PE20090103A1 - DERIVADOS DE PIRIDINA Y PIRIMIDINA COMO ANTAGONISTAS DEL mGluR2 - Google Patents

DERIVADOS DE PIRIDINA Y PIRIMIDINA COMO ANTAGONISTAS DEL mGluR2

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Publication number
PE20090103A1
PE20090103A1 PE2008000591A PE2008000591A PE20090103A1 PE 20090103 A1 PE20090103 A1 PE 20090103A1 PE 2008000591 A PE2008000591 A PE 2008000591A PE 2008000591 A PE2008000591 A PE 2008000591A PE 20090103 A1 PE20090103 A1 PE 20090103A1
Authority
PE
Peru
Prior art keywords
alkyl
trifluoromethyl
antagonists
mglur2
pyridine
Prior art date
Application number
PE2008000591A
Other languages
English (en)
Inventor
Silvia Gatti Mcarthur
Juergen Wichmann
Thomas Woltering
Original Assignee
Hoffmann La Roche
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=39457413&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20090103(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20090103A1 publication Critical patent/PE20090103A1/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms 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
    • A61K31/435Heterocyclic 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
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • A61P21/02Muscle relaxants, e.g. for tetanus or cramps
    • 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
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
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    • AHUMAN NECESSITIES
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    • AHUMAN NECESSITIES
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • C07ORGANIC CHEMISTRY
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • 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
    • C07D401/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Addiction (AREA)
  • Psychology (AREA)
  • Hospice & Palliative Care (AREA)
  • Endocrinology (AREA)
  • Diabetes (AREA)
  • Ophthalmology & Optometry (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Hematology (AREA)
  • Anesthesiology (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Reproductive Health (AREA)
  • Emergency Medicine (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Otolaryngology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pyridine Compounds (AREA)

Abstract

SE REFIERE A COMPUESTOS DE FORMULA I, EN EL QUE UNO DE ENTRE X O Y ES N Y EL OTRO ES CH, O AMBOS X E Y SON N; Q ES S, O, -CH=N- O -N=CH-; A ES ARILO O UN HETEROARILO DE 5 A 6 MIEMBROS; B ES ARILO O UN HETEROARILO DE 5 A 6 MIEMBROS, OPCIONALMENTE SUSTITUIDOS POR HALO, ALQUILO(C1-C6), -(SO2)-OH, NRaRb, ENTRE OTROS; DONDE Ra Y Rb SON H, ALQUILO(C1-C6) O -(CO)-ALQUILO(C1-C6); R1 ES H, HALOGENO O ALQUILO(C1-C6); R2 ES CIANO, ALCOXI(C1-C6), HALOALQUILO(C1-C6), NRjRk, ENTRE OTROS; DONDE Rj Y Rk SON H, ARILO, CICLOALQUILO(C3-C8), ENTRE OTROS. SON SELECCIONADOS 5-{3-[4-(5-CLORO-TIOFEN-2-IL)-6-TRIFLUOROMETIL-PIRIMIDIN-2-IL]-FENIL}-PIRIDIN-2-ILAMINA, 4-[4-TRIFLUOROMETIL-6-(6-TRIFLUOROMETIL-PIRIDIN-3-IL)-PIRIMIDIN-2-IL]-[2,3']BIPIRIDINIL-6'-ILAMINA, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCESO DE PREPARACION Y COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DEL RECEPTOR DE GLUTAMATO METABOTROPICO, UTILES EN LA PREVENCION Y/O TRATAMIENTO DE TRASTORNOS DEL SNC, TALES COMO PSICOSIS, ALZHEIMER, PERDIDA DE MEMORIA, GLIOMA, ENTRE OTROS
PE2008000591A 2007-04-02 2008-04-01 DERIVADOS DE PIRIDINA Y PIRIMIDINA COMO ANTAGONISTAS DEL mGluR2 PE20090103A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP07105429 2007-04-02

Publications (1)

Publication Number Publication Date
PE20090103A1 true PE20090103A1 (es) 2009-02-13

Family

ID=39457413

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2008000591A PE20090103A1 (es) 2007-04-02 2008-04-01 DERIVADOS DE PIRIDINA Y PIRIMIDINA COMO ANTAGONISTAS DEL mGluR2

Country Status (17)

