ES2618939T3 - Sal de camsilato - Google Patents

Sal de camsilato Download PDF

Info

Publication number
ES2618939T3
ES2618939T3 ES13733415.7T ES13733415T ES2618939T3 ES 2618939 T3 ES2618939 T3 ES 2618939T3 ES 13733415 T ES13733415 T ES 13733415T ES 2618939 T3 ES2618939 T3 ES 2618939T3
Authority
ES
Spain
Prior art keywords
mol
strong
indene
mixture
salt
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
ES13733415.7T
Other languages
English (en)
Spanish (es)
Inventor
Martin Hans Bohlin
Craig Robert Stewart
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AstraZeneca AB
Original Assignee
AstraZeneca AB
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 AstraZeneca AB filed Critical AstraZeneca AB
Application granted granted Critical
Publication of ES2618939T3 publication Critical patent/ES2618939T3/es
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • C07D401/02Heterocyclic 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
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • 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
    • A61K31/4439Non 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • 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
    • C07D401/02Heterocyclic 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
    • C07D401/10Heterocyclic 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 linked by a carbon chain containing aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Psychiatry (AREA)
  • Psychology (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)
ES13733415.7T 2012-06-21 2013-06-20 Sal de camsilato Active ES2618939T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261662592P 2012-06-21 2012-06-21
US201261662592P 2012-06-21
PCT/GB2013/051606 WO2013190302A1 (en) 2012-06-21 2013-06-20 Camsylate salt

Publications (1)

Publication Number Publication Date
ES2618939T3 true ES2618939T3 (es) 2017-06-22

Family

ID=48746084

Family Applications (1)

Application Number Title Priority Date Filing Date
ES13733415.7T Active ES2618939T3 (es) 2012-06-21 2013-06-20 Sal de camsilato

Country Status (42)

Country Link
US (1) US10548882B2 (enExample)
EP (2) EP2864316B1 (enExample)
JP (2) JP2015520221A (enExample)
KR (1) KR102123708B1 (enExample)
CN (2) CN104411697B (enExample)
AP (2) AP2017009693A0 (enExample)
AR (2) AR091495A1 (enExample)
AU (2) AU2013279109B2 (enExample)
BR (2) BR112014031531B1 (enExample)
CA (1) CA2875589C (enExample)
CL (1) CL2014003374A1 (enExample)
CO (1) CO7151486A2 (enExample)
CR (2) CR20140571A (enExample)
CY (1) CY1119505T1 (enExample)
DK (1) DK2864316T3 (enExample)
DO (1) DOP2014000268A (enExample)
EC (1) ECSP14032215A (enExample)
ES (1) ES2618939T3 (enExample)
HR (1) HRP20170359T1 (enExample)
HU (1) HUE033376T2 (enExample)
IL (1) IL236131A0 (enExample)
IN (1) IN2014DN10088A (enExample)
LT (1) LT2864316T (enExample)
MA (2) MA39259B1 (enExample)
ME (1) ME02633B (enExample)
MX (1) MX354214B (enExample)
NI (1) NI201400146A (enExample)
NZ (2) NZ727045A (enExample)
PE (1) PE20150670A1 (enExample)
PH (2) PH12014502803A1 (enExample)
PL (1) PL2864316T3 (enExample)
PT (1) PT2864316T (enExample)
RS (1) RS55815B1 (enExample)
RU (1) RU2638175C2 (enExample)
SG (1) SG11201407934UA (enExample)
SI (1) SI2864316T1 (enExample)
SM (1) SMT201700142T1 (enExample)
TN (1) TN2014000491A1 (enExample)
TW (2) TWI639591B (enExample)
UA (1) UA114196C2 (enExample)
WO (1) WO2013190302A1 (enExample)
ZA (1) ZA201500408B (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8415483B2 (en) 2010-12-22 2013-04-09 Astrazeneca Ab Compounds and their use as BACE inhibitors
US9650336B2 (en) 2011-10-10 2017-05-16 Astrazeneca Ab Mono-fluoro beta-secretase inhibitors
US9000182B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab 2H-imidazol-4-amine compounds and their use as BACE inhibitors
US9000185B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cycloalkyl ether compounds and their use as BACE inhibitors
US9000183B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cyclohexane-1,2′-indene-1′,2″-imidazol compounds and their use as BACE inhibitors
US9000184B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cyclohexane-1,2′-naphthalene-1′,2″-imidazol compounds and their use as BACE inhibitors
UY36347A (es) 2014-10-07 2016-04-01 Astrazeneca Ab Compuestos y su uso como inhibidores de bace
JP6546410B2 (ja) * 2015-02-23 2019-07-17 ローム株式会社 電力供給装置、acアダプタ、acチャージャ、電子機器および電力供給システム
TW201740944A (zh) 2016-03-15 2017-12-01 美國禮來大藥廠 組合療法
WO2017158064A1 (en) 2016-03-15 2017-09-21 Astrazeneca Ab Combination of a bace inhibitor and an antibody or antigen-binding fragment for the treatment of a disorder associated with the accumulation of amyloid beta
KR20210139335A (ko) * 2019-03-14 2021-11-22 아스트라제네카 아베 체중 감소를 위한 라나베세스타트

