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YU48973B - 3(2h)-piridazinon derivati i postupak za njihovo dobijanje - Google Patents

3(2h)-piridazinon derivati i postupak za njihovo dobijanje

Info

Publication number
YU48973B
YU48973B YU109292A YU109292A YU48973B YU 48973 B YU48973 B YU 48973B YU 109292 A YU109292 A YU 109292A YU 109292 A YU109292 A YU 109292A YU 48973 B YU48973 B YU 48973B
Authority
YU
Yugoslavia
Prior art keywords
substituent
hydrogen
alkyl
group
phenyl
Prior art date
Application number
YU109292A
Other languages
English (en)
Other versions
YU109292A (sr
Inventor
MГЎtyus Dr. PГ©ter
CzakГі KlГЎra
Varga IldikГі
JednГЎkovics Andrea
Papp Dr. ГЃgnes
BГіdi Dr. Ilona
Rabloczky Dr. György
VarrГі AndrГЎs
Jaszlits Dr.LГЎszlГі
MiklГіs Dr.AnikГі
LГ©vay Luca
Schmidt György
Fekete Dr. MГЎrton
KГјrthy MГЎria
SzemerГ©di Dr.Katalin
ZГЎra Dr.ErzsГ©bet
Original Assignee
Egis GyГіguszerguГЎr
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 Egis GyГіguszerguГЎr filed Critical Egis GyГіguszerguГЎr
Priority to YU109292A priority Critical patent/YU48973B/sh
Publication of YU109292A publication Critical patent/YU109292A/sh
Publication of YU48973B publication Critical patent/YU48973B/sh

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/14Oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/06Antiarrhythmics

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

3(2H)-piridazinon derivati opšte formule (I): naznačeni time, što R1 je vodonik; fenil; metil koji opciono nosi benziloksi supstituent; C2-4 alkil koji opciono nosi supstituet formule R8R9N-, gde R8 i R9 su nezavisno C1-4 alkil, ili R8 i R9 formiraju, zajedno sa susednim atomima azota, 6-članu heterocikličnu grupu koja opciono sadrži atom kiseonika ili grupu formule R10N-, gde R10 je C1-4 aklil koji opiciono sadrži fenoksi supstituent, ili C3-5 alkenil koji opciono nosi fenil supstituent, dalje pomenuti C1-4 alkil je opciono suspstituisan sa fenilom koji nosi metoksi ili metansulfonilamino supstituent; ili C3-5 alkenil koji opciono nosi fenil ili halofenil supstituent, A i B su vodonik, halogen ili grupa opšte formule (II), gde R2 i R3 su nezavisno vodonik ili C1-4 alkil, ili zajedno sa susednom-N-(CH2)nN-grupom formiraju piperazin ili homopiperazin prsten; R4 je vodonik, C1-4 alkil ili fenil; R5, R6 i R7 svaki su vodonik, C1-4 alkoksi ili amino koji opciono nosi metansulfonil supstituent; X je jednostruka valentna veza, atom kiseonika ili grupa formule-CH=CH; m je 0 ili 1, i n je 2 ili 3 uz uslov da A i B su uvek različiti, i ako jedan A i B je vodonik ili halogen, drugi je grupa opšte formule (II), i njihove adicione soli kiseline. Prijava sadrži još 12 nezavisnih zahteva.
YU109292A 1991-12-20 1992-12-18 3(2h)-piridazinon derivati i postupak za njihovo dobijanje YU48973B (sh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
YU109292A YU48973B (sh) 1991-12-20 1992-12-18 3(2h)-piridazinon derivati i postupak za njihovo dobijanje

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
HU914057A HU214320B (hu) 1991-12-20 1991-12-20 Eljárás új 3(2H)-piridazinon-származékok és ezeket tartalmazó gyógyszerkészítmények előállítására
YU109292A YU48973B (sh) 1991-12-20 1992-12-18 3(2h)-piridazinon derivati i postupak za njihovo dobijanje

Publications (2)

Publication Number Publication Date
YU109292A YU109292A (sr) 1996-01-09
YU48973B true YU48973B (sh) 2003-02-28

