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FI83220B - Foerfarande foer framstaellning av terapeutiskt anvaendbara 1,3-dimetyl-1h-purin-2,6-dionderivat. - Google Patents

Foerfarande foer framstaellning av terapeutiskt anvaendbara 1,3-dimetyl-1h-purin-2,6-dionderivat. Download PDF

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Publication number
FI83220B
FI83220B FI853763A FI853763A FI83220B FI 83220 B FI83220 B FI 83220B FI 853763 A FI853763 A FI 853763A FI 853763 A FI853763 A FI 853763A FI 83220 B FI83220 B FI 83220B
Authority
FI
Finland
Prior art keywords
dimethyl
formula
purine
compound
dione
Prior art date
Application number
FI853763A
Other languages
English (en)
Finnish (fi)
Other versions
FI853763L (fi
FI83220C (sv
FI853763A0 (fi
Inventor
Ludo Edmond Josephine Kennis
Jan Vandenberk
Jozef Martin Boey
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of FI853763A0 publication Critical patent/FI853763A0/fi
Publication of FI853763L publication Critical patent/FI853763L/fi
Application granted granted Critical
Publication of FI83220B publication Critical patent/FI83220B/fi
Publication of FI83220C publication Critical patent/FI83220C/sv

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/08Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Anesthesiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Indole Compounds (AREA)

Claims (2)

1 N
10 -N-Alk-N (1) 1 $ R 15 i vilken formel Alk är C2.4-alkandiyl, R är väte, hydroxi, C1.4-alkyl, halogen eller metoxi och den streckade linjen är en eventuell bindning mellan kolatomerna 3 och 4, k ä n -netecknat därav, att en förening med formeln 20 CH, I 3 °γΝ YN^ {II) CH3-N -N-Alk-W 25 0 där Alk betecknar samma som ovan och W är en reaktiv av-gäende grupp, företrädesvis halogen, omsätts med ett pipe-rldinderivat med formeln 30 R II 17 83220 där R och den streckade Iinjen betecknar samma som ovan, företrädesvis i ett i förhällande till reaktionen inert lösningsmedel; och, om sä önskas, omvandlas en erhällen förening med formeln I pä och i för sig känt sätt tili en 5 annan förening med formeln I och/eller omvandlas en förening med formeln I tili ett farmaceutiskt godtagbart syra-additionssalt genom användning av en lämplig syra eller omvandlas ett syraadditionssalt tili en fri bas genom användning av en alkali och/eller omvandlas en förening med 10 formeln I tili en stereokemisk isomerform.
1. Förfarande för framställning av nya terapeutiskt användbara 1,3-dimetyl-lH-purin-2,6-dionderivat med for-5 mein I och farmaceutiskt godtagbara syraadditionssalter därav, CH,
2. Förfarande enligt patentkravet 1 för framställ-ning av 7-[2-[4-(lH-indol-3-yl)-l-piperidinyl]etyl]-3,7-dihydro-1,3-dimetyl-lH-purin-2,6-dion eller ett farmaceutiskt godtagbart syraadditionssalt därav, k ä n n e -15 tecknat därav, att en förening med formeln II, där Alk är -CH2CH2- och W är klor, brom eller jod, omsätts med 3-(4-piperidinyl)-lH-indol i ett i förhällande tili reaktionen inert lösningsmedel eventuellt i närvaro av en bas och, om sä önskas, omvandlas den erhällna föreningen tili 20 ett farmaceutiskt godtagbart syraadditionssalt genom användning en lämplig syra eller omvandlas det erhällna sy-raadditionssaltet tili fri bas genom användninig av alka li.
FI853763A 1984-10-01 1985-09-30 Förfarande för framställning av terapeutiskt användbara 1,3-dimetyl-1H -purin-2,6-dionderivat FI83220C (sv)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US65656184 1984-10-01
US06/656,561 US4548939A (en) 1984-10-01 1984-10-01 1H-Indol-3-yl containing 1,3-dimethyl-1H-purine-2,6-diones

Publications (4)

Publication Number Publication Date
FI853763A0 FI853763A0 (fi) 1985-09-30
FI853763L FI853763L (fi) 1986-04-02
FI83220B true FI83220B (fi) 1991-02-28
FI83220C FI83220C (sv) 1991-06-10

Family

ID=24633577

Family Applications (1)

Application Number Title Priority Date Filing Date
FI853763A FI83220C (sv) 1984-10-01 1985-09-30 Förfarande för framställning av terapeutiskt användbara 1,3-dimetyl-1H -purin-2,6-dionderivat

Country Status (17)

