ES2329553T3 - Pirroloquinolinas y piridoquinolinas sustituidas como agonistas y antagonistas de serotonina. - Google Patents

Pirroloquinolinas y piridoquinolinas sustituidas como agonistas y antagonistas de serotonina. Download PDF

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Publication number
ES2329553T3
ES2329553T3 ES01994318T ES01994318T ES2329553T3 ES 2329553 T3 ES2329553 T3 ES 2329553T3 ES 01994318 T ES01994318 T ES 01994318T ES 01994318 T ES01994318 T ES 01994318T ES 2329553 T3 ES2329553 T3 ES 2329553T3
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alkyl
substituted
case
independently selected
alkenyl
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ES2329553T4 (es
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John M. Fevig
Ian S. Mitchell
Taekyu Lee
Wenting Chen
Joseph Cacciola
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Bristol Myers Squibb Co
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Bristol Myers Squibb Co
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/16Peri-condensed 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
    • A61P1/14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • 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
    • 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
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/16Peri-condensed systems

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Child & Adolescent Psychology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Anesthesiology (AREA)
  • Nutrition Science (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Un compuesto de la fórmula (I): **(Ver fórmula)** o un estereoisómero o una forma de sal farmacéuticamente aceptable del mismo, en el que: b es un enlace sencillo, donde los hidrógenos puente son cis o trans; X es -CH2-, R1 se selecciona entre H, alquilo C1-5, alquenilo C2-5, alquinilo C2-5, cicloalquilo C3-6, -(alquil C1-3) cicloalquilo C3-6, -(alquenil C2-3)cicloalquilo C3-6 y -(alquinil C2-3)cicloalquilo C3-6, R6a es H o alquilo C1-4; R6b es H; como alternativa, R6a y R6b se toman juntos para formar =O o =S; R7 y R9, en cada caso, se seleccionan independientemente entre H, halo, -CF3, -OCF3, -OH, -CN, -NO2, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, alcoxi C1-4 y (haloalquil C1-4)oxi; R8 se selecciona entre H; fenilo sustituido con O-S R33; y -NR12R13; R12, en cada caso, se selecciona independientemente entre alquilo C1-4 sustituido con 0-1 R12a, alquenilo C2-4 sustituido con 0-1 R12a, alquinilo C2-4 sustituido con 0-1 R12a, cicloalquilo C3-6 sustituido con 0-3 R33, arilo sustituido con 0-5 R33; resto carbocíclico C3-10 sustituido con 0-3 R33 y sistema de anillos heterocíclicos de 5-10 miembros que contiene 1-4 heteroátomos seleccionados entre el grupo constituido por N, O y S sustituido con 0-3 R31; R12a, en cada caso, se selecciona independientemente entre fenilo sustituido con 0-5 R33; resto carbocíclico C3-10 sustituido con 0-3 R33 y sistema de anillos heterocíclicos de 5-10 miembros que contiene de 1-4 heteroátomos seleccionados entre el grupo constituido por N, O y S sustituido con 0-3 R31; R13, en cada caso, se selecciona independientemente entre H, alquilo C1-4, alquenilo C2-4 y alquinilo C2-4; como alternativa, R12 y R13, cuando se unen a N, pueden combinarse para formar un anillo heterocíclico bicíclico de 9 ó 10 miembros que contiene 1-3 heteroátomos seleccionados entre el grupo constituido por N, O y S, donde dicho sistema de anillos heterocíclicos bicíclico está insaturado o parcialmente saturado, donde dicho sistema de anillos heterocíclicos bicíclico está sustituido con 0-3 R16; R16, en cada caso, se selecciona independientemente entre H, OH, halo, CN, NO2, CF3, SO2R45, NR46R47, -C(=O) H, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, (haloalquil C1-3)-oxi-, (alquiloxi C1-3)-, y =O; R31, en cada caso, se selecciona independientemente entre H, OH, halo, CF3, SO2R45, NR46R47, alquilo C1-4 y =O; R33, en cada caso, se selecciona independientemente entre H, OH, halo, CN, NO2, CF3, SO2R 45, NR46R47, -C(=O)H, =O, fenilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, haloalquilo C1-4, (haloalquil C1-4)-oxi-, (alquiloxi C1-4)-, (alquiltio C1-4)-, (alquil C1-4)-C(=O)-, (alquil C1-4)-C(=O)NH-, (alquil C1-4)-OC(=O)-, (alquil C1-4)-C(=O)O-, (cicloalquil C3-6)-oxi-, (cicloalquilmetil C3-6)-oxi-; alquilo C1-6 sustituido con OH, metoxi, etoxi, propoxi, butoxi, -SO2R45, -NR46R47, NR46R47C(=O)- o (alquil C1-4)CO2-; y alquenilo C2-6 sustituido con OH, metoxi, etoxi, propoxi, butoxi, -SO2R45, -NR46R47, NR46R47C(=O)-, o (alquil C1-4)CO2-; R45 es alquilo C1-4; R46, en cada caso, se selecciona independientemente entre H y alquilo C1-4; R47, en cada caso, se selecciona independientemente entre H, alquilo C1-4, -C(=O)NH(alquilo C1-4), -SO2(alquilo C1-4), -C(=O)O(alquilo C1-4), -C(=O)( alquilo C1-4) y -C(=O)H; n es 1 ó 2; m es 1 ó 2; y n más m es 2, 3 ó 4.
ES01994318T 2000-12-20 2001-12-19 Pirroloquinolinas y piridoquinolinas sustituidas como agonistas y antagonistas de serotonina. Expired - Lifetime ES2329553T4 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US25674500P 2000-12-20 2000-12-20
US256745P 2000-12-20

