PE20050444A1 - Compuestos de piridina como inhibidores de la peptidasa - Google Patents

Compuestos de piridina como inhibidores de la peptidasa

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Publication number
PE20050444A1
PE20050444A1 PE2004001030A PE2004001030A PE20050444A1 PE 20050444 A1 PE20050444 A1 PE 20050444A1 PE 2004001030 A PE2004001030 A PE 2004001030A PE 2004001030 A PE2004001030 A PE 2004001030A PE 20050444 A1 PE20050444 A1 PE 20050444A1
Authority
PE
Peru
Prior art keywords
methyl
aminomethyl
hydrocarbon group
pentilpyridine
methylphenyl
Prior art date
Application number
PE2004001030A
Other languages
English (en)
Inventor
Satoru Oi
Hironobu Maezaki
Nobuhiro Suzuki
Original Assignee
Takeda Pharmaceutical
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34557020&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20050444(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Takeda Pharmaceutical filed Critical Takeda Pharmaceutical
Publication of PE20050444A1 publication Critical patent/PE20050444A1/es

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    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D213/80Acids; Esters in position 3
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4406Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P3/04Anorexiants; Antiobesity agents
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    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
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Abstract

SE REFIERE A DERIVADOS DE PIRIDINA DONDE R1 Y R2 SON UN GRUPO HIDROCARBURO, OH; R3 ES UN GRUPO AROMATICO; R4 ES UN GRUPO AMINO OPCIONALMENTE SUSTITUIDO; L ES UN GRUPO DE HIDROCARBURO DE CADENA BIVALENTE; Q ES UN ENLACE O UN GRUPO HIDROCARBURO DE CADENA BIVALENTE; X ES UN ATOMO DE HIDROGENO, CIANO, NITRO, ACILO, HIDROXILO, TIOL CON LA CONDICION DE QUE X ES UN GRUPO ETOXICARBONILO ENTONCES Q ES UN GRUPO HIDROCARBURO DE CADENA BIVALENTE Y EL COMPUESTO NO ES 2,6-DIISOPROPIL-3-METILAMINOMETIL-4-(4-FLUORFENIL)-5-PENTILPIRIDINA, 2,6-DIISOPROPIL-3-AMINOMETIL-4-(4-FLUORFENIL)-5-PENTILPIRIDINA, 2,6-DIISOPROPIL-3-(ETILAMINO)METIL-4-(4-FLUORFENIL)-5-PENTILPIRIDINA, ENTRE OTROS. SON COMPUESTOS PREFERIDOS ACIDO 5-(AMINOMETIL)-2-METIL-4-(4-METILFENIL)-6-NEOPENTILNICOTINICO, ACIDO 5-(AMINOMETIL)-6-ISOBUTIL-2-METIL-4-(4-METILFENIL)NICOTINICO, 3-{[5-(AMINOMETIL)-6-ISOBUTIL-2-METIL-4-(4-METILFENIL)-PIRIDIN-3-IL]METOXI}-1-METIL-1H-PIRAZOL-4-CARBOXILATO, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO PARA LA PREPARACION. LOS COMPUESTOS MENCIONADOS SON INHIBIDORES DE LA PEPTIDASA Y SON UTILES PARA EL TRATMIENTO DE DIABETES
PE2004001030A 2003-10-31 2004-10-27 Compuestos de piridina como inhibidores de la peptidasa PE20050444A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2003373776 2003-10-31
JP2004030491 2004-02-06
JP2004165977 2004-06-03

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PE20050444A1 true PE20050444A1 (es) 2005-08-09

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US (1) US20070037807A1 (es)
EP (1) EP1678138A1 (es)
KR (2) KR20080067013A (es)
AR (1) AR046819A1 (es)
AU (1) AU2004285807A1 (es)
BR (1) BRPI0415960A (es)
CA (1) CA2543529A1 (es)
CO (1) CO5690607A2 (es)
IL (1) IL174608A0 (es)
MX (1) MXPA06003979A (es)
NO (1) NO20062516L (es)
NZ (1) NZ546787A (es)
PE (1) PE20050444A1 (es)
TW (1) TW200523252A (es)
WO (1) WO2005042488A1 (es)

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AR045047A1 (es) 2003-07-11 2005-10-12 Arena Pharm Inc Derivados arilo y heteroarilo trisustituidos como moduladores del metabolismo y de la profilaxis y tratamiento de desordenes relacionados con los mismos
EP1782832A4 (en) * 2004-08-26 2009-08-26 Takeda Pharmaceutical MEANS FOR THE TREATMENT OF DIABETES
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