PE107498A1 - Compuestos opticamente activos - Google Patents

Compuestos opticamente activos

Info

Publication number
PE107498A1
PE107498A1 PE1997000741A PE00074197A PE107498A1 PE 107498 A1 PE107498 A1 PE 107498A1 PE 1997000741 A PE1997000741 A PE 1997000741A PE 00074197 A PE00074197 A PE 00074197A PE 107498 A1 PE107498 A1 PE 107498A1
Authority
PE
Peru
Prior art keywords
alkyl
ilo
indol
methyl
phenyl
Prior art date
Application number
PE1997000741A
Other languages
English (en)
Inventor
Marc Gerspacher
Sprecher Andreas Von
Stefan Stutz
Silvio Roggo
Robert Mah
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 PE107498A1 publication Critical patent/PE107498A1/es

Links

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)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

SE REFIEREN A COMPUESTOS DE FORMULA (I), EN DONDE: R ES FENILO OPCIONALMENTE SUSTITUIDO POR HASTA TRES SUSTITUYENTES HALOGENO, ALQUILO, CF3, OH o ALCOXI, DE PREFERENCIA ES 3,5-BISTRIFLUOROMETIL-FENILO; R1 ES H o ALQUILO, DE PREFERENCIA ES METILO; R2 ES H, ALQUILO o FENILO; R3 ES FENILO OPCIONALMENTE SUSTITUIDO, NAFTILO, 1H-INDOL-3-ILO o 1-ALQUILO-INDOL-3-ILO, DE PREFERENCIA ES 4-CLOROFENILO, 3,4-CLOROFENILO o 1-METIL-INDOL-3-ILO; R4` Y R4" SON H o ALQUILO, SIENDO AL MENOS UNO DE ELLOS HIDROGENO; R5 ES CICLOALQUILO C3-C8, D o L-AZACICLOHEPTAN-2-ON-3-ILO; UN COMPUESTO (I) PREFERIDO ES LA AMIDA N-[(R) o (S) -EPSILON-CAPROLACTAMA-3-ILICA] DEL ACIDO (4R)-[N'-METIL-N'-(3,5-BISTRIFLUOROMETIL-BENZOIL)-AMINO]-5-(1-METIL-INDOL-3-IL)-PENT-2-ENOICO. TAMBIEN SE REFIEREN A LOS PROCEDIMIENTOS DE PREPARACION DE (I), QUE COMPRENDEN: (A) N-ACILAR R1HN-CH(CHR2R3)-CR4'=CR4"-CO-NHR5 CON R-COOH; o (B) CONDENSAR R-CONR1-CH(CHR2R3)-CR4'=CR4"-COOH CON UN CICLOALQUILO C3-C8-AMINA o D(+) o L(-)-3-AMINO-EPSILON-CAPROLACTAMA; o (C) SINTETIZAR EL DOBLE ENLACE MEDIANTE UNA REACCION DE WITTIG O UNA VARIANTE DE LA MISMA POR EJEMPLO DE WITTIG-HORNER. LOS COMPUESTOS DE FORMULA (I) ACTUAN COMO ANTAGONISTAS DE NEUROQUININA NK1 Y NK2, SIENDO UTILES EN EL TRATAMIENTO DE LA HIPERTENSION, ASMA, BRONQUITIS CRONICA, COLITIS ULCERATIVA, ENFERMEDAD DE CROHN, ENTRE OTROS
PE1997000741A 1996-08-22 1997-08-20 Compuestos opticamente activos PE107498A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH206196 1996-08-22

Publications (1)

Publication Number Publication Date
PE107498A1 true PE107498A1 (es) 1999-01-28

Family

ID=4225003

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1997000741A PE107498A1 (es) 1996-08-22 1997-08-20 Compuestos opticamente activos

Country Status (32)

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

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
CN1874766A (zh) 2003-10-27 2006-12-06 诺瓦提斯公司 神经激肽拮抗剂在尿失禁治疗中的用途
EP1691814B9 (en) * 2003-12-01 2013-02-20 Cambridge Enterprise Limited Anti-inflammatory agents
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 (en) * 2006-12-22 2008-07-02 Novartis AG Pharmaceutical formulation comprising neurokinin antagonist
EP2117538A1 (en) 2007-01-24 2009-11-18 Glaxo Group Limited Pharmaceutical compositions comprising 2-methoxy-5- (5-trifluoromethyl-tetrazol-i-yl-benzyl) - (2s-phenyl-piperidin-3s-yl-)
UA105182C2 (ru) 2008-07-03 2014-04-25 Ньюрексон, Інк. Бензоксазины, бензотиазины и родственные соединения, которые имеют ингибирующую nos активность
US20120077803A1 (en) * 2009-02-24 2012-03-29 Novartis Ag Uses Of NK Receptor Antagonists
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
US5472978A (en) 1991-07-05 1995-12-05 Merck Sharp & Dohme Ltd. Aromatic compounds, pharmaceutical compositions containing them and their use in therapy
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 (de) * 1994-12-08 1996-06-12 Ciba-Geigy Ag Aromatisch substituierte Omega-Aminoalkansäureamide und Alkansäurediamide und ihre Verwendung als Renininhibitoren
CZ288345B6 (en) 1995-02-22 2001-05-16 Novartis Ag Arylacylaminoethanes, process of their preparation and pharmaceutical preparation in which they are comprised

Also Published As

Publication number Publication date
AR009266A1 (es) 2000-04-12
JP2001503387A (ja) 2001-03-13
CN1119328C (zh) 2003-08-27
ATE224875T1 (de) 2002-10-15
ZA977493B (en) 1998-08-03
EP0923550A1 (en) 1999-06-23
PL193731B1 (pl) 2007-03-30
AU4299397A (en) 1998-03-06
US6319917B1 (en) 2001-11-20
HK1021372A1 (en) 2000-06-09
NO990786L (no) 1999-03-25
SI0923550T1 (en) 2003-02-28
WO1998007694A1 (en) 1998-02-26
PL331740A1 (en) 1999-08-02
KR100467402B1 (ko) 2005-01-24
RU2185375C2 (ru) 2002-07-20
TR199900363T2 (xx) 1999-04-21
TW438777B (en) 2001-06-07
CZ58199A3 (cs) 1999-06-16
AU721850B2 (en) 2000-07-13
HUP0001165A3 (en) 2002-02-28
PT923550E (pt) 2003-01-31
EP0923550B1 (en) 2002-09-25
NO990786D0 (no) 1999-02-19
DE69715886D1 (de) 2002-10-31
CA2264065A1 (en) 1998-02-26
ES2184083T3 (es) 2003-04-01
ID18059A (id) 1998-02-26
SK22199A3 (en) 2000-02-14
CN1233238A (zh) 1999-10-27
HU226395B1 (en) 2008-11-28
IL128631A0 (en) 2000-01-31
DE69715886T2 (de) 2003-05-15
NZ334736A (en) 2000-09-29
DK0923550T3 (da) 2003-01-06
HUP0001165A2 (hu) 2000-11-28
NO312292B1 (no) 2002-04-22
CO4900047A1 (es) 2000-03-27
IL128631A (en) 2002-09-12
MY132550A (en) 2007-10-31
BR9711350A (pt) 1999-08-17
JP3654908B2 (ja) 2005-06-02
KR20000068325A (ko) 2000-11-25
CA2264065C (en) 2008-02-05
CZ294233B6 (cs) 2004-11-10
SK283991B6 (sk) 2004-07-07

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Legal Events

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FG Grant, registration
FD Application declared void or lapsed