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100452491B1 (ko) * 2001-03-29 2004-10-12 한미약품 주식회사 신규한 결정형 암로디핀 캠실레이트 염 및 그의 제조방법
JP4273406B2 (ja) 2001-06-01 2009-06-03 小野薬品工業株式会社 アルドース還元酵素阻害剤を有効成分とする脱髄性疾患または脱髄を伴う疾患治療剤
US7592348B2 (en) 2003-12-15 2009-09-22 Schering Corporation Heterocyclic aspartyl protease inhibitors
DE602005017129D1 (de) 2004-03-22 2009-11-26 Lilly Co Eli Pyridyl-derivate und ihre verwendung als mglu5-rezeptorantagonisten
AU2006259572A1 (en) 2005-06-14 2006-12-28 Schering Corporation Aspartyl protease inhibitors
WO2007058601A1 (en) 2005-11-21 2007-05-24 Astrazeneca Ab Novel 2-amino-imidazole-4-one compounds and their use in the manufacture of a medicament to be used in the treatment of cognitive impairment, alzheimer’s disease, neurodegeneration and dementia
TW200734311A (en) * 2005-11-21 2007-09-16 Astrazeneca Ab New compounds
CA2633992A1 (en) 2005-12-21 2007-07-05 Boehringer Ingelheim International Gmbh Pyrimidine derivatives useful as inhibitors of pkc-theta
WO2007100536A1 (en) 2006-02-24 2007-09-07 Wyeth DIHYDROSPIRO[DIBENZO[A,D][7]ANNULENE-5,4'-IMIDAZOL] COMPOUNDS FOR THE INHIBITION OF β-SECRETASE
WO2007146225A2 (en) 2006-06-12 2007-12-21 Schering Corporation Heterocyclic aspartyl protease inhibitors
WO2008076043A1 (en) 2006-12-20 2008-06-26 Astrazeneca Ab Novel 2-amino-5,5-diaryl-imidazol-4-ones
JP2010517963A (ja) 2007-02-01 2010-05-27 グラクソ グループ リミテッド 神経学的および神経精神病学的障害の治療におけるGlyT1トランスポーター阻害薬としての8−オキサ−1,4−ジアザスピロ[4,5]デク−3−エン−1−イルおよび1,4,8−トリアザスピロ[4,5]デク−3−エン−1−イルアセトアミド誘導体
MX2009012177A (es) 2007-05-07 2009-11-23 Schering Corp Moduladores de gamma-secretasa.
EP2249646A4 (en) 2008-02-06 2013-09-25 Glaxo Group Ltd PDE4 muscarinic Antagonist-DOPPELPHARMACOPHOREN
FR2929943B1 (fr) * 2008-04-15 2010-09-24 Inst Rech Developpement Ird Sels de quinoleines 2-substituees
AU2009277485B2 (en) 2008-07-28 2013-05-02 Eisai R&D Management Co., Ltd. Spiroaminodihydrothiazine derivatives
US8450308B2 (en) 2008-08-19 2013-05-28 Vitae Pharmaceuticals, Inc. Inhibitors of beta-secretase
TWI385175B (zh) 2008-09-11 2013-02-11 Amgen Inc 作為β-分泌酶調節劑之螺旋-三環化合物及其使用方法
AU2010223937B2 (en) 2009-03-13 2015-01-22 Vitae Pharmaceuticals, Inc. Inhibitors of beta-secretase
TW201103893A (en) 2009-07-02 2011-02-01 Astrazeneca Ab New compounds
AR077447A1 (es) 2009-07-02 2011-08-31 Astrazeneca Ab Compuestos inhibidores de beta-secretasa, utiles para el tratamiento de enfermedades neurodegenerativas
WO2011106414A1 (en) 2010-02-24 2011-09-01 Dillard Lawrence W Inhibitors of beta-secretase
US20120065195A1 (en) 2010-03-31 2012-03-15 Clark Christopher T Compounds for treating neurodegenerative diseases
WO2011130741A1 (en) 2010-04-16 2011-10-20 Array Biopharma Inc. Compounds for treating neurodegenerative diseases
WO2012019056A1 (en) 2010-08-05 2012-02-09 Amgen Inc. Amino-iso-indole, amino-aza-iso-indole, amino-dihydroisoquinoline and amino-benzoxazine compounds as beta-secretase modulators and methods of use
AR083169A1 (es) 2010-09-24 2013-02-06 Array Biopharma Inc Compuestos para tratar enfermedades neurodegenerativas
TW201307357A (zh) 2010-11-22 2013-02-16 Array Biopharma Inc 治療神經退化性疾病之化合物
US8415483B2 (en) * 2010-12-22 2013-04-09 Astrazeneca Ab Compounds and their use as BACE inhibitors
US9650336B2 (en) 2011-10-10 2017-05-16 Astrazeneca Ab Mono-fluoro beta-secretase inhibitors
US9000185B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cycloalkyl ether compounds and their use as BACE inhibitors
US9000183B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cyclohexane-1,2′-indene-1′,2″-imidazol compounds and their use as BACE inhibitors
US9000184B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab Cyclohexane-1,2′-naphthalene-1′,2″-imidazol compounds and their use as BACE inhibitors
US9000182B2 (en) 2012-06-20 2015-04-07 Astrazeneca Ab 2H-imidazol-4-amine compounds and their use as BACE inhibitors