Family

ID=10966710

Family Applications (1)

Application Number Title Priority Date Filing Date
YU109292A YU48973B (sh) 1991-12-20 1992-12-18 3(2h)-piridazinon derivati i postupak za njihovo dobijanje

Country Status (22)

Country Link
US (1) US5395934A (sh)
JP (1) JP3165935B2 (sh)
KR (1) KR100234596B1 (sh)
CN (1) CN1088578A (sh)
AT (1) AT403282B (sh)
BE (1) BE1006223A4 (sh)
CA (1) CA2085796C (sh)
CH (1) CH684754A5 (sh)
CZ (1) CZ286039B6 (sh)
DE (1) DE4243381B4 (sh)
DK (1) DK152892A (sh)
ES (1) ES2108595B1 (sh)
FI (1) FI106374B (sh)
FR (1) FR2685329B1 (sh)
GB (1) GB2262526B (sh)
GR (1) GR1002281B (sh)
HU (1) HU214320B (sh)
NL (1) NL194966C (sh)
PL (1) PL172933B1 (sh)
RU (1) RU2130019C1 (sh)
YU (1) YU48973B (sh)
ZA (1) ZA929903B (sh)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5969017A (en) * 1996-10-31 1999-10-19 Merck & Co., Inc. Methods of treating or preventing cardiac arrhythmia
US5935945A (en) * 1996-10-31 1999-08-10 Merck & Co., Inc. Methods of treating or preventing cardiac arrhythmia
CA2334220A1 (en) 1998-06-05 1999-12-16 Egis Gyogyszergyar Rt. Process for the preparation of a 3(2h)-pyridazinone- 4-substituted amino- 5-chloro- derivative
ES2162731B1 (es) * 1999-06-04 2003-02-16 Faes Fabrica Espanola De Produ Nuevas arilpiperacilnilalquil-3(2h)-piridacinonas.
WO2001034151A1 (en) * 1999-11-11 2001-05-17 Fred Hutchinson Cancer Research Center Novel topoisomerase poisons for the treatment of proliferative disorders
US7173063B1 (en) 2000-11-10 2007-02-06 Fred Hutchinson Cancer Research Center Topoisomerase poisons for the treatment of proliferative disorders
HUP0103064A3 (en) * 2001-07-26 2005-06-28 Egis Gyogyszergyar Nyilvanosan Polymorphic form of 5-chloro-4-(3-{[2-(3,4-dimethoxy-phenyl)-ethyl]-methyl-amino]-propylamino)-3-(2h)-piridazinone fumarate, its use, process for its preparation and pharmaceutical compositions containing it
HU227237B1 (en) * 2001-09-27 2010-12-28 Egis Gyogyszergyar Nyilvanosan Muekoedoe Reszvenytarsasag Substituted alkylpyridazinone derivatives, process for their preparation, pharmaceutical compositions containing them
CA2474239A1 (en) * 2002-01-18 2003-07-24 Pharmacia Corporation Substituted pyridazinones as inhibitors of p38
HU227181B1 (en) * 2002-09-11 2010-09-28 Egis Gyogyszergyar Nyilvanosan Use of 5-chloro-4-[3-[n-[2-(3,4-dimethoxyphenyl)ethyl)]-n-methylamino]-propylamino]-3-(2h)-pyridazinone for producing pharmaceutical compositions having metabolic modulator effect
WO2011062437A2 (ko) * 2009-11-20 2011-05-26 에스케이케미칼주식회사 고나도트로핀 방출 호르몬 수용체 길항제, 이의 제조방법 및 이를 함유하는 약제학적 조성물
WO2011097553A1 (en) * 2010-02-08 2011-08-11 Allergan, Inc. Pyridazine derivatives useful as cannabinoid - 2 agonists
FR2969606B1 (fr) * 2010-12-22 2013-01-11 Pf Medicament Derives de diarylpyridazinones, leur preparation et leur application en therapeutique humaine
RU2455004C1 (ru) * 2011-04-01 2012-07-10 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Ярославский государственный технический университет" (ФГБОУ ВПО "ЯГТУ") Способ получения сульфохлоридов ряда 6-арилпиридазин-3(2н)-онов