Country Link
US (2) US8012986B2 (es)
EP (1) EP2142527B1 (es)
JP (1) JP5303544B2 (es)
KR (1) KR101143152B1 (es)
CN (1) CN101641346B (es)
AR (1) AR065891A1 (es)
AT (1) ATE493400T1 (es)
AU (1) AU2008233956B2 (es)
BR (1) BRPI0809971A2 (es)
CA (1) CA2681733A1 (es)
CL (1) CL2008000936A1 (es)
DE (1) DE602008004236D1 (es)
IL (1) IL200780A (es)
MX (1) MX2009010505A (es)
PE (1) PE20090103A1 (es)
TW (1) TW200845999A (es)
WO (1) WO2008119689A1 (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2009203693B2 (en) * 2008-01-11 2012-06-07 Novartis Ag Pyrimidines as kinase inhibitors
EP2604602A4 (en) 2010-08-11 2013-12-18 Taisho Pharmaceutical Co Ltd HETEROARYLPYRAZOLDERIVAT
JP2014062047A (ja) * 2011-01-21 2014-04-10 Taisho Pharmaceutical Co Ltd ピラゾール誘導体
AU2012311458B2 (en) * 2011-09-21 2016-02-04 Cellzome Limited Morpholino substituted urea or carbamate derivatives as mTOR inhibitors
CA2864085C (en) * 2012-02-08 2021-11-23 Sunovion Pharmaceuticals Inc. Heteroaryl compounds and methods of use thereof
JP2015534993A (ja) 2012-10-23 2015-12-07 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffma 自閉症性障害の処置のためのmGlu2/3アンタゴニスト
WO2015162076A2 (en) 2014-04-23 2015-10-29 F. Hoffmann-La Roche Ag Mglu2/3 antagonists for the treatment of intellectual disabilities
US9969726B2 (en) * 2014-06-10 2018-05-15 Sanford-Burnham Medical Research Institute Metabotropic glutamate receptor negative allosteric modulators (NAMS) and uses thereof
MA45857A (fr) 2016-07-29 2021-05-19 Sunovion Pharmaceuticals Inc Composés et compositions, et utilisations associées
JP2019523279A (ja) 2016-07-29 2019-08-22 サノビオン ファーマシューティカルズ インクSunovion Pharmaceuticals Inc. 化合物および組成物ならびにそれらの使用
CA3070993A1 (en) 2017-08-02 2019-02-07 Sunovion Pharmaceuticals Inc. Isochroman compounds and uses thereof
US20210269414A1 (en) * 2018-06-22 2021-09-02 Bayer Aktiengesellschaft Process for preparing tricyclic compounds
JP2022525169A (ja) 2019-03-14 2022-05-11 サノビオン ファーマシューティカルズ インク イソクロマニル化合物の塩およびその結晶体、ならびにそれらの製造方法、治療用途および医薬組成物

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA74419C2 (uk) * 2001-02-21 2005-12-15 Ен Пі Ес Фармасьютікалс, Інк. Заміщені піридини та їх застосування як антагоністів рецептору метаботропного глутамату
JP2006522164A (ja) * 2003-04-03 2006-09-28 メルク エンド カムパニー インコーポレーテッド 代謝調節型グルタミン酸受容体−5のジアリール置換ピラゾール修飾因子
WO2004089308A2 (en) 2003-04-04 2004-10-21 Merck & Co., Inc. Di-aryl substituted pyrrole modulators of metabotropic glutamate receptor-5
JP4110173B2 (ja) * 2003-11-04 2008-07-02 高砂香料工業株式会社 白金錯体及び発光素子
US20060173048A1 (en) 2005-02-03 2006-08-03 Mcarthur Silvia G Imidazole derivatives
RU2451673C2 (ru) 2006-03-29 2012-05-27 Ф. Хоффманн-Ля Рош Аг ПРОИЗВОДНЫЕ ПИРИДИНА И ПИРИМИДИНА В КАЧЕСТВЕ АНТАГОНИСТОВ mGluR2
US20070236568A1 (en) 2006-04-11 2007-10-11 Metke Anthony R Method and system for communicating incident scene information

Also Published As

Publication number Publication date
JP2010524852A (ja) 2010-07-22
KR20090117902A (ko) 2009-11-13
DE602008004236D1 (de) 2011-02-10
IL200780A0 (en) 2010-05-17
JP5303544B2 (ja) 2013-10-02
EP2142527A1 (en) 2010-01-13
US8012986B2 (en) 2011-09-06
EP2142527B1 (en) 2010-12-29
CN101641346B (zh) 2013-11-06
ATE493400T1 (de) 2011-01-15
BRPI0809971A2 (pt) 2014-10-07
CA2681733A1 (en) 2008-10-09
US8415380B2 (en) 2013-04-09
MX2009010505A (es) 2009-10-19
US20110263615A1 (en) 2011-10-27
IL200780A (en) 2013-01-31
TW200845999A (en) 2008-12-01
AR065891A1 (es) 2009-07-08
CL2008000936A1 (es) 2008-10-03
KR101143152B1 (ko) 2012-05-08
WO2008119689A1 (en) 2008-10-09
AU2008233956A1 (en) 2008-10-09
CN101641346A (zh) 2010-02-03
AU2008233956B2 (en) 2013-05-02
US20080280924A1 (en) 2008-11-13

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