ECSP067100A - Preparación enantioselectiva del derivado de quinolina - Google Patents

Preparación enantioselectiva del derivado de quinolina

Info

Publication number
ECSP067100A
ECSP067100A EC2006007100A ECSP067100A ECSP067100A EC SP067100 A ECSP067100 A EC SP067100A EC 2006007100 A EC2006007100 A EC 2006007100A EC SP067100 A ECSP067100 A EC SP067100A EC SP067100 A ECSP067100 A EC SP067100A
Authority
EC
Ecuador
Prior art keywords
quinoline derivative
quinolin
oxy
substituted
enantioselective preparation
Prior art date
Application number
EC2006007100A
Other languages
English (en)
Inventor
Olivier Lohse
Caspar Vogel
Gerhard Penn
Original Assignee
Novartis Ag
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=32799952&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ECSP067100(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of ECSP067100A publication Critical patent/ECSP067100A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/20Oxygen atoms
    • C07D215/24Oxygen atoms attached in position 8
    • C07D215/26Alcohols; Ethers thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/20Oxygen atoms
    • C07D215/24Oxygen atoms attached in position 8
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/04Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D251/06Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pulmonology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Se describe un proceso para la preparación de oxi-5-((R)-2-halo-1-hidroxi-etil)-(1H)-quinolin-2-onas 8-sustituidas, o solvatos aceptables de las mismas. El proceso involucra hacer reaccionar una oxi-(1H)-quinolin-2-ona 5-(a-haloacetil)-8-sustituida con un agente reductor en la presencia de un agente quiral y una base, para formar una 8-(oxi-sustituida)-5-((R)-2-halo-1-hidroxi-etil)-(1H)-quinolin-2-ona, el agente quiral una Fórmula I ó II:donde M, L, X, R1, R2, y R3 tienen los significados indicados en la especificación.
EC2006007100A 2004-06-22 2006-12-20 Preparación enantioselectiva del derivado de quinolina ECSP067100A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0413960.6A GB0413960D0 (en) 2004-06-22 2004-06-22 Organic compounds

Publications (1)

Publication Number Publication Date
ECSP067100A true ECSP067100A (es) 2007-01-26

Family

ID=32799952

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2006007100A ECSP067100A (es) 2004-06-22 2006-12-20 Preparación enantioselectiva del derivado de quinolina

Country Status (32)

Country Link
US (2) US20090054653A1 (es)
EP (1) EP1791820B1 (es)
JP (1) JP5064214B2 (es)
KR (1) KR101179302B1 (es)
CN (1) CN1968927B (es)
AR (2) AR049553A1 (es)
AT (1) ATE450512T1 (es)
AU (1) AU2005254698B2 (es)
BR (1) BRPI0512298A (es)
CA (1) CA2566388C (es)
CY (1) CY1109884T1 (es)
DE (1) DE602005018076D1 (es)
DK (1) DK1791820T3 (es)
EC (1) ECSP067100A (es)
ES (1) ES2337273T3 (es)
GB (1) GB0413960D0 (es)
HR (1) HRP20100087T1 (es)
IL (1) IL179600A (es)
MA (1) MA28687B1 (es)
MX (1) MXPA06014695A (es)
MY (1) MY142051A (es)
NO (1) NO339079B1 (es)
NZ (1) NZ551276A (es)
PE (1) PE20060304A1 (es)
PL (1) PL1791820T3 (es)
PT (1) PT1791820E (es)
RU (1) RU2383534C2 (es)
SI (1) SI1791820T1 (es)
TN (1) TNSN06408A1 (es)
TW (1) TWI347317B (es)
WO (1) WO2005123684A2 (es)
ZA (1) ZA200609257B (es)

Families Citing this family (33)

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BRPI0713951B8 (pt) 2006-06-30 2021-05-25 Novartis Ag derivados de quinazolina, e composição farmacêutica
EP1914227A1 (en) * 2006-08-31 2008-04-23 Novartis AG Polymorphic crystal form of a indan-2-ylamino-hydroxyethyl-quinolinone maleate derivative as beta-adrenoceptor agonist
WO2011056929A1 (en) 2009-11-04 2011-05-12 Massachusetts Institute Of Technology Continuous flow synthesis of amino alcohols using microreactors
WO2011109276A1 (en) 2010-03-01 2011-09-09 Massachussets Institute Of Technology Epoxidation catalysts
MA34373B1 (fr) 2010-07-14 2013-07-03 Novartis Ag Composés hétérocycliques agonistes du récepteur ip
JOP20120023B1 (ar) 2011-02-04 2022-03-14 Novartis Ag صياغات مساحيق جافة من جسيمات تحتوي على واحد أو اثنين من المواد الفعالة لعلاج امراض ممرات الهواء الانسدادية او الالتهابية
US20140378463A1 (en) 2012-01-13 2014-12-25 Novartis Ag IP receptor agonist heterocyclic compounds
JP6058698B2 (ja) 2012-01-13 2017-01-11 ノバルティス アーゲー Ip受容体アゴニストの塩
ES2565826T3 (es) 2012-01-13 2016-04-07 Novartis Ag Pirroles fusionados como agonistas del receptor IP para el tratamiento de hipertensión arterial pulmonar (PAH) y trastornos relacionados
US20150005311A1 (en) 2012-01-13 2015-01-01 Novartis Ag IP receptor agonist heterocyclic compounds
WO2013105065A1 (en) 2012-01-13 2013-07-18 Novartis Ag Fused piperidines as ip receptor agonists for the treatment of pah and related disorders
WO2013105061A1 (en) 2012-01-13 2013-07-18 Novartis Ag Fused dihydropyrido [2,3 -b] pyrazines as ip receptor agonists for the treatment of pulmonary arterial hypertension (pah) and related disorders
CN104379566B (zh) * 2012-07-11 2016-08-24 上海威智医药科技有限公司 茚达特罗中间体及茚达特罗的合成方法
EP3848354B1 (en) 2012-09-21 2022-07-27 Crystal Pharma, S.A.U. Process for the preparation of indacaterol and intermediates thereof
WO2014044288A1 (en) 2012-09-21 2014-03-27 Crystal Pharma Sa Methods for the preparation of indacaterol and pharmaceutically acceptable salts thereof
ES2715682T3 (es) 2012-12-19 2019-06-05 Novartis Ag Inhibidores de la autotaxina
US9604981B2 (en) 2013-02-13 2017-03-28 Novartis Ag IP receptor agonist heterocyclic compounds
CA2898700C (en) 2013-03-14 2022-07-19 Novartis Ag Deamorphization of spray-dried formulations via spray-blending
US9452139B2 (en) 2013-03-14 2016-09-27 Novartis Ag Respirable agglomerates of porous carrier particles and micronized drug
CZ306252B6 (cs) 2013-03-15 2016-10-26 Zentiva, K.S. Způsob přípravy 5-[(R)-2-(5,6-diethylindan-2-ylamino)-1-hydroxyethyl]-8-hydroxy-(1H)-chinolin-2-onu (indacaterolu)
EP2978745B1 (en) 2013-03-27 2017-03-15 Laboratorios Lesvi, S.L. Process for the manufacture of (r)-5-[2-(5,6-diethylindan-2-ylamino)-1-hydroxyethyl]-