CL2009002145A1 - Metodo de preparacion de derivados de pirrolidona utilizando la sintesis malonica; y los compuestos intermediarios considerados en el metodo. - Google Patents

Metodo de preparacion de derivados de pirrolidona utilizando la sintesis malonica; y los compuestos intermediarios considerados en el metodo.

Info

Publication number
CL2009002145A1
CL2009002145A1 CL2009002145A CL2009002145A CL2009002145A1 CL 2009002145 A1 CL2009002145 A1 CL 2009002145A1 CL 2009002145 A CL2009002145 A CL 2009002145A CL 2009002145 A CL2009002145 A CL 2009002145A CL 2009002145 A1 CL2009002145 A1 CL 2009002145A1
Authority
CL
Chile
Prior art keywords
preparation
pyrrolidone derivatives
compounds considered
intermediary compounds
malonic
Prior art date
Application number
CL2009002145A
Other languages
English (en)
Inventor
Rao Akireddy Srinivisa
Singh Bhatti Balwinder
J Cuthbertson Timothy
Harrison Miller Craig
Pike Mitchener Joseph Jr
Original Assignee
Targacept Inc
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 Targacept Inc filed Critical Targacept Inc
Publication of CL2009002145A1 publication Critical patent/CL2009002145A1/es

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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 hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • 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
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • 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
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • 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
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • 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
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • 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
    • C07D405/14—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 three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Transplantation (AREA)
  • Hematology (AREA)
  • Hospice & Palliative Care (AREA)
  • Rheumatology (AREA)
  • Virology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

Compuestos derivados de 3-etil-pirrolidina; y método de fabricación, útiles en la prevención o tratamiento de un trastorno mediado por los receptores nicotínicos neuronales.
CL2009002145A 2008-12-01 2009-11-30 Metodo de preparacion de derivados de pirrolidona utilizando la sintesis malonica; y los compuestos intermediarios considerados en el metodo. CL2009002145A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11888508P 2008-12-01 2008-12-01

Publications (1)

Publication Number Publication Date
CL2009002145A1 true CL2009002145A1 (es) 2010-04-30

Family

ID=41549744

Family Applications (2)

Application Number Title Priority Date Filing Date
CL2009002146A CL2009002146A1 (es) 2008-12-01 2009-11-30 Compuesto (r)-3-((e)-2-(pirrolidin-3-il)vinil)-5-(tetrahidropiran-4-iloxi)piridina y su sal mono-l-malato; su composicion farmaceutica; y su uso para el tratamiento de un trastorno mediado por nnr tal como trastornos del snc, inflamacion, trastornos inmunes, entre otros.
CL2009002145A CL2009002145A1 (es) 2008-12-01 2009-11-30 Metodo de preparacion de derivados de pirrolidona utilizando la sintesis malonica; y los compuestos intermediarios considerados en el metodo.

Family Applications Before (1)

Application Number Title Priority Date Filing Date
CL2009002146A CL2009002146A1 (es) 2008-12-01 2009-11-30 Compuesto (r)-3-((e)-2-(pirrolidin-3-il)vinil)-5-(tetrahidropiran-4-iloxi)piridina y su sal mono-l-malato; su composicion farmaceutica; y su uso para el tratamiento de un trastorno mediado por nnr tal como trastornos del snc, inflamacion, trastornos inmunes, entre otros.

Country Status (27)

Country Link
US (3) US8633227B2 (es)
EP (3) EP2358670B1 (es)
JP (2) JP5615836B2 (es)
KR (2) KR20110094318A (es)
CN (2) CN102232072B (es)
AR (1) AR074239A1 (es)
AU (2) AU2009322628A1 (es)
BR (2) BRPI0922152A2 (es)
CA (2) CA2744197A1 (es)
CL (2) CL2009002146A1 (es)
CO (1) CO6382158A2 (es)
EA (1) EA021054B1 (es)
EC (1) ECSP11011135A (es)
ES (1) ES2403022T3 (es)
IL (2) IL212796A0 (es)
MX (2) MX2011005713A (es)
MY (1) MY159040A (es)
NZ (1) NZ593058A (es)
PE (1) PE20100467A1 (es)
RU (1) RU2507197C2 (es)
SA (1) SA109300715B1 (es)
SG (2) SG171432A1 (es)
TW (1) TW201024283A (es)
UA (1) UA106217C2 (es)
UY (1) UY32278A (es)
WO (2) WO2010065449A1 (es)
ZA (1) ZA201103497B (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010065443A1 (en) * 2008-12-01 2010-06-10 Targacept, Inc. Synthesis and novel salt forms of (r)-5-((e)-2-(pyrrolidin-3-ylvinyl)pyrimidine
US9145396B2 (en) 2008-12-01 2015-09-29 Targacept, Inc. Synthesis and novel salt forms of (R)-5-((E)-2-pyrrolidin-3ylvinyl)pyrimidine
US20130196340A1 (en) * 2012-01-30 2013-08-01 Roar Holding Llc Ex vivo plasma enzyme activity assay using inhibitors as a negative control
AP2015008579A0 (en) 2013-02-05 2015-07-31 Purdue Pharma Lp Tamper resistant pharmaceutical formulations
US20160262372A1 (en) * 2015-03-13 2016-09-15 Cornell Kunz Extermination Treatment Appliance And Method
CN114533737B (zh) 2016-04-07 2024-05-31 奥伊斯特普安生物制药公司 治疗眼部病状的方法

