NO20015966L - Tricyclic analgesics - Google Patents

Tricyclic analgesics

Info

Publication number
NO20015966L
NO20015966L NO20015966A NO20015966A NO20015966L NO 20015966 L NO20015966 L NO 20015966L NO 20015966 A NO20015966 A NO 20015966A NO 20015966 A NO20015966 A NO 20015966A NO 20015966 L NO20015966 L NO 20015966L
Authority
NO
Norway
Prior art keywords
alkyl
hydrogen
alkenyl
cycloalkyl
tricyclic
Prior art date
Application number
NO20015966A
Other languages
Norwegian (no)
Other versions
NO20015966D0 (en
Inventor
Alain Calvet
Henri Jacobelli
Jocelyne Puaud
Francois Joseph Roman
Jacques Hamon
Agnes Grouhel
Original Assignee
Warner Lambert Co
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 Warner Lambert Co filed Critical Warner Lambert Co
Publication of NO20015966D0 publication Critical patent/NO20015966D0/en
Publication of NO20015966L publication Critical patent/NO20015966L/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/20Spiro-condensed ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/438The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
    • 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
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A61P29/02Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Tricyklisk forbindelse med formel I hvori R1 er hydrogen eller hydroksy;R2er hydrogen eller hydroksy; eller R1 og R2 sammen er oksygen ; A er en binding, CH2, CH CH3, CH2 CH2 eller C(CH3)2; R3 og R4 er like eller forskjellige og er hydrogen, halogen, C|-C6-alkyl, C|- C4-alkoksy, trifluormetyl, NO2, COR6, COOR6 eller NR5R7, hvor R6 og R7 er like eller forskjellige og er hydrogen, C|-C&-alkyl eller benzyl ; R5 er hydrogen, C|.6 alkyl, C2.6 alkenyl, C3.6 cykloalkyl, (O=C)-C|.5 alkyl, (O=C)-C2.6 alkenyl, (O=C)-C3-6 cykloalkyl, hvor nevnte alkyl, alkenyl og cykloalkylgrupper kan være substituert med l, 2 eller 3 grupper valgt fra halogen, Cj-Cb-cykloalkyl, fenyl eller substituert fenyl, og salter derav, er spesielt anvendelige for behandling av, blant andre indikasjoner, av nevropatisk smerte og andre CNS-fortyrrelser.Tricyclic compound of formula I wherein R 1 is hydrogen or hydroxy; R 2 is hydrogen or hydroxy; or R1 and R2 together are oxygen; A is a bond, CH 2, CH CH 3, CH 2 CH 2 or C (CH 3) 2; R 3 and R 4 are the same or different and are hydrogen, halogen, C 1 -C 6 alkyl, C 1 -C 4 alkoxy, trifluoromethyl, NO 2, COR 6, COOR 6 or NR 5 R 7, where R 6 and R 7 are the same or different and are hydrogen, C -C 1-4 alkyl or benzyl; R 5 is hydrogen, C 1-6 alkyl, C 2-6 alkenyl, C 3-6 cycloalkyl, (O = C) -C 1-5 alkyl, (O = C) -C 2-6 alkenyl, (O = C) -C 3 -6 cycloalkyl, wherein said alkyl, alkenyl and cycloalkyl groups may be substituted with 1, 2 or 3 groups selected from halogen, C , of neuropathic pain and other CNS disorders.

NO20015966A 1999-06-07 2001-12-06 Tricyclic analgesics NO20015966L (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13786899P 1999-06-07 1999-06-07
PCT/EP2000/005783 WO2000075116A2 (en) 1999-06-07 2000-06-07 Tricyclic analgesics

Publications (2)

Publication Number Publication Date
NO20015966D0 NO20015966D0 (en) 2001-12-06
NO20015966L true NO20015966L (en) 2001-12-06

Family

ID=22479397

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20015966A NO20015966L (en) 1999-06-07 2001-12-06 Tricyclic analgesics

Country Status (21)

Country Link
EP (1) EP1235808A2 (en)
JP (1) JP2003513006A (en)
KR (1) KR20020010923A (en)
CN (1) CN1635998A (en)
AP (1) AP2001002356A0 (en)
AU (1) AU6428400A (en)
BG (1) BG106162A (en)
BR (1) BR0011427A (en)
CA (1) CA2376076A1 (en)
EA (1) EA200101117A1 (en)
HR (1) HRP20010913A2 (en)
HU (1) HUP0203317A2 (en)
IL (1) IL146755A0 (en)
IS (1) IS6175A (en)
MA (1) MA26795A1 (en)
MX (1) MXPA01012694A (en)
NO (1) NO20015966L (en)
PL (1) PL357340A1 (en)
SK (1) SK17512001A3 (en)
TR (1) TR200103531T2 (en)
WO (1) WO2000075116A2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030045449A1 (en) * 2001-08-15 2003-03-06 Pfizer, Inc. Pharmaceutical combinations for the treatment of neurodegenerative diseases
FR2915099B1 (en) * 2007-04-19 2009-06-05 Sanofi Aventis Sa USE OF 4-CYCLOPROPYLMETHOXY-N- (3,5-DICHLORO-1-OXYDO-PYRIDIN-4-YL) -5- (METHOXY) PYRIDINE-2-CARBOXAMIDE FOR THE TREATMENT OF CRANIAL TRAUMATISM
WO2012106499A1 (en) * 2011-02-02 2012-08-09 Vertex Pharmaceuticals Incorporated Pyrrolopyrazine-spirocyclic piperidine amides as modulators of ion channels
GB201416346D0 (en) * 2014-09-16 2014-10-29 Shire Internat Gmbh Spirocyclic derivatives
CN115872873A (en) * 2022-12-29 2023-03-31 上海泰坦科技股份有限公司 Recrystallization purification method of bis (2-bromoethyl) amine hydrobromide