Country Link
US (1) US4548939A (sv)
EP (1) EP0177087B1 (sv)
JP (1) JPH0653742B2 (sv)
CN (1) CN1011311B (sv)
AT (1) ATE60604T1 (sv)
AU (1) AU576386B2 (sv)
CA (1) CA1262348A (sv)
DE (1) DE3581577D1 (sv)
DK (1) DK163996C (sv)
ES (1) ES8609324A1 (sv)
FI (1) FI83220C (sv)
GR (1) GR852375B (sv)
IE (1) IE58747B1 (sv)
NO (1) NO162069C (sv)
NZ (1) NZ213498A (sv)
PT (1) PT81229B (sv)
ZA (1) ZA857553B (sv)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH648559A5 (de) * 1981-07-20 1985-03-29 Siegfried Ag Theophyllinderivate und verfahren zu deren herstellung.
US4742057A (en) * 1985-12-05 1988-05-03 Fujisawa Pharmaceutical Co., Ltd. Antiallergic thiazole compounds
AU611469B2 (en) * 1987-08-13 1991-06-13 Glaxo Group Limited Indole derivatives
GB8719167D0 (en) * 1987-08-13 1987-09-23 Glaxo Group Ltd Chemical compounds
DK733788A (da) * 1988-01-14 1989-07-15 Fujisawa Pharmaceutical Co Indolylpiperidinderivater og fremgangsmaade til fremstilling deraf
GB8819024D0 (en) * 1988-08-10 1988-09-14 Glaxo Group Ltd Chemical compounds
DE8817122U1 (de) * 1988-12-22 1993-02-04 Boehringer Ingelheim Kg, 55218 Ingelheim Neue Xanthinderivate mit Adenosinantogenistischer Wirkung
DK292A (da) * 1991-11-29 1992-01-02 Tanisake Kk Middel
DE4414113A1 (de) * 1994-04-22 1995-10-26 Merck Patent Gmbh 3-Indolylpiperidine
CN108042542A (zh) * 2007-06-22 2018-05-18 海德拉生物科学公司 用于治疗病症的方法和组合物
US8318728B2 (en) 2008-05-14 2012-11-27 Hydra Biosciences, Inc. Compounds and compositions for treating chemical warfare agent-induced injuries
WO2009140517A1 (en) 2008-05-14 2009-11-19 Hydra Biosciences, Inc. Compounds and compositions for treating chemical warfare agent-induced injuries

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2322470A1 (de) * 1973-05-04 1974-11-21 Boehringer Sohn Ingelheim Neue indolyl-piperidino-(bzw. 1,2,5,6tetrahydro-pyridyl-)butyrophenone und verfahren zu ihrer herstellung
FR2334358A1 (fr) * 1975-12-12 1977-07-08 Sogeras Nouveaux medicaments derives de l'indole
FR2362628A1 (fr) * 1976-08-26 1978-03-24 Roussel Uclaf Nouveaux derives du piperidyl-indole et leurs sels, procede de preparation et application a titre de medicaments
EP0011399A1 (en) * 1978-11-11 1980-05-28 FISONS plc N-substituted theophyllines, processes for their preparation and pharmaceutical compositions containing them
DE2922159A1 (de) * 1979-05-31 1980-12-04 Boehringer Mannheim Gmbh Neue xanthin-derivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
US4342870A (en) * 1980-03-28 1982-08-03 Janssen Pharmaceutica N.V. Novel 3-(1-piperidinylalkyl)-4H-pyrido[1,2-a]pyrimidin-4-one derivatives
US4426383A (en) * 1980-09-04 1984-01-17 Eisai Co., Ltd. Theophylline and theobromine derivatives
US4359468A (en) * 1981-02-25 1982-11-16 Boehringer Ingelheim Ltd. Antiallergic N-[4-(indolyl)-piperidino-alkyl]-benzimidazolones
US4443451A (en) * 1981-07-15 1984-04-17 Janssen Pharmaceutica N.V. Bicyclic pyrimidin-5-one derivatives
CH648559A5 (de) * 1981-07-20 1985-03-29 Siegfried Ag Theophyllinderivate und verfahren zu deren herstellung.

Also Published As

Publication number Publication date
EP0177087A2 (en) 1986-04-09
ES8609324A1 (es) 1986-07-16
NZ213498A (en) 1988-04-29
DK163996B (da) 1992-04-27
IE58747B1 (en) 1993-11-03
FI853763L (fi) 1986-04-02
JPH0653742B2 (ja) 1994-07-20
NO162069C (no) 1989-11-01
JPS6187681A (ja) 1986-05-06
AU576386B2 (en) 1988-08-25
EP0177087A3 (en) 1986-06-11
DK444085A (da) 1986-04-02
ATE60604T1 (de) 1991-02-15
ZA857553B (en) 1987-05-27
US4548939A (en) 1985-10-22
DK163996C (da) 1992-09-21
PT81229A (en) 1985-11-01
PT81229B (pt) 1987-11-30
AU4812485A (en) 1986-04-10
DK444085D0 (da) 1985-09-30
CA1262348A (en) 1989-10-17
NO162069B (no) 1989-07-24
ES547447A0 (es) 1986-07-16
EP0177087B1 (en) 1991-01-30
CN1011311B (zh) 1991-01-23
CN85105804A (zh) 1986-10-22
FI83220C (sv) 1991-06-10
FI853763A0 (fi) 1985-09-30
NO853856L (no) 1986-04-02
IE852403L (en) 1986-04-01
GR852375B (sv) 1986-01-31
DE3581577D1 (de) 1991-03-07

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Owner name: JANSSEN PHARMACEUTICA N.V.