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SK94393A3 (en) * 1992-09-11 1994-08-10 Thomae Gmbh Dr K Cyclic derivatives of urea, process for their production and their pharmaceutical agents with the content of those
IL107184A (en) 1992-10-09 1997-08-14 Abbott Lab Heterocyclic ether compounds that enhance cognitive function
US5852041A (en) 1993-04-07 1998-12-22 Sibia Neurosciences, Inc. Substituted pyridines useful as modulators of acethylcholine receptors
US5604231A (en) 1995-01-06 1997-02-18 Smith; Carr J. Pharmaceutical compositions for prevention and treatment of ulcerative colitis
US5597919A (en) 1995-01-06 1997-01-28 Dull; Gary M. Pyrimidinyl or Pyridinyl alkenyl amine compounds
JP3745433B2 (ja) * 1995-02-02 2006-02-15 第一製薬株式会社 複素環式化合物
US5585388A (en) 1995-04-07 1996-12-17 Sibia Neurosciences, Inc. Substituted pyridines useful as modulators of acetylcholine receptors
US5583140A (en) 1995-05-17 1996-12-10 Bencherif; Merouane Pharmaceutical compositions for the treatment of central nervous system disorders
IL118279A (en) 1995-06-07 2006-10-05 Abbott Lab Compounds 3 - Pyridyloxy (or Thio) Alkyl Heterocyclic Pharmaceutical Compositions Containing Them and Their Uses for Preparing Drugs to Control Synaptic Chemical Transmission
PL332240A1 (en) * 1996-09-13 1999-08-30 Schering Corp Tricyclic compounds useful in inhibiting g-proteinic function and in treating proliferative diseases
TW492957B (en) * 1996-11-07 2002-07-01 Novartis Ag N-substituted 2-cyanopyrrolidnes
ZA9711092B (en) 1996-12-11 1999-07-22 Smithkline Beecham Corp Novel compounds.
JPH1171345A (ja) * 1997-08-30 1999-03-16 Nippon Nohyaku Co Ltd 光学活性なピロリジン誘導体及びその中間体並びにそれらの製造法
US6310043B1 (en) 1998-08-07 2001-10-30 Governors Of The University Of Alberta Treatment of bacterial infections
GB9821503D0 (en) 1998-10-02 1998-11-25 Novartis Ag Organic compounds
CA2415468A1 (en) * 2000-07-11 2003-01-10 Yoshio Ogino Ester derivatives
WO2003013526A1 (en) * 2001-08-08 2003-02-20 Merck & Co. Inc. Anticoagulant compounds
US7098331B2 (en) * 2003-03-05 2006-08-29 Targacept, Inc. Arylvinylazacycloalkane compounds and methods of preparation and use thereof
WO2007054777A1 (en) * 2005-11-09 2007-05-18 Orchid Chemicals & Pharmaceuticals Limited Depletion of isomer in cephalosporin antibiotic
WO2007134298A2 (en) * 2006-05-12 2007-11-22 Myriad Genetics, Inc. Therapeutic compounds and their use in cancer