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8917069D0 (en) * 1989-07-26 1989-09-13 Merck Sharp & Dohme Therapeutic agents
IL96507A0 (en) * 1989-12-08 1991-08-16 Merck & Co Inc Nitrogen-containing spirocycles and pharmaceutical compositions containing them
DK0681571T3 (en) * 1993-01-28 1998-11-23 Merck & Co Inc Spiro-substituted azacyclic compounds as tachykinin receptor antagonists
US5439914A (en) * 1994-02-18 1995-08-08 Merck & Co., Inc. Spirocycles
WO1998025604A1 (en) * 1996-12-13 1998-06-18 Merck & Co., Inc. Spiro-substituted azacycles as modulators of chemokine receptor activity
US6013644A (en) * 1997-12-12 2000-01-11 Merck & Co., Inc. Spiro-substituted azacycles as modulators of chemokine receptor activity

Also Published As

Publication number Publication date
IS6175A (en) 2001-11-23
WO2000075116A2 (en) 2000-12-14
MA26795A1 (en) 2004-12-20
CA2376076A1 (en) 2000-12-14
HRP20010913A2 (en) 2003-04-30
AU6428400A (en) 2000-12-28
AP2001002356A0 (en) 2001-12-31
MXPA01012694A (en) 2003-10-15
CN1635998A (en) 2005-07-06
HUP0203317A2 (en) 2003-02-28
NO20015966D0 (en) 2001-12-06
TR200103531T2 (en) 2002-06-21
BR0011427A (en) 2002-03-26
JP2003513006A (en) 2003-04-08
EA200101117A1 (en) 2002-06-27
KR20020010923A (en) 2002-02-06
BG106162A (en) 2002-05-31
SK17512001A3 (en) 2002-11-06
WO2000075116A3 (en) 2002-07-04
PL357340A1 (en) 2004-07-26
EP1235808A2 (en) 2002-09-04
IL146755A0 (en) 2002-07-25

Similar Documents

Publication Publication Date Title
HUP0000079A2 (en) Indane or dihydroindole derivatives
HRP20020175B1 (en) N-heterocyclikc derivatives as nos inhibitors
MY129796A (en) Novel anti-inflammatory androstane derivatives
TR200003332T2 (en) Method to produce isoxazolin-3-yl-acyl benzene
NO982913L (en) Quinoline and quinazoline compounds useful in therapy
HUP0300268A2 (en) Herbicidal benzoylpyrazole derivatives, compositions containing the same and their use
SG49984A1 (en) Oximesulfonic acid esters and the use thereof as latent sulfonic acids
IS4588A (en) Benzimidazole compounds, pharmaceutical compositions containing the compounds and their use
NO20053960L (en) Piperidine-benzenesulfonamide
DE60317884D1 (en) SODIUM CHANNEL BLOCKER
HUP9903836A2 (en) New process of preparing phenyl substituted 2(5h)-furanones having cox-2 inhibitor activity
CO4700452A1 (en) DERIVATIVES OF INDOL
ATE182889T1 (en) BICYCLIC AMIDEINE DERIVATIVES AS NO-SYNTHETASE INHIBITORS
NO20015966L (en) Tricyclic analgesics
BG105299A (en) Substituted amidazo[1,2a]azines as selective inhibitors of cox-2
DE59808284D1 (en) CYCLOALKYLALCANCARBOXYLIC ACID AMIDES, THEIR PRODUCTION AND USE
ATE121385T1 (en) UREA DERIVATIVES, THEIR PRODUCTION AND THEIR USE IN THERAPY.
ES2191341T3 (en) DERIVATIVES OF 2-PHENOXIANILINE.
FI942928A (en) Aromatic esters of phenylene alkanoates as inhibitors of human neutrophil elastase
ATE121294T1 (en) INDANDERIVATES.
DK1335913T3 (en) Process for the preparation of pantoprazole and its intermediates
ATE246703T1 (en) ORAL ACTIVE 7-ALPHA-ALKYL ANDROGENS
NO995289L (en) Benzimidazole derivatives
EA200401099A1 (en) Derivatives of Heterocyclic Amide
IT1255207B (en) PHARMACEUTICAL COMPOSITIONS WITH ANTI-AGGREGATING AND VASODILATING ACTIVITY

Legal Events

Date Code Title Description
FC2A Withdrawal, rejection or dismissal of laid open patent application