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FI80454B - Foerfarande foer framstaellning av farmakologiskt vaerdefulla 2-piperazino-pteridiner. - Google Patents

Foerfarande foer framstaellning av farmakologiskt vaerdefulla 2-piperazino-pteridiner. Download PDF

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Publication number
FI80454B
FI80454B FI842622A FI842622A FI80454B FI 80454 B FI80454 B FI 80454B FI 842622 A FI842622 A FI 842622A FI 842622 A FI842622 A FI 842622A FI 80454 B FI80454 B FI 80454B
Authority
FI
Finland
Prior art keywords
piperazino
pteridine
group
formula
compound
Prior art date
Application number
FI842622A
Other languages
English (en)
Finnish (fi)
Other versions
FI80454C (sv
FI842622A (fi
FI842622A0 (fi
Inventor
Berthold Narr
Erich Mueller
Josef Nickl
Josef Roch
Rainer Zimmermann
Johannes Weisenberger
Walter Haarmann
Original Assignee
Thomae Gmbh Dr K
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 Thomae Gmbh Dr K filed Critical Thomae Gmbh Dr K
Publication of FI842622A0 publication Critical patent/FI842622A0/fi
Publication of FI842622A publication Critical patent/FI842622A/fi
Application granted granted Critical
Publication of FI80454B publication Critical patent/FI80454B/fi
Publication of FI80454C publication Critical patent/FI80454C/sv

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D475/00Heterocyclic compounds containing pteridine ring systems
    • C07D475/06Heterocyclic compounds containing pteridine ring systems with a nitrogen atom directly attached in position 4
    • C07D475/08Heterocyclic compounds containing pteridine ring systems with a nitrogen atom directly attached in position 4 with a nitrogen atom directly attached in position 2
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D475/00Heterocyclic compounds containing pteridine ring systems
    • C07D475/06Heterocyclic compounds containing pteridine ring systems with a nitrogen atom directly attached in position 4

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrrole Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Claims (4)

1. Förfarande för framställning av farmakologiskt värdefulla 2-piperazinopteridiner med formeln I R1 N N N N- H (I) R2 där Rl är fenyläiky1amino-» dialkylaminogrupp, piperidino-, morfo-lino-, tiomorfolino- eller 1-oxidotiomorfolinogrupp, R2 är dialkylamino-, piperidino-, morfolino-, tiomorfolino-eller 1-oxidotiomorfolinogrupp och R3 är halogenatom, alkoxi-alkyltio-, fenylalkoxi- eller fenylalkyltiogrupp, varvid alkyldelen i respektive fall kan innehalla 1-3 kolatomer, och deras syraadditionssalter, speciellt deras fysiologiskt lampiiga syraadditionssalter med oorganiska eller organiska syror, kännetecknat därav, att a) för framställning av föreningar med den allmänna formeln I, där R3 är en halogenatom, bringas en förening med den allmänna formeln II Rlx^NYN^Z2 I an Rt A n R2 där Rl och R2 avser samma som ovan, 23 80454 R'3 är halogenatom och Z2 är en nukleofiliskt utbytbar grupp, sasom en halogenatom, att reagera med et piperazin med den allmänna formeln II H - N N - H (III) eller b) för framställning av föreningar med den allmänna formeln I, där R3 är alkoxi-, alkylmerkapto-, fenylalkoxi- eller fenyl-alkylmerkaptogrupp, brlngas en förening med den allmänna formeln IV R, . ^ N Nv /N N- H Ύ Y z3^n *2 där R^ och R2 avser samma som ovan och Z3 är en nukloefiliskt utbytbar grupp, sasom en halogenatom, att reagera med en förening med den allmänna formeln V R31 - H (V) där R31 eventuellt är en med fenylgrupp substituerad alkoxi- eller alkylmerkaptogrupp, varvid alkyldelen respektive innehaller 1-3 kolatomer, eller omsättes med dennas aikaiisalt och därefter vid behov överföres en sl erhallen förening med den 24 80454 allmänna formeln I till sitt syraadditionssalt, speciellt till sitt fysiologiskt lämpliga syraadditionssalt med en oorganisk eller organisk syra.
2. Förfarande enligt patentkravet 1, kännetecknat därav, att den framställda föreningen med formeln I Mr 6-bensyltio-4,7-dimorfolino-2-piperazino-pteridin eller dess syraadditionssalt.
3. Förfarande enligt patentkravet 1, kännetecknat därav, att den framställda föreningen med formeln i Mr 6-klor- 4,7-bis-(dimetylamino)-2-piperazino-pteridin eller dess syraadditionssalt.
4. Förfarande enligt patentkravet 1, kännetecknat därav, att den framställda föreningen med formeln I Mr 6-bensyltio-4,7-bis-(dimetylamino)-2-piperazino-pteridin eller dess syraadditionssalt. i!
FI842622A 1983-07-02 1984-06-29 Förfarande för framställning av farmakologiskt värdefulla 2-piperazino -pteridiner FI80454C (sv)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3323932 1983-07-02
DE19833323932 DE3323932A1 (de) 1983-07-02 1983-07-02 Neue 2-piperazino-pteridine, verfahren zu ihrer herstellung und diese verbindung enthaltende arzneimittel

