FI63397C - Foerfarande foer framstaellning av terapeutiskt anvaendbara 3-1-pyrazolyl)-pyridazinderivat - Google Patents

Foerfarande foer framstaellning av terapeutiskt anvaendbara 3-1-pyrazolyl)-pyridazinderivat Download PDF

Info

Publication number
FI63397C
FI63397C FI782237A FI782237A FI63397C FI 63397 C FI63397 C FI 63397C FI 782237 A FI782237 A FI 782237A FI 782237 A FI782237 A FI 782237A FI 63397 C FI63397 C FI 63397C
Authority
FI
Finland
Prior art keywords
pyrazolyl
alkyl
nhr
group
pyridazine
Prior art date
Application number
FI782237A
Other languages
English (en)
Finnish (fi)
Other versions
FI63397B (fi
FI782237A (fi
Inventor
Geza Szilagyi
Endre Kasztreiner
Laszlo Tardos
Edit Kosa
Laszlo Jaszlits
Gyoergy Cseh
Nee Szabo Ilona Kovacs
Pal Tolnay
Sandor Elek
Istvan Elekes
Istvan Polgari
Original Assignee
Richter Gedeon Vegyeszet
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 Richter Gedeon Vegyeszet filed Critical Richter Gedeon Vegyeszet
Publication of FI782237A publication Critical patent/FI782237A/fi
Publication of FI63397B publication Critical patent/FI63397B/fi
Application granted granted Critical
Publication of FI63397C publication Critical patent/FI63397C/fi

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • 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
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
FI782237A 1977-10-25 1978-07-13 Foerfarande foer framstaellning av terapeutiskt anvaendbara 3-1-pyrazolyl)-pyridazinderivat FI63397C (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
HUGO001381 1977-10-25
HU77GO1381A HU176100B (en) 1977-10-25 1977-10-25 Process for preparing new 3-/1-pyrazolyl/-pyridazine derivatives

Publications (3)

Publication Number Publication Date
FI782237A FI782237A (fi) 1979-04-26
FI63397B FI63397B (fi) 1983-02-28
FI63397C true FI63397C (fi) 1983-06-10

Family

ID=10996838

Family Applications (1)

Application Number Title Priority Date Filing Date
FI782237A FI63397C (fi) 1977-10-25 1978-07-13 Foerfarande foer framstaellning av terapeutiskt anvaendbara 3-1-pyrazolyl)-pyridazinderivat

Country Status (24)

Country Link
US (1) US4224325A (ru)
JP (1) JPS5461187A (ru)
AT (1) AT359076B (ru)
AU (1) AU525814B2 (ru)
BE (1) BE868987A (ru)
CA (1) CA1090337A (ru)
CH (1) CH637951A5 (ru)
CS (1) CS217964B2 (ru)
DD (1) DD139848A5 (ru)
DE (1) DE2831072A1 (ru)
DK (1) DK317678A (ru)
ES (1) ES471779A1 (ru)
FI (1) FI63397C (ru)
FR (1) FR2407211A1 (ru)
GB (1) GB2007644B (ru)
HU (1) HU176100B (ru)
IL (1) IL55120A (ru)
IT (1) IT1097156B (ru)
NL (1) NL7807572A (ru)
NO (1) NO149354C (ru)
PL (2) PL115063B1 (ru)
SE (1) SE437988B (ru)
SU (3) SU847920A3 (ru)
YU (1) YU169878A (ru)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4302456A (en) * 1977-04-13 1981-11-24 The Upjohn Company Process for therapeutic treatment
US4302457A (en) * 1977-04-13 1981-11-24 The Upjohn Company Process for therapeutic treatment
DE2935359A1 (de) * 1979-09-01 1981-03-26 Basf Ag, 67063 Ludwigshafen 6-imidazolyl-3-hydrazino-pyridazine
US4304775A (en) * 1979-12-13 1981-12-08 Sterling Drug Inc. 3-Hydrazino-6-(pyridinyl) pyridazines and cardiotonic use thereof
US4503056A (en) * 1982-03-02 1985-03-05 Abbott Laboratories 1-(Pyridazinyl)pyrazoline derivatives
US5001125A (en) * 1984-03-26 1991-03-19 Janssen Pharmaceutica N.V. Anti-virally active pyridazinamines

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1220428B (de) 1960-03-25 1966-07-07 Takeda Pharmaceutical Verfahren zur Herstellung von 2-Pyrazolyl-(1')-pyrimidinderivaten und deren Salzen
JPS5831347B2 (ja) * 1975-09-05 1983-07-05 中外製薬株式会社 ピラゾリルピリダジンユウドウタイノ セイホウ
HU175471B (hu) * 1977-06-13 1980-08-28 Gyogyszerkutato Intezet Sposob poluchenija novykh proizvodnykh 3-skobka-1-pirazolil-skobka zakryta-piridazina