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ES2329553T3 true ES2329553T3 (es) 2009-11-27
ES2329553T4 ES2329553T4 (es) 2010-12-07

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ES01994318T Expired - Lifetime ES2329553T4 (es) 2000-12-20 2001-12-19 Pirroloquinolinas y piridoquinolinas sustituidas como agonistas y antagonistas de serotonina.

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Country Link
US (1) US6777406B2 (es)
EP (1) EP1399445B9 (es)
JP (1) JP4386639B2 (es)
KR (1) KR20030070590A (es)
AT (1) ATE438646T1 (es)
AU (1) AU2002246726B2 (es)
BG (1) BG107863A (es)
BR (1) BR0116348A (es)
CA (1) CA2432181C (es)
CZ (1) CZ20031707A3 (es)
DE (1) DE60139511D1 (es)
EE (1) EE200300303A (es)
ES (1) ES2329553T4 (es)
HU (1) HUP0303530A3 (es)
IL (1) IL156261A0 (es)
IS (1) IS6851A (es)
MX (1) MXPA03005355A (es)
NO (1) NO20032798L (es)
PL (1) PL366627A1 (es)
RU (1) RU2003121306A (es)
SK (1) SK7032003A3 (es)
WO (1) WO2002059124A2 (es)
ZA (1) ZA200304304B (es)