Also Published As

Publication number Publication date
IL212799A (en) 2013-12-31
EA201170736A1 (ru) 2011-12-30
AU2009322628A1 (en) 2010-06-10
CO6382158A2 (es) 2012-02-15
US20110269975A1 (en) 2011-11-03
EA021054B1 (ru) 2015-03-31
EP2358670A2 (en) 2011-08-24
HK1157778A1 (en) 2012-07-06
MY159040A (en) 2016-12-15
CN102227406A (zh) 2011-10-26
RU2011127004A (ru) 2013-01-10
MX2011005712A (es) 2011-06-17
US20120015983A1 (en) 2012-01-19
ECSP11011135A (es) 2011-07-29
CN102227406B (zh) 2013-07-31
CA2744191A1 (en) 2010-06-10
AU2009322630A1 (en) 2010-06-10
JP5698673B2 (ja) 2015-04-08
ZA201103497B (en) 2012-01-25
AR074239A1 (es) 2010-12-29
SA109300715B1 (ar) 2014-06-25
RU2507197C2 (ru) 2014-02-20
JP2012510473A (ja) 2012-05-10
WO2010065447A3 (en) 2010-07-22
EP2358705A1 (en) 2011-08-24
WO2010065447A2 (en) 2010-06-10
SG171876A1 (en) 2011-07-28
US8153821B2 (en) 2012-04-10
KR20110094318A (ko) 2011-08-23
KR20110094100A (ko) 2011-08-19
UA106217C2 (en) 2014-08-11
PE20100467A1 (es) 2010-08-03
CN102232072B (zh) 2014-09-24
MX2011005713A (es) 2011-06-17
JP5615836B2 (ja) 2014-10-29
US20140107163A1 (en) 2014-04-17
CA2744197A1 (en) 2010-06-10
WO2010065449A1 (en) 2010-06-10
BRPI0922152A2 (pt) 2015-08-18
TW201024283A (en) 2010-07-01
NZ593058A (en) 2013-06-28
UY32278A (es) 2011-06-30
IL212799A0 (en) 2011-07-31
US8633227B2 (en) 2014-01-21
BRPI0922630A2 (pt) 2016-01-05
CN102232072A (zh) 2011-11-02
EP2358670B1 (en) 2012-10-24
CL2009002146A1 (es) 2010-04-30
EP2896619A1 (en) 2015-07-22
SG171432A1 (en) 2011-07-28
IL212796A0 (en) 2011-07-31
ES2403022T3 (es) 2013-05-13
JP2012510472A (ja) 2012-05-10

Similar Documents

Publication Publication Date Title
LTC2937350I2 (lt) 1'-pakeistieji karba-nukleozidų analogai, skirti antivirusiniam gydymui
NO20090879L (no) Titandioksidinneholdende kompositt
DK2300443T3 (da) Triazolderivater, der er anvendelige til behandling af sygdomme
EA201001135A1 (ru) Интратекальное лечение невропатической боли агонистами ar
MY146506A (en) Substituted pyridyl amide compounds as modulators of the histamine h3 receptor
EA201001847A1 (ru) Соединения и композиции, применяемые для лечения малярии
MX2009009415A (es) Compuestos de tetrahidroisoquinolina como moduladores del receptor h3 de la histamina.
MX2010008714A (es) Derivados de amida como moduladores alostericos positivos y metodos de uso de los mismos.
EA201170753A1 (ru) Налмефена гидрохлорид дигидрат
MX2010009003A (es) Ciclohexanodimetanamina por aminacion directa de ciclohexanodimetanol.
EP1991253A4 (en) NERVE REGENERATION WITH KERATIN BIOMATERIAL
WO2008124129A3 (en) Treating hiv with a m-csf effector kinase inhibitor like imatinib
CR20110202A (es) Antagonistas de la via hedgehog de ftalazina disustituida
WO2009145996A3 (en) Amide derivatives as positive allosteric modulators and methods of use thereof
CL2009002145A1 (es) Metodo de preparacion de derivados de pirrolidona utilizando la sintesis malonica; y los compuestos intermediarios considerados en el metodo.
MX2011006843A (es) Dihidropiridona-amidas como moduladores de p2x7.
BRPI0923316A2 (pt) método, e método de tratar uma formação penetrada por um poço.
BRPI0820440A2 (pt) Inibidores aldh-2 no tratamento de desordens psiquiátricas
EP2334316A4 (en) PROCESS FOR SYNTHESIS OF - (AIB8,35) HGLP-1 (7-36) -NH2
MX2010002506A (es) Compuestos de nicotinamida sustituidos y uso de estos en medicamentos.
UA103468C2 (ru) Соединения циклоалкилокси- и гетероциклоалкилоксипиридина как модуляторы гистаминового рецептора н3
CR10036A (es) Procedimientos para la preparación de derivados de ciclopropilamida
NO20091521L (no) Polycykliske midler forbehandling av respiratoriske syncytiale virusinfeksjoner
BRPI0821026A2 (pt) Derivados de alfa-minoamidas úteis no tratamento de transtornos psiquiátricos
EA201001828A1 (ru) Способ синтеза производных 3,6-дигидро-1,3,5-триазина