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PE20040765A1 - 4-amino piperidinas n,n-disustituidas como inhibidores de la captacion de monoamina - Google Patents

4-amino piperidinas n,n-disustituidas como inhibidores de la captacion de monoamina

Info

Publication number
PE20040765A1
PE20040765A1 PE2003001225A PE2003001225A PE20040765A1 PE 20040765 A1 PE20040765 A1 PE 20040765A1 PE 2003001225 A PE2003001225 A PE 2003001225A PE 2003001225 A PE2003001225 A PE 2003001225A PE 20040765 A1 PE20040765 A1 PE 20040765A1
Authority
PE
Peru
Prior art keywords
alkyl
halogen
inhibitors
cyane
methylpropyl
Prior art date
Application number
PE2003001225A
Other languages
English (en)
Inventor
Manuel Javier Cases-Thomas
Barry Peter Clark
Peter Thaddeus Gallagher
Virginia Ann Wood
John Joseph Masters
Graham Henry Timms
Maria Ann Whatton
Jeremy Gilmore
Original Assignee
Lilly Co Eli
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 GB0228482A external-priority patent/GB0228482D0/en
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of PE20040765A1 publication Critical patent/PE20040765A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom 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
    • A61P25/00—Drugs for disorders of the nervous system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

SE REFIERE A COMPUESTOS DE FORMULA I, DONDE n ES 1, 2 O 3; R1 ES ALQUILO(C2-C10), ALQUENILO(C2-C10), CICLOALQUILO(C3-C8) O CICLOALQUIL(C4-C10)-ALQUILO, DONDE UN ENLACE C-C DEL CICLOALQUIL ESTA SUSTITUIDO POR UN ENLACE C-O, S-C o C=C, Y OPCIONALMENTE SUSTITUIDO POR 1 A 7 SUSTITUYENTES DE HALOGENO Y/O CON 1 A 3 HIDROXI, CIANO, ALQUILO(C1-C4), ENTRE OTROS; R2, R3 Y R4 SON H, ALQUILO(C1-C4), ALQUILO(C1-C4)-S(O)x DONDE x ES 0, 1 O 2, ALCOXI(C1-C4) (OPCIONALMENTE SUSTITUIDO CON 1 A 7 HALOGENOS), CIANO, HALOGENO, ENTRE OTROS; O R2 Y R3 O R3 Y R4, JUNTOS FORMAN UN ANILLO DE BENCENO ADICIONAL (OPCIONALMENTE SUSTITUIDO POR 1 A 3 HALOGENOS, ALQUILO(C1-C4) O ALCOXI(C1-C4); R5 Y R6 SON H, HALOGENO, ALQUILO(C1-C4), ALCOXI(C1-C4) (OPCIONALMENTE SUSTITUIDOS CON 1 A 7 HALOGENOS); R7 Y R8 SON H O ALQUILO(C1-C4); R9 Y R10 SON H, HALOGENO, HIDROXI, CIANO, ALQUILO C1-C4 O ALCOXI(C1-C4). SON COMPUESTOS PREFERIDOS: N-(1-METILETIL)-N-{[2-(TRIFLUOROMETIL)FENIL]METIL}PIPERIDIN-4-AMINA, N-(2-METILPROPIL)-N-{[4-(METOXI)FENIL]METIL}PIPERIDIN-4-AMINA, N-(2-METILPROPIL)-N-{[4-(CLORO)FENIL]METIL}PIPERIDIN-4-AMINA, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA SU PRODUCCION Y UNA FORMA FARMACEUTICA QUE LO CONTIENE. ESTOS COMPUESTOS SON INHIBIDORES DE LA CAPTACION DE SEROTONINA Y/O NOREPINEFRINA Y/O DOPAMINA Y SON UTILES PARA EL TRATAMIENTO DE TRANSTORNOS DEL SISTEMA NERVIOSO CENTRAL O PERIFERICO
PE2003001225A 2002-12-06 2003-12-02 4-amino piperidinas n,n-disustituidas como inhibidores de la captacion de monoamina PE20040765A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0228482A GB0228482D0 (en) 2002-12-06 2002-12-06 Inhibitors of monoamine uptake
US43472002P 2002-12-18 2002-12-18

Publications (1)