Publications (4)

Publication Number Publication Date
FI842622A0 FI842622A0 (fi) 1984-06-29
FI842622A FI842622A (fi) 1985-01-03
FI80454B true FI80454B (fi) 1990-02-28
FI80454C FI80454C (sv) 1990-06-11

Family

ID=6203017

Family Applications (1)

Application Number Title Priority Date Filing Date
FI842622A FI80454C (sv) 1983-07-02 1984-06-29 Förfarande för framställning av farmakologiskt värdefulla 2-piperazino -pteridiner

Country Status (17)

Country Link
EP (1) EP0134922B1 (sv)
JP (1) JPS6025991A (sv)
AT (1) ATE39253T1 (sv)
AU (1) AU565105B2 (sv)
CA (1) CA1233179A (sv)
DD (1) DD229990A5 (sv)
DE (2) DE3323932A1 (sv)
DK (1) DK159113C (sv)
ES (2) ES8503352A1 (sv)
FI (1) FI80454C (sv)
GB (1) GB2143232B (sv)
HU (1) HU190932B (sv)
IL (1) IL72265A (sv)
NO (1) NO160920C (sv)
NZ (1) NZ208725A (sv)
PH (1) PH22493A (sv)
ZA (1) ZA844968B (sv)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3445298A1 (de) * 1984-12-12 1986-06-12 Dr. Karl Thomae Gmbh, 7950 Biberach Neue pteridine, verfahren zu ihrer herstellung und deren verwendung als zwischenprodukte oder als arzneimittel
DE3540952C2 (de) * 1985-11-19 1997-08-14 Thomae Gmbh Dr K 2-Piperazino-pteridine, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel
US7276506B2 (en) 1998-12-28 2007-10-02 4 Aza Bioscience Nv Immunosuppressive effects of pteridine derivatives
DE10202468A1 (de) * 2002-01-23 2004-09-30 Faustus Forschungs Cie. Translational Cancer Research Gmbh Pteridinderivate, Verfahren zu deren Herstellung und ihre Verwendung
ES2295897T3 (es) * 2003-08-29 2008-04-16 4 Aza Ip Nv Efectos inmunodepresores de derivados de pteridina.
GB2407089A (en) * 2003-10-17 2005-04-20 4 Aza Bioscience Nv Pteridine derivatives
DE102004057645A1 (de) 2004-11-29 2006-06-01 Boehringer Ingelheim Pharma Gmbh & Co. Kg Substituierte Pteridine zur Behandlung von entzündlichen Erkrankungen
DE102004057595A1 (de) * 2004-11-29 2006-06-08 Boehringer Ingelheim Pharma Gmbh & Co. Kg Substituierte Pteridine zur Behandlung von entzündlichen Erkrankungen
DE102004057594A1 (de) 2004-11-29 2006-06-08 Boehringer Ingelheim Pharma Gmbh & Co. Kg Substitueirte Pteridine zur Behandlung von entzündlichen Erkrankungen
DE102004057618A1 (de) 2004-11-29 2006-06-01 Boehringer Ingelheim Pharma Gmbh & Co. Kg Substituierte Pteridine zur Behandlung von entzündlichen Erkrankungen
EP2032585B1 (de) 2006-05-24 2014-07-23 Boehringer Ingelheim International GmbH Substituierte pteridine als therapeutika
