SK283991B6 - Acylaminoalkenylénamidové deriváty ako NK1 a NK2 antagonisty, spôsob ich prípravy, farmaceutický prostriedok s ich obsahom a ich použitie - Google Patents

Acylaminoalkenylénamidové deriváty ako NK1 a NK2 antagonisty, spôsob ich prípravy, farmaceutický prostriedok s ich obsahom a ich použitie Download PDF

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Publication number
SK283991B6
SK283991B6 SK221-99A SK22199A SK283991B6 SK 283991 B6 SK283991 B6 SK 283991B6 SK 22199 A SK22199 A SK 22199A SK 283991 B6 SK283991 B6 SK 283991B6
Authority
SK
Slovakia
Prior art keywords
methyl
group
compound
formula
lower alkyl
Prior art date
Application number
SK221-99A
Other languages
English (en)
Slovak (sk)
Other versions
SK22199A3 (en
Inventor
Marc Gerspacher
Sprecher Andreas Von
Robert Mah
Silvio Roggo
Stefan Stutz
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of SK22199A3 publication Critical patent/SK22199A3/sk
Publication of SK283991B6 publication Critical patent/SK283991B6/sk

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/12—Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D209/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with an alkyl or cycloalkyl radical attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings 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
    • C07D223/12—Nitrogen atoms not forming part of a nitro radical

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (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)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Pain & Pain Management (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Cardiology (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
SK221-99A 1996-08-22 1997-08-13 Acylaminoalkenylénamidové deriváty ako NK1 a NK2 antagonisty, spôsob ich prípravy, farmaceutický prostriedok s ich obsahom a ich použitie SK283991B6 (sk)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH206196 1996-08-22
PCT/EP1997/004436 WO1998007694A1 (fr) 1996-08-22 1997-08-13 Derives d'acylaminoalkenylene comme antagonistes de nk1 et nk2

Publications (2)

Publication Number Publication Date
SK22199A3 SK22199A3 (en) 2000-02-14
SK283991B6 true SK283991B6 (sk) 2004-07-07

Family

ID=4225003

Family Applications (1)

Application Number Title Priority Date Filing Date
SK221-99A SK283991B6 (sk) 1996-08-22 1997-08-13 Acylaminoalkenylénamidové deriváty ako NK1 a NK2 antagonisty, spôsob ich prípravy, farmaceutický prostriedok s ich obsahom a ich použitie

Country Status (32)

Country Link
US (1) US6319917B1 (fr)
EP (1) EP0923550B1 (fr)
JP (1) JP3654908B2 (fr)
KR (1) KR100467402B1 (fr)
CN (1) CN1119328C (fr)
AR (1) AR009266A1 (fr)
AT (1) ATE224875T1 (fr)
AU (1) AU721850B2 (fr)
BR (1) BR9711350A (fr)
CA (1) CA2264065C (fr)
CO (1) CO4900047A1 (fr)
CZ (1) CZ294233B6 (fr)
DE (1) DE69715886T2 (fr)
DK (1) DK0923550T3 (fr)
ES (1) ES2184083T3 (fr)
HK (1) HK1021372A1 (fr)
HU (1) HU226395B1 (fr)
ID (1) ID18059A (fr)
IL (1) IL128631A (fr)
MY (1) MY132550A (fr)
NO (1) NO312292B1 (fr)
NZ (1) NZ334736A (fr)
PE (1) PE107498A1 (fr)
PL (1) PL193731B1 (fr)
PT (1) PT923550E (fr)
RU (1) RU2185375C2 (fr)
SI (1) SI0923550T1 (fr)
SK (1) SK283991B6 (fr)
TR (1) TR199900363T2 (fr)
TW (1) TW438777B (fr)
WO (1) WO1998007694A1 (fr)
ZA (1) ZA977493B (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6281300B1 (en) * 1998-03-20 2001-08-28 Exxon Chemical Patents, Inc. Continuous slurry polymerization volatile removal
GB0010958D0 (en) * 2000-05-05 2000-06-28 Novartis Ag Organic compounds
GB0203061D0 (en) * 2002-02-08 2002-03-27 Novartis Ag Organic compounds
GB2394417A (en) * 2002-10-24 2004-04-28 Novartis Ag Solid dispersion comprising a piperidine substance P antagonist and a carrier
GB0224788D0 (en) * 2002-10-24 2002-12-04 Novartis Ag Organic compounds
EP2158910A1 (fr) 2003-10-27 2010-03-03 Novartis Ag Utilisation d'antagonistes de neurokinine dans le traitement de l'incontinence urinaire
SI1691814T1 (sl) * 2003-12-01 2012-11-30 Cambridge Entpr Ltd Protivnetna zdravila
GB0402679D0 (en) * 2004-02-06 2004-03-10 Novartis Ag Organic compounds
JO2630B1 (en) 2006-04-13 2012-06-17 نوفارتيس ايه جي Organic compounds
GB0607532D0 (en) * 2006-04-13 2006-05-24 Novartis Ag Organic compounds
EP1938804A1 (fr) * 2006-12-22 2008-07-02 Novartis AG Préparation pharmaceutique comprenant un antagoniste de neurokinine
WO2008090114A1 (fr) 2007-01-24 2008-07-31 Glaxo Group Limited Compositions pharmaceutiques contenant du 2-méthoxy-5- (5-trifluorométhyl-tétrazol-i-yl-benzyl) - (2s-phényl-pipéridin-3s-yl-)
UA105182C2 (ru) 2008-07-03 2014-04-25 Ньюрексон, Інк. Бензоксазины, бензотиазины и родственные соединения, которые имеют ингибирующую nos активность
JP5425229B2 (ja) * 2009-02-24 2014-02-26 ノバルティス アーゲー Ｎｋ受容体アンタゴニストの使用
RU2697414C1 (ru) * 2018-05-11 2019-08-14 Общество с ограниченной ответственностью "АЙ БИ ДИ Терапевтикс" Новый антагонист тахикининовых рецепторов и его применение