Publication Number Publication Date
PE20040765A1 true PE20040765A1 (es) 2004-12-02

Family

ID=32510397

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2003001225A PE20040765A1 (es) 2002-12-06 2003-12-02 4-amino piperidinas n,n-disustituidas como inhibidores de la captacion de monoamina

Country Status (6)

Country Link
US (1) US20060079554A1 (es)
EP (1) EP1569905A2 (es)
AR (1) AR042284A1 (es)
AU (1) AU2003290735A1 (es)
PE (1) PE20040765A1 (es)
WO (1) WO2004052858A2 (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE602004011221T2 (de) 2003-06-11 2009-01-02 Eli Lilly And Co., Indianapolis 3-amino-pyrrolidine als inhibitoren der monoamin-wiederaufnahme
WO2005053663A2 (en) * 2003-11-24 2005-06-16 Eli Lilly And Company Norepinephrine reuptake inhibitors useful for treatment of cognitive failure
CA2548304A1 (en) * 2003-12-12 2005-07-07 Eli Lilly And Company Selective norepinephrine reuptake inhibitors for the treatment of hot flashes, impulse control disorders and personality change due to a general medical condition
DE602005021871D1 (de) 2004-02-27 2010-07-29 Lilly Co Eli 4-aminopiperidinderivate als inhibitoren der monoamin-aufnahme
WO2005118531A1 (en) * 2004-06-01 2005-12-15 Eli Lilly And Company Aminomethyl-azacycle derivatives as inhibitors of monoamine uptake
NZ564759A (en) * 2005-06-30 2011-08-26 Prosidion Ltd GPCR agonists
JP2009513573A (ja) * 2005-09-30 2009-04-02 メルク エンド カムパニー インコーポレーテッド コレステリルエステル転送蛋白阻害剤
AU2007254232A1 (en) 2006-05-19 2007-11-29 Wyeth N-benzoyl-and N-benzylpyrrolidin-3-ylamines as histamine-3 antagonists
UA112897C2 (uk) 2012-05-09 2016-11-10 Байєр Фарма Акцієнгезелльшафт Біциклічно заміщені урацили та їх застосування для лікування і/або профілактики захворювань
US9751843B2 (en) 2013-11-08 2017-09-05 Bayer Pharma Aktiengesellschaft Substituted uracils and use thereof
EP3271337B1 (de) 2015-03-18 2021-03-03 pH Pharma Co., Ltd. Verfahren zur herstellung von (4s)-4-[4-cyano-2-(methylsulfonyl)phenyl]-3,6-dimethyl-2-oxo-1-[3-(trifluormethyl)phenyl]-1,2,3,4-tetrahydro pyrimidin-5-carbonitril
WO2018045376A2 (en) * 2016-09-02 2018-03-08 Ikaria Inc. Functionally modified polypeptides and radiobiosynthesis
CN110256285B (zh) * 2019-07-09 2022-03-18 上海出入境检验检疫局动植物与食品检验检疫技术中心 一种稳定同位素标记拟除虫菊酯的合成方法
WO2024105007A1 (en) * 2022-11-15 2024-05-23 Samsara Therapeutics Inc. Autophagy inducing compounds and uses thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3069716D1 (en) * 1979-10-01 1985-01-10 Sandoz Ag Dibenzazepine derivatives, their production and pharmaceutical compositions containing them
EP0255134B1 (en) * 1986-07-31 1993-03-03 Otsuka Pharmaceutical Co., Ltd. Carbostyril derivatives and salts thereof, process for preparing them, and cardiotonic composition containing same
US5567718A (en) * 1994-08-11 1996-10-22 Hoechst Marion Roussel Inc. 2,3-dihydro-1h-isoindole derivatives and their use as serotonin reuptake inhibitors
BR0314811A (pt) * 2002-10-04 2005-08-02 Ucb Sa Composto, uso do mesmo, e, intermediário de sìntese

Also Published As

Publication number Publication date
US20060079554A1 (en) 2006-04-13
WO2004052858A2 (en) 2004-06-24
WO2004052858A3 (en) 2004-08-12
AR042284A1 (es) 2005-06-15
AU2003290735A1 (en) 2004-06-30
AU2003290735A8 (en) 2004-06-30
EP1569905A2 (en) 2005-09-07

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