WO2007135027A1 (de) * 2006-05-24 2007-11-29 Boehringer Ingelheim International Gmbh Substituierte pteridine, die mit einem viergliedrigen heterocyclus substituiert sind
WO2008003149A2 (en) * 2006-07-06 2008-01-10 Gilead Sciences , Inc. Substituted pteridines for the treatment and prevention of viral infections
WO2008009078A2 (en) 2006-07-20 2008-01-24 Gilead Sciences, Inc. 4,6-dl- and 2,4,6-trisubstituted quinazoline derivatives useful for treating viral infections
WO2008009079A2 (en) 2006-07-20 2008-01-24 Gilead Sciences, Inc. Substituted pteridines useful for the treatment and prevention of viral infections
EP3722297A1 (en) 2015-03-04 2020-10-14 Gilead Sciences, Inc. Toll-like receptor modulating 4,6-diamino-pyrido[3,2-d]pyrimidine compounds
EP3507288B1 (en) 2016-09-02 2020-08-26 Gilead Sciences, Inc. 4,6-diamino-pyrido[3,2-d]pyrimidine derivaties as toll like receptor modulators
PL3507276T3 (pl) 2016-09-02 2022-02-21 Gilead Sciences, Inc. Związki modulatory receptorów toll-podobnych
TWI751516B (zh) 2019-04-17 2022-01-01 美商基利科學股份有限公司 類鐸受體調節劑之固體形式
TWI751517B (zh) 2019-04-17 2022-01-01 美商基利科學股份有限公司 類鐸受體調節劑之固體形式
TW202115056A (zh) 2019-06-28 2021-04-16 美商基利科學股份有限公司 類鐸受體調節劑化合物的製備方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2940972A (en) * 1957-06-27 1960-06-14 Thomae Gmbh Dr K Tri-and tetra-substituted pteridine derivatives
FR1352111A (fr) * 1962-01-25 1964-02-14 Lumiere Lab Triamino ptéridines et leur préparation

Also Published As

Publication number Publication date
DK316284D0 (da) 1984-06-28
ES537785A0 (es) 1985-10-16
EP0134922B1 (de) 1988-12-14
NO160920C (no) 1989-06-14
IL72265A0 (en) 1984-10-31
NO160920B (no) 1989-03-06
NO842631L (no) 1985-01-03
ES533298A0 (es) 1985-02-16
FI80454C (sv) 1990-06-11
AU3009284A (en) 1985-01-03
ZA844968B (en) 1986-03-26
HU190932B (en) 1986-12-28
FI842622A (fi) 1985-01-03
IL72265A (en) 1987-08-31
ES8601205A1 (es) 1985-10-16
GB2143232B (en) 1986-11-05
AU565105B2 (en) 1987-09-03
DK159113B (da) 1990-09-03
CA1233179A (en) 1988-02-23
DE3323932A1 (de) 1985-01-10
DK316284A (da) 1985-01-03
PH22493A (en) 1988-09-12
ATE39253T1 (de) 1988-12-15
HUT34487A (en) 1985-03-28
DK159113C (da) 1991-02-18
GB2143232A (en) 1985-02-06
DD229990A5 (de) 1985-11-20
JPS6025991A (ja) 1985-02-08
EP0134922A1 (de) 1985-03-27
GB8416682D0 (en) 1984-08-01
ES8503352A1 (es) 1985-02-16
DE3475620D1 (en) 1989-01-19
FI842622A0 (fi) 1984-06-29
NZ208725A (en) 1988-10-28

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Owner name: DR. KARL THOMAE GESELLSCHAFT MIT