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2110514A1 (fr) 1991-07-05 1993-01-21 Raymond Baker Composes aromatiques, compositions pharmaceutiques contenant lesdits composes et leur utilisation a des fins therapeutiques
MY110227A (en) * 1991-08-12 1998-03-31 Ciba Geigy Ag 1-acylpiperindine compounds.
US5217996A (en) 1992-01-22 1993-06-08 Ciba-Geigy Corporation Biaryl substituted 4-amino-butyric acid amides
EP0716077A1 (fr) * 1994-12-08 1996-06-12 Ciba-Geigy Ag Amides d'acides oméga-amino alcanoiques et diamides alcanoiques ayant un substituant aromatique et leur application en tant qu'inhibiteurs de leur rénine
DE69602087T2 (de) 1995-02-22 1999-09-09 Novartis Ag 1-aryl-2-acylamino-ethan-verbindungen und ihre verwendung als neurokinin- insbesondere als neurokinin-1-antagonisten

Also Published As

Publication number Publication date
EP0923550A1 (fr) 1999-06-23
ID18059A (id) 1998-02-26
NO312292B1 (no) 2002-04-22
KR100467402B1 (ko) 2005-01-24
IL128631A0 (en) 2000-01-31
AU4299397A (en) 1998-03-06
AR009266A1 (es) 2000-04-12
AU721850B2 (en) 2000-07-13
US6319917B1 (en) 2001-11-20
EP0923550B1 (fr) 2002-09-25
JP2001503387A (ja) 2001-03-13
JP3654908B2 (ja) 2005-06-02
IL128631A (en) 2002-09-12
CZ58199A3 (cs) 1999-06-16
SK22199A3 (en) 2000-02-14
CZ294233B6 (cs) 2004-11-10
DE69715886D1 (de) 2002-10-31
WO1998007694A1 (fr) 1998-02-26
CN1233238A (zh) 1999-10-27
CN1119328C (zh) 2003-08-27
NZ334736A (en) 2000-09-29
ES2184083T3 (es) 2003-04-01
DK0923550T3 (da) 2003-01-06
HU226395B1 (en) 2008-11-28
PE107498A1 (es) 1999-01-28
KR20000068325A (ko) 2000-11-25
CA2264065A1 (fr) 1998-02-26
NO990786L (no) 1999-03-25
PT923550E (pt) 2003-01-31
MY132550A (en) 2007-10-31
SI0923550T1 (en) 2003-02-28
PL331740A1 (en) 1999-08-02
BR9711350A (pt) 1999-08-17
CA2264065C (fr) 2008-02-05
HK1021372A1 (en) 2000-06-09
TW438777B (en) 2001-06-07
NO990786D0 (no) 1999-02-19
ATE224875T1 (de) 2002-10-15
HUP0001165A3 (en) 2002-02-28
CO4900047A1 (es) 2000-03-27
DE69715886T2 (de) 2003-05-15
ZA977493B (en) 1998-08-03
RU2185375C2 (ru) 2002-07-20
TR199900363T2 (xx) 1999-04-21
HUP0001165A2 (hu) 2000-11-28
PL193731B1 (pl) 2007-03-30

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Legal Events

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MM4A Patent lapsed due to non-payment of maintenance fees

Effective date: 20120813