NO20073758L - 2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl-piperidines used as CGRP antagonists - Google Patents

2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl-piperidines used as CGRP antagonists

Info

Publication number
NO20073758L
NO20073758L NO20073758A NO20073758A NO20073758L NO 20073758 L NO20073758 L NO 20073758L NO 20073758 A NO20073758 A NO 20073758A NO 20073758 A NO20073758 A NO 20073758A NO 20073758 L NO20073758 L NO 20073758L
Authority
NO
Norway
Prior art keywords
benzodiazepin
tetrahydro
oxo
cgrp antagonists
salts
Prior art date
Application number
NO20073758A
Other languages
Norwegian (no)
Inventor
Henri Nico Doods
Klaus Rudolf
Stephan Georg Mueller
Dirk Stenkamp
Kirsten Arndt
Alexander Dreyer
Gerhard Schaenzle
Marco Santagostino
Fabio Paleari
Philipp Lustenberger
Original Assignee
Boehringer Ingelheim Int
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
Priority claimed from PCT/EP2005/003094 external-priority patent/WO2005092880A1/en
Application filed by Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of NO20073758L publication Critical patent/NO20073758L/en

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    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • AHUMAN NECESSITIES
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Dermatology (AREA)
  • Diabetes (AREA)
  • Endocrinology (AREA)
  • Cardiology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Addiction (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Communicable Diseases (AREA)
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Abstract

Det beskrives nye CGRP-antagonister med den generelle Formel (I) hvor B, R1 og R2 er som definert i krav 1, deres tautomerer, deres isomerer, deres diastereomerer, deres enantiomerer, deres hydrater, deres blandinger og deres salter, samt hydratene av saltene, særlig deres fysiologisk akseptable salter med uorganiske eller organiske syrer eller baser, medikamenter inneholdende disse forbindelsene, deres anvendelse og fremgangsmåte for deres fremstilling. ?? ?? ?? ?? 1New CGRP antagonists of general Formula (I) are disclosed wherein B, R1 and R2 are as defined in claim 1, their tautomers, their isomers, their diastereomers, their enantiomers, their hydrates, their mixtures and their salts, as well as the hydrates of the salts, especially their physiologically acceptable salts with inorganic or organic acids or bases, drugs containing these compounds, their use and process for their preparation. ?? ?? ?? ?? 1

NO20073758A 2005-03-23 2007-07-19 2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl-piperidines used as CGRP antagonists NO20073758L (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PCT/EP2005/003094 WO2005092880A1 (en) 2004-03-29 2005-03-23 Selected cgrp antagonists, methods for the production thereof and their use as medicaments
PCT/EP2006/002557 WO2006100026A1 (en) 2005-03-23 2006-03-21 2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl-piperidines used as cgrp antagonists

Publications (1)

Publication Number Publication Date
NO20073758L true NO20073758L (en) 2007-10-19

Family

ID=36406232

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20073758A NO20073758L (en) 2005-03-23 2007-07-19 2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl-piperidines used as CGRP antagonists

Country Status (19)

Country Link
EP (2) EP1992349B8 (en)
JP (1) JP4210322B2 (en)
KR (1) KR20070113317A (en)
CN (2) CN101146799A (en)
AU (1) AU2006226544A1 (en)
CA (1) CA2600189A1 (en)
DE (1) DE502006002066D1 (en)
DK (1) DK1863791T5 (en)
EA (1) EA012590B1 (en)
ES (1) ES2317512T3 (en)
HR (1) HRP20090011T3 (en)
MY (1) MY144635A (en)
NO (1) NO20073758L (en)
PL (1) PL1863791T3 (en)
PT (1) PT1863791E (en)
RS (1) RS50722B (en)
SI (1) SI1863791T1 (en)
WO (1) WO2006100026A1 (en)
ZA (1) ZA200705852B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10250082A1 (en) 2002-10-25 2004-05-13 Boehringer Ingelheim Pharma Gmbh & Co. Kg Selected CGRP antagonists, process for their preparation and their use as pharmaceuticals
DE102004015723A1 (en) * 2004-03-29 2005-10-20 Boehringer Ingelheim Pharma Selected CGRP antagonists, process for their preparation and their use as pharmaceuticals
US7696195B2 (en) 2004-04-22 2010-04-13 Boehringer Ingelheim International Gmbh Selected CGRP-antagonists, process for preparing them and their use as pharmaceutical compositions
EP1770086A1 (en) * 2005-09-29 2007-04-04 Boehringer Ingelheim Pharma GmbH & Co. KG Selected CGRP antagonists, process for their preparation as well as their use as medicaments
PE20080153A1 (en) * 2006-06-08 2008-04-14 Boehringer Ingelheim Int PHARMACEUTICAL COMPOSITION INCLUDING AN ANTAGONIST OF THE PEPTIDE RELATED TO THE CALCITONIN GENE (CGRP)

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10250082A1 (en) * 2002-10-25 2004-05-13 Boehringer Ingelheim Pharma Gmbh & Co. Kg Selected CGRP antagonists, process for their preparation and their use as pharmaceuticals
DE10250080A1 (en) * 2002-10-25 2004-05-13 Boehringer Ingelheim Pharma Gmbh & Co. Kg Selected CGRP antagonists, process for their preparation and their use as pharmaceuticals
EP1644332A1 (en) 2003-07-03 2006-04-12 Poseidon Pharmaceuticals A/S Diarylmethyl derivatives as potassium channel modulators
TW200533398A (en) 2004-03-29 2005-10-16 Bristol Myers Squibb Co Novel therapeutic agents for the treatment of migraine
EP1619187A1 (en) 2004-07-23 2006-01-25 Boehringer Ingelheim Pharma GmbH & Co. KG Process for the preparation of 3-(4-piperidinyl)- 2,3,4,5-tetrahydro-1,3-benzodiazepin-2(1H)-on

Also Published As

Publication number Publication date
AU2006226544A1 (en) 2006-09-28
CA2600189A1 (en) 2006-09-28
EP1992349B1 (en) 2013-07-31
EP1863791B1 (en) 2008-11-12
JP2008533083A (en) 2008-08-21
PL1863791T3 (en) 2009-04-30
EA200701843A1 (en) 2008-02-28
WO2006100026A8 (en) 2007-02-08
KR20070113317A (en) 2007-11-28
CN101146790A (en) 2008-03-19
WO2006100026A1 (en) 2006-09-28
RS50722B (en) 2010-08-31
PT1863791E (en) 2008-12-15
EP1992349B8 (en) 2013-10-09
JP4210322B2 (en) 2009-01-14
SI1863791T1 (en) 2009-04-30
ES2317512T3 (en) 2009-04-16
DK1863791T5 (en) 2010-10-04
DE502006002066D1 (en) 2008-12-24
EP1992349A1 (en) 2008-11-19
ZA200705852B (en) 2009-12-30
EP1863791A1 (en) 2007-12-12
CN101146799A (en) 2008-03-19
DK1863791T3 (en) 2009-02-16
EA012590B1 (en) 2009-10-30
HRP20090011T3 (en) 2009-02-28
MY144635A (en) 2011-10-14

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