 1981-04-15 1982-10-22 Fujisawa Pharmaceut Co Ltd Adenosine derivative and its salt, preparation thereof and medicinal composition containing the same
US4514405A (en) * 1981-09-17 1985-04-30 Merck Patent Gesellschaft Mit Beschrankter Haftung Use of adenosine derivatives as anticonvulsants
DE3406533A1 (de) * 1984-02-23 1985-08-29 Boehringer Mannheim Gmbh, 6800 Mannheim Verwendung von adenosin-derivaten als antiallergica und arzneimittel, die diese enthalten
EP0180614B1 (en) * 1984-04-18 1990-03-07 Whitby Research Incorporated N-6 substituted adenosine derivatives as cardiac vasodilators
US4657897A (en) * 1984-06-22 1987-04-14 Warner-Lambert Company N6 -substituted adenosines for treating pain
CA1254888A (en) * 1984-10-26 1989-05-30 Bharat Trivedi N.sup.6-bicycloadenosines
US4752610A (en) * 1985-12-04 1988-06-21 Hoechst-Roussel Pharmaceuticals Inc. N-(pyrrol-1-yl)pyridinamines having memory enhancing properties
US4780452A (en) * 1986-09-08 1988-10-25 Burroughs Wellcome Co. F-substituted-3-β-D-ribofuranosyl-3H-imidazo[4,5-b]pyridines and pharmaceutical compositions thereof

Also Published As

Publication number Publication date
PT94297A (pt) 1991-02-08
NZ233970A (en) 1993-02-25
MX21088A (es) 1993-11-01
HU207320B (en) 1993-03-29
CN1047866A (zh) 1990-12-19
JPH0324080A (ja) 1991-02-01
IE68433B1 (en) 1996-06-12
EP0402752A1 (en) 1990-12-19
EP0402752B1 (en) 1995-09-13
NO902555L (no) 1990-12-10
DK0402752T3 (da) 1996-01-15
CN1029968C (zh) 1995-10-11
DE69022294T2 (de) 1996-03-14
ZA904443B (en) 1991-03-27
IE902077L (en) 1990-12-09
IL94665A0 (en) 1991-04-15
JPH06102663B2 (ja) 1994-12-14
FI902850A0 (fi) 1990-06-07
ATE127807T1 (de) 1995-09-15
IL94665A (en) 1994-06-24
AU5691990A (en) 1990-12-13
GR3017743T3 (en) 1996-01-31
NO902555D0 (no) 1990-06-08
US5017578A (en) 1991-05-21
AU636351B2 (en) 1993-04-29
KR910000730A (ko) 1991-01-30
KR100199524B1 (ko) 1999-06-15
HUT54156A (en) 1991-01-28
PT94297B (pt) 1997-01-31
KR100210179B1 (ko) 1999-07-15
HU903768D0 (en) 1990-11-28
CA2018563A1 (en) 1990-12-09
CA2018563C (en) 2000-09-19
DE69022294D1 (de) 1995-10-19

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