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR031200A1 (es) 2000-11-03 2003-09-10 Wyeth Corp Cicloocta [b] [1,4] diazepino [6,7,1-hi] indoles y derivados
US6858604B2 (en) 2000-11-03 2005-02-22 Wyeth Cyclohepta[b][1,4]diazepino[6,7,1-hi]indoles and derivatives
AR031202A1 (es) 2000-11-03 2003-09-10 Wyeth Corp Ciclopenta(b) (1,4)diazepino(6,7,1-hi) indoles y derivados
TW200307540A (en) 2002-04-25 2003-12-16 Wyeth Corp [1, 4]Diazocino[7, 8, 1-hi] indole derivatives as antipsychotic and antiobesity agents
TWI312781B (en) 2002-04-25 2009-08-01 [1,4]diazepino[6,7,1-ij]quinoline derivatives as antipsychotic and antiobesity agents
TW200307682A (en) 2002-04-25 2003-12-16 Wyeth Corp 1,2,3,4,7,8-Hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline derivatives as antipsychotic and antiobesity agents
CL2004000826A1 (es) 2003-04-25 2005-03-04 Pfizer Uso de un agonista para el receptor 5-ht2c para preparar un medicamento util en el tratamiento de la incontinencia urinaria provocada por estres, con la condicion de que el agonista no sea 1-[6-cloro-5-(trifluorometil)-2-piridinil]piperazina (org-129
EP2248524A3 (en) 2004-08-25 2011-03-09 Takeda Pharmaceutical Company Limited Preventives/remedies for stress urinary incontinence and method of screening the same
US20070021612A1 (en) * 2004-11-04 2007-01-25 University Of Notre Dame Du Lac Processes and compounds for preparing histone deacetylase inhibitors and intermediates thereof
US7235688B1 (en) 2004-11-04 2007-06-26 University Of Notre Dame Du Lac Process for preparing histone deacetylase inhibitors and intermediates thereof
GT200500317A (es) * 2004-11-05 2006-10-27 Proceso para preparar compuestos de quinolina y productos obtenidos de los mismos
AR054849A1 (es) * 2005-07-26 2007-07-18 Wyeth Corp Diazepinoquinolinas, sintesis de las mismas, e intermediarios para obtenerlas
TW200734334A (en) * 2006-01-13 2007-09-16 Wyeth Corp Treatment of substance abuse
JP2009531434A (ja) * 2006-03-24 2009-09-03 ワイス 痛みの治療
CN101410112A (zh) * 2006-03-24 2009-04-15 惠氏公司 治疗抑郁症的新治疗组合
EP2742936A1 (en) 2006-05-16 2014-06-18 Takeda Pharmaceutical Company Limited Fused heterocyclic compound and use thereof
CL2008002777A1 (es) * 2007-09-21 2010-01-22 Wyeth Corp Metodo de preparacion de compuestos diazepinoquinolinicos quirales por recristalizacion en un sistema de solvente ternario.
US20100266504A1 (en) 2007-11-15 2010-10-21 Takahiro Matsumoto Condensed pyridine derivative and use thereof
AU2010303270A1 (en) 2009-10-09 2012-05-03 Zafgen Corporation Sulphone compounds for use in the treatment of obesity
EP2510949A4 (en) 2009-12-11 2013-11-13 Astellas Pharma Inc THERAPEUTICS FOR FIBROMYALGIA
BR112013001613A2 (pt) * 2010-07-22 2016-05-24 Zafgen Inc compostos tricíclicos e métodos para fazer e usar os mesmos.
US9321740B2 (en) 2011-01-26 2016-04-26 Zafgen, Inc. Tetrazole compounds and methods of making and using same
BR112013028665A2 (pt) 2011-05-06 2016-09-06 Zafgen Inc compostos de sulfonamida tricíclicos e métodos para fazer e usar os mesmos
MX343688B (es) 2011-05-06 2016-11-16 Zafgen Inc Compuestos tricíclicos de sulfonamida y pirazolo y métodos para su fabricación y uso.
KR101979039B1 (ko) 2011-05-06 2019-05-15 자프겐 인크. 부분 포화된 삼환식 화합물 및 그리고 그의 제조방법 및 그를 이용하는 방법
US9440943B2 (en) 2012-01-18 2016-09-13 Zafgen, Inc. Tricyclic sulfone compounds and methods of making and using same
JP6035347B2 (ja) 2012-01-18 2016-11-30 ザフゲン,インコーポレイテッド 三環式スルホンアミド化合物ならびにその作製および使用方法
KR20150080614A (ko) 2012-11-05 2015-07-09 자프겐 인크. 비만의 치료 및/또는 제어에서 사용하기 위한 트리시클릭 화합물
NZ707773A (en) 2012-11-05 2019-05-31 Zafgen Inc Methods of treating liver diseases
MX2015005732A (es) 2012-11-05 2015-12-16 Zafgen Inc Compuestos tricíclicos y métodos para hacer y utilizar los mismos.
EP2919788A4 (en) 2012-11-14 2016-05-25 Univ Johns Hopkins METHODS AND COMPOSITIONS FOR THE TREATMENT OF SCHIZOPHRENIA
EP2981266B1 (en) * 2013-03-04 2018-01-03 Daya CNS LLC Pentacyclic pyridoindolobenz[b,d]azepine derivatives and uses thereof
WO2015066344A1 (en) 2013-11-01 2015-05-07 Arena Pharmaceuticals, Inc. 5-ht2c receptor agonists and compositions and methods of use
EP3733204A4 (en) 2017-12-27 2021-09-15 Takeda Pharmaceutical Company Limited THERAPEUTIC FOR EXERCISE INCONTINENCE AND STAIR INCONTINENCE
CN109897039B (zh) * 2019-03-13 2021-03-30 中国科学院化学研究所 一种制备吡咯并[3,2,1-ij]喹啉酮化合物的方法
US20240208973A1 (en) * 2021-04-13 2024-06-27 The Regents Of The University Of California Tetracyclic compounds for treating brain disorders