Also Published As

Publication number Publication date
CN104411697A (zh) 2015-03-11
TW201406745A (zh) 2014-02-16
AU2017254965A1 (en) 2017-11-23
DK2864316T3 (en) 2017-03-20
AU2013279109B2 (en) 2017-08-31
AP2017009693A0 (en) 2017-01-31
PH12014502803B1 (en) 2015-02-23
CL2014003374A1 (es) 2015-02-27
US20140031379A1 (en) 2014-01-30
TWI639591B (zh) 2018-11-01
RS55815B1 (sr) 2017-08-31
CR20160202A (es) 2016-07-26
DOP2014000268A (es) 2015-04-15
NZ702742A (en) 2016-12-23
BR112014031531A2 (pt) 2017-06-27
MX2014014709A (es) 2015-03-04
CO7151486A2 (es) 2014-12-29
CR20140571A (es) 2015-02-04
US10548882B2 (en) 2020-02-04
MA39259A1 (fr) 2017-12-29
NI201400146A (es) 2016-09-21
LT2864316T (lt) 2017-03-27
JP2015520221A (ja) 2015-07-16
CN106279102A (zh) 2017-01-04
AU2017254965B2 (en) 2019-05-09
WO2013190302A1 (en) 2013-12-27
CN104411697B (zh) 2016-08-10
ECSP14032215A (es) 2015-12-31
AR091495A1 (es) 2015-02-11
ZA201500408B (en) 2016-10-26
SI2864316T1 (sl) 2017-04-26
KR102123708B1 (ko) 2020-06-16
MA39259B1 (fr) 2018-09-28
AR105176A2 (es) 2017-09-13
EP2864316B1 (en) 2016-12-14
PE20150670A1 (es) 2015-06-03
PL2864316T3 (pl) 2017-09-29
PH12014502803A1 (en) 2015-02-23
TN2014000491A1 (en) 2016-03-30
CY1119505T1 (el) 2018-03-07
AP2014008137A0 (en) 2014-12-31
PT2864316T (pt) 2017-02-24
BR112014031531B1 (pt) 2022-08-02
BR122016014302A2 (pt) 2019-08-27
KR20150023388A (ko) 2015-03-05
PH12016500498A1 (en) 2017-04-10
IL236131A0 (en) 2015-02-01
SMT201700142T1 (it) 2017-05-08
BR122016014302B1 (pt) 2022-08-23
TW201730177A (zh) 2017-09-01
MX354214B (es) 2018-02-19
TWI588140B (zh) 2017-06-21
MA37666B1 (fr) 2016-12-30
EP2864316A1 (en) 2015-04-29
HK1206349A1 (en) 2016-01-08
JP6509393B2 (ja) 2019-05-08
SG11201407934UA (en) 2015-01-29
HUE033376T2 (en) 2017-11-28
RU2638175C2 (ru) 2017-12-12
JP2018104448A (ja) 2018-07-05
RU2014148305A (ru) 2016-08-10
NZ727045A (en) 2018-06-29
ME02633B (me) 2017-06-20
HRP20170359T1 (hr) 2017-05-05
AU2013279109A1 (en) 2015-01-15
CA2875589A1 (en) 2013-12-27
IN2014DN10088A (enExample) 2015-08-21
UA114196C2 (uk) 2017-05-10
MA37666A1 (fr) 2016-04-29
CA2875589C (en) 2020-08-25
EP3064494A1 (en) 2016-09-07