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1285235A (fr) * 1960-01-21 1962-02-23 Ciba Geigy Procédé de préparation de nouvelles diazines, notamment de 1-aryl-3-r-5-r'pyridazones-(6) dans lesquelles r représente un hydroxyle aliphatiquement éthérifié et r' représente un groupe n-(beta-aryl-éthyl)-pipérazino
US4088764A (en) * 1973-12-27 1978-05-09 Cassella Farbwerke Mainkur Aktiengesellschaft Pharmaceutically active derivatives of 1-phenoxy-3-amino-propan-2-ol
DE3048487A1 (de) * 1980-12-22 1982-07-29 Cassella Ag, 6000 Frankfurt Basisch substituierte pyridazine, ihre herstellung und ihre verwendung
JPH0641454B2 (ja) * 1985-02-27 1994-06-01 日産化学工業株式会社 ピリダジノン誘導体
US4892947A (en) * 1985-04-27 1990-01-09 Nissan Chemical Industries Ltd. 3(2H)Pyridazinone, process for its preparation and anti-allergic agent containing it
US4992433A (en) * 1987-11-23 1991-02-12 Janssen Pharmaceutica N.V. Novel pyridazinamine derivatives
MY104343A (en) * 1987-11-23 1994-03-31 Janssen Pharmaceutica Nv Novel pyridizinamine deravatives
AU610204B2 (en) * 1988-03-17 1991-05-16 Institut Fiziologicheski Aktivnykh Veschestv Akademii Nauk SSSR Method of sterilizing anthers utilizing derivatives of phosphoric acid
IE62890B1 (en) * 1988-12-06 1995-03-08 Hafslund Nycomed Pharma New piperazinylalkyl-3(2h)-pyridazinones process for the preparation thereof and the use thereof as agents lowering blood pressure
DE3902316A1 (de) * 1989-01-26 1990-08-02 Lentia Gmbh Neue piperazinylalkyl-3(2h)-pyridazinone, verfahren zu ihrer herstellung und ihre verwendung als blutdrucksenkende mittel

Also Published As

Publication number Publication date
AU652304B2 (en) 1994-08-18
ES2108595B1 (es) 1998-08-16
AU3031792A (en) 1993-06-24
HU914057D0 (en) 1992-03-30
PL297070A1 (en) 1994-03-07
RU2130019C1 (ru) 1999-05-10
AT403282B (de) 1997-12-29
CA2085796C (en) 2000-08-08
BE1006223A4 (fr) 1994-06-14
JP3165935B2 (ja) 2001-05-14
GR920100570A (el) 1993-08-31
DK152892A (da) 1993-06-21
NL194966C (nl) 2003-09-02
HUT62865A (en) 1993-06-28
KR100234596B1 (ko) 1999-12-15
CZ380992A3 (en) 1993-09-15
NL194966B (nl) 2003-05-01
HU214320B (hu) 1998-03-02
GB2262526B (en) 1995-07-26
FI925807A (fi) 1993-06-21
FI925807A0 (fi) 1992-12-21
CN1088578A (zh) 1994-06-29
CZ286039B6 (cs) 1999-12-15
NL9202210A (nl) 1993-07-16
FR2685329B1 (fr) 1994-12-02
YU109292A (sr) 1996-01-09
ATA253592A (de) 1997-05-15
GR1002281B (el) 1996-05-02
GB9226601D0 (en) 1993-02-17
PL172933B1 (pl) 1997-12-31
US5395934A (en) 1995-03-07
ZA929903B (en) 1993-06-24
DK152892D0 (da) 1992-12-21
CH684754A5 (de) 1994-12-15
DE4243381A1 (sh) 1993-06-24
JPH05255276A (ja) 1993-10-05
CA2085796A1 (en) 1993-06-21
FI106374B (fi) 2001-01-31
FR2685329A1 (fr) 1993-06-25
DE4243381B4 (de) 2005-07-28
GB2262526A (en) 1993-06-23
ES2108595A1 (es) 1997-12-16

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