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4013652A (en) 1972-06-19 1977-03-22 Endo Laboratories, Inc. Pyridopyrrolobenzoxazine
US4238607A (en) 1972-06-19 1980-12-09 Endo Laboratories Inc. Pyridopyrrolo benzheterocycles
US3914421A (en) 1972-06-19 1975-10-21 Endo Lab Pyridopyrrolobenzheterocycles for combatting depression
US4115577A (en) 1972-06-19 1978-09-19 Endo Laboratories, Inc. Pyridopyrrolobenzheterocycles
US4183936A (en) 1972-06-19 1980-01-15 Endo Laboratories, Inc. Pyridopyrrolobenzheterocycles
US4219550A (en) 1978-11-09 1980-08-26 E. I. Du Pont De Nemours And Company Cis- and trans- octahydropyridopyrrolobenzheterocycles
HUT61548A (en) * 1990-08-27 1993-01-28 Sandoz Ag Process for producing indolonaphthyridine derivatives and pharmaceutical compositions comprising such compounds

Also Published As

Publication number Publication date
US20040092502A1 (en) 2004-05-13
KR20030070590A (ko) 2003-08-30
CA2432181C (en) 2009-11-17
JP4386639B2 (ja) 2009-12-16
EP1399445B1 (en) 2009-08-05
HUP0303530A3 (en) 2012-10-29
NO20032798D0 (no) 2003-06-19
MXPA03005355A (es) 2004-05-27
IL156261A0 (en) 2004-01-04
ES2329553T4 (es) 2010-12-07
CA2432181A1 (en) 2002-08-01
NO20032798L (no) 2003-08-19
DE60139511D1 (de) 2009-09-17
RU2003121306A (ru) 2005-03-10
ZA200304304B (en) 2004-09-02
HUP0303530A2 (hu) 2004-01-28
EE200300303A (et) 2003-12-15
PL366627A1 (en) 2005-02-07
WO2002059124A3 (en) 2004-01-08
CZ20031707A3 (cs) 2003-11-12
EP1399445A2 (en) 2004-03-24
BG107863A (en) 2004-06-30
EP1399445B9 (en) 2010-07-21
IS6851A (is) 2003-06-18
SK7032003A3 (en) 2004-04-06
BR0116348A (pt) 2004-11-23
JP2004528290A (ja) 2004-09-16
AU2002246726B2 (en) 2007-03-01
ATE438646T1 (de) 2009-08-15
US6777406B2 (en) 2004-08-17
WO2002059124A2 (en) 2002-08-01

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