Similar Documents

Publication Publication Date Title
ES2618939T3 (es) Sal de camsilato
AU2013326579B2 (en) 1,2,4-triazine derivatives for the treatment of viral infections.
ES2894262T3 (es) Procedimiento para preparar inhibidores de BTK
DK2970263T3 (en) PROCESSES FOR THE MANUFACTURE OF AN APOPTOSIS-PRACTICING EFFECT
JP7371221B2 (ja) Irak4キナーゼ阻害剤及びその調製方法
EP3414251B1 (en) Thienopyrazine carboxamides as ubiquitin-specific protease inhibitors
CN102421778A (zh) 二氢喋啶酮类衍生物、其制备方法及其在医药上的应用
EP3365340A1 (en) Heterocyclic compounds as immunomodulators
CA3009474A1 (en) Heterocyclic compounds as immunomodulators
CN116802179A (zh) Bcl-2抑制剂
WO2008139452A2 (en) Selective bromination of perylene diimides and derivatives thereof under mild conditions
WO2009112524A1 (en) Pyridopyrimidines as plk1 ( polo-like kinase) inhibitors
Palaniraja et al. UV-light induced domino type reactions: synthesis and photophysical properties of unreported nitrogen ring junction quinazolines
ES2902874T3 (es) Proceso químico para preparar derivados de imidazopirrolidinona y sus intermedios
EP4337221A1 (en) Silicone-based dyes and methods for making and using the same
WO2022148439A1 (zh) 作为bcl-2抑制剂的杂环化合物
JP6592521B2 (ja) ピラゾール誘導体の製造方法
CA3163528A1 (en) A method for preparing coumarin compounds substituted by amidoalkyl at 3-position, the products and related intermediates thereof
CN114057728A (zh) 作为bcl-2抑制剂的杂环化合物
Mayer et al. Synthesis of Benzobis [1, 3] oxathiins
Nuritdinova et al. Chemoselective Synthesis of Aminobenzylic Derivative of Mackinazolinone and its X-ray Investigations
WO2023230236A1 (en) Process for preparing jak inhibitors and intermediates thereof
Wang et al. Facile Synthesis of Novel N4-Substituted 2-(Trifluoromethyl)-tetrahydrobenzothieno [2, 3-d] pyrimidine Derivatives
Abashev et al. Bis (1, 3-dithiole-2-chalcogenones) and tetrathiafulvalenes in the synthesis of bridged tetrathiafulvalene-containing structures
ES2597976B1 (es) Método para la preparación de ácido 1-ciclopropil-6-fluoro-1,4-dihidro-8-metóxi-7-[(4as,7as)-octahidro-6h-pirrolo[3,4-b]piridin-6-il]- ]-4-oxo-3- quinolincarboxílico