Also Published As

Publication number Publication date
JPS5527063B2 (ru) 1980-07-17
ATA509278A (de) 1980-03-15
DD139848A5 (de) 1980-01-23
SE437988B (sv) 1985-03-25
PL118799B1 (en) 1981-10-31
HU176100B (en) 1980-12-28
FI63397B (fi) 1983-02-28
FR2407211A1 (fr) 1979-05-25
FI782237A (fi) 1979-04-26
FR2407211B1 (ru) 1982-09-03
SE7807822L (sv) 1979-04-26
GB2007644B (en) 1982-03-10
AU525814B2 (en) 1982-12-02
IL55120A0 (en) 1978-09-29
DE2831072A1 (de) 1979-05-10
US4224325A (en) 1980-09-23
NL7807572A (nl) 1979-04-27
AT359076B (de) 1980-10-27
BE868987A (fr) 1979-01-15
IL55120A (en) 1982-05-31
PL208409A1 (ru) 1980-02-25
YU169878A (en) 1983-01-21
NO149354B (no) 1983-12-27
CH637951A5 (de) 1983-08-31
JPS5461187A (en) 1979-05-17
SU856385A3 (ru) 1981-08-15
NO149354C (no) 1984-04-04
PL115063B1 (en) 1981-03-31
SU845786A3 (ru) 1981-07-07
IT7825681A0 (it) 1978-07-14
CA1090337A (en) 1980-11-25
PL218031A1 (ru) 1980-07-14
DK317678A (da) 1979-04-26
ES471779A1 (es) 1979-10-01
NO782446L (no) 1979-04-26
GB2007644A (en) 1979-05-23
AU3799778A (en) 1980-01-17
IT1097156B (it) 1985-08-26
CS217964B2 (en) 1983-02-25
SU847920A3 (ru) 1981-07-15

Similar Documents

Publication Publication Date Title
Dunkley et al. Synthesis and biological evaluation of a novel phenyl substituted sydnone series as potential antitumor agents
FI64156B (fi) Foerfarande foer framstaellning av terapeutiskt anvaendbara 3-1-pyrazolyl)-pyridazinderivat
US20030229229A1 (en) Process for preparing indolinone derivatives
FI63397C (fi) Foerfarande foer framstaellning av terapeutiskt anvaendbara 3-1-pyrazolyl)-pyridazinderivat
Kamchonwongpaisan et al. Flexible diaminodihydrotriazine inhibitors of Plasmodium falciparum dihydrofolate reductase: Binding strengths, modes of binding and their antimalarial activities
JP2016196463A (ja) 純粋なエルロチニブ
TW201502124A (zh) 製備苯并咪唑衍生物之方法
CN111704646B (zh) 甾体类化合物及其制备方法和用途
RU2193554C2 (ru) Производные ароматических аминов, обладающих подавляющим оас действием, способ их получения и ингибитор ноас
Ibrahim et al. Design and synthesis of novel pyrazolo [3, 4-d] pyrimidin-4-one bearing quinoline scaffold as potent dual PDE5 inhibitors and apoptotic inducers for cancer therapy
WO2017114843A1 (en) Xanthine derivative inhibitors of bet proteins
CN115215847A (zh) 一类kras-sos1抑制剂、其制备方法及其应用
JP6987125B2 (ja) 新規2,4,6−三置換s−トリアジン化合物並びにその製造方法および使用
CN108997176B (zh) 一种4-氯-n-取代苯基-3-磺酰氨基苯甲酰胺类化合物及其制备和抗肿瘤应用
DK149810B (da) Analogifremgangsmaade til fremstilling af basisk substituerede 3-oxopyridaziner og deres fysiologisk acceptable syreadditionssalte
JPH07138238A (ja) 新規キナゾリン誘導体およびそれを有効成分とする抗腫瘍剤
WO2020017624A1 (ja) 抗がん剤
US10202349B2 (en) Asymmetric bis-acridines with antitumour activity and their uses
CS244653B2 (en) Production method of new pyridazinel-hydrazone derivatives
Eißmann et al. Synthesis and structural characterization of amino acid and peptide derivatives featuring N-(p-bromobenzoyl) substituents as promising connection unit for bio-inspired hybrid compounds
US6015811A (en) Antitumor Chrysene derivatives
WO2024144680A1 (en) Specific arylidene barbiturate derivative molecules for use as drug candidates in cancer treatment
Anisimova et al. Studies of Imidazo [1, 2-a] Benzimidazoles 32*. Synthesis and Properties of 2, 3-Dihydroimidazo-and 2, 3, 4, 10-Tetrahydropyrimido [1, 2-a] Benzimidazol-9 (10)-Ylacetic Acids
Moinet-Hedin et al. In vitro cytotoxicity of carbazole derivatives. V. 9-Halogeno-substituted 5, 11-dimethyl-6H-pyrido [3, 2-b] carbazoles
CN116283929B (zh) 诱导egfr降解的化合物及其应用

Legal Events

Date Code Title Description
MM Patent lapsed

Owner name: RICHTER GEDEON VEGYESZETI GYAR R.T.