BR9809162A - Sal de trans-5-cloro-2, 3, 3a, 12b-tetrahidro-2-metil-1h-dibenz [2,3:6,7] oxepino[4,5-c] pirrol e agente formador de sal, composto, composição farmacêutica, e, preparação de injeção armazenável - Google Patents

Sal de trans-5-cloro-2, 3, 3a, 12b-tetrahidro-2-metil-1h-dibenz [2,3:6,7] oxepino[4,5-c] pirrol e agente formador de sal, composto, composição farmacêutica, e, preparação de injeção armazenável

Info

Publication number
BR9809162A
BR9809162A BR9809162-0A BR9809162A BR9809162A BR 9809162 A BR9809162 A BR 9809162A BR 9809162 A BR9809162 A BR 9809162A BR 9809162 A BR9809162 A BR 9809162A
Authority
BR
Brazil
Prior art keywords
salt
tetrahydro
trans
methyl
forming agent
Prior art date
Application number
BR9809162-0A
Other languages
English (en)
Inventor
Gerardus Johannes Heeres
Franciscus Hermanus Anto Bakel
Original Assignee
Akzo Nobel Nv
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 Akzo Nobel Nv filed Critical Akzo Nobel Nv
Publication of BR9809162A publication Critical patent/BR9809162A/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • 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
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

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

Abstract

''SAL DE TRANS-5-CLORO-2,3,3A,12B-TETRAHIDRO-2-METIL-1H-DIBEN Z[2,3:6,7]OXEPINO[4,5-C]PIRROL E AGENTE FORMADOR DE SAL, COMPOSTO, COMPOSIçãO FARMACêUTICA, E, PREPARAçãO DE INJEçãO ARMAZENáVEL'' A invenção é um sal do CNS-depressor, trans-5- cloro-2,3,3a,12b-tetrahidro-2- metil-1H-dibenz[2,3:6,7} oxepino[4,5-c]pirrol e um agente formador de sal, este último sendo um ácido sulfónico aromático. O sal descoberto, de preferência o besilato, tem propriedades favoráveis. Desse modo, ele apresenta a insolubilidade e a cristalinidade necessárias, adequando-se ao uso em preparações de injeção armazenáveis.
BR9809162-0A 1997-05-26 1998-05-19 Sal de trans-5-cloro-2, 3, 3a, 12b-tetrahidro-2-metil-1h-dibenz [2,3:6,7] oxepino[4,5-c] pirrol e agente formador de sal, composto, composição farmacêutica, e, preparação de injeção armazenável BR9809162A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP97201596 1997-05-26
PCT/EP1998/003022 WO1998054186A1 (en) 1997-05-26 1998-05-19 Salts of aromatic sulphonic acids

Publications (1)

Publication Number Publication Date
BR9809162A true BR9809162A (pt) 2000-08-01

Family

ID=8228372

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9809162-0A BR9809162A (pt) 1997-05-26 1998-05-19 Sal de trans-5-cloro-2, 3, 3a, 12b-tetrahidro-2-metil-1h-dibenz [2,3:6,7] oxepino[4,5-c] pirrol e agente formador de sal, composto, composição farmacêutica, e, preparação de injeção armazenável

Country Status (12)

Country Link
EP (1) EP0984968A1 (pt)
JP (1) JP2001526702A (pt)
KR (1) KR20010012985A (pt)
CN (1) CN1257504A (pt)
AU (1) AU7767598A (pt)
BR (1) BR9809162A (pt)
CA (1) CA2290070A1 (pt)
HU (1) HUP0002106A3 (pt)
NO (1) NO995770D0 (pt)
PL (1) PL337027A1 (pt)
TR (1) TR199902727T2 (pt)
WO (1) WO1998054186A1 (pt)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5067998B2 (ja) 2001-10-30 2012-11-07 ノバルティス アーゲー イロペリドンおよび星形ポリマーのデポー製剤
HRP20020440B1 (en) 2002-05-21 2008-02-29 GlaxoSmithKline istra�iva�ki centar Zagreb d.o.o. 1-aza-dibenzoazulenes as inhibitors of tumor necrosis factor production and intermediates for the preparation thereof
HRP20020452A2 (en) 2002-05-23 2004-02-29 Pliva D D 1,2-diaza-dibenzoazulen as inhibitor of production of tumor necrosis factors and intermediates for preparation thereof
GB0216416D0 (en) 2002-07-15 2002-08-21 Novartis Ag Organic compounds
EP1802301A1 (en) * 2004-10-15 2007-07-04 Pfizer Inc. Treatment of bipolar disorders and associated symptoms
JP5801295B2 (ja) 2009-06-24 2015-10-28 メルク・シャープ・エンド・ドーム・ベー・フェー アセナピンを含有する注射可能な配合物およびそれを用いた処置方法
ITMI20110734A1 (it) 2011-05-02 2012-11-03 Olon Spa Sali cristallini di asenapina
EP2524919A1 (en) 2011-05-17 2012-11-21 Sandoz AG Novel crystalline salts of Asenapine with organic Di-acids and Tri-acids
EP2524920A1 (en) 2011-05-17 2012-11-21 Sandoz AG Novel Crystalline Asenapine Hydrochloride Salt Forms
EP2524921A1 (en) 2011-05-17 2012-11-21 Sandoz AG Novel Crystalline Salts of Asenapine
AU2017384526B2 (en) 2016-12-20 2023-11-02 Lts Lohmann Therapie-Systeme Ag Transdermal therapeutic system containing asenapine
US11337932B2 (en) 2016-12-20 2022-05-24 Lts Lohmann Therapie-Systeme Ag Transdermal therapeutic system containing asenapine and polysiloxane or polyisobutylene
US11033512B2 (en) 2017-06-26 2021-06-15 Lts Lohmann Therapie-Systeme Ag Transdermal therapeutic system containing asenapine and silicone acrylic hybrid polymer
CN112704672A (zh) 2018-06-20 2021-04-27 罗曼治疗系统股份公司 含有阿塞那平的透皮治疗系统

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL7605526A (nl) * 1976-05-24 1977-11-28 Akzo Nv Nieuwe tetracyclische derivaten.

Also Published As

Publication number Publication date
AU7767598A (en) 1998-12-30
NO995770L (no) 1999-11-25
HUP0002106A3 (en) 2001-11-28
PL337027A1 (en) 2000-07-31
JP2001526702A (ja) 2001-12-18
CN1257504A (zh) 2000-06-21
TR199902727T2 (xx) 2000-07-21
NO995770D0 (no) 1999-11-25
HUP0002106A2 (hu) 2000-11-28
WO1998054186A1 (en) 1998-12-03
EP0984968A1 (en) 2000-03-15
CA2290070A1 (en) 1998-12-03
KR20010012985A (ko) 2001-02-26

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Legal Events

Date Code Title Description
FA10 Dismissal: dismissal - article 33 of industrial property law
B11Y Definitive dismissal - extension of time limit for request of examination expired [chapter 11.1.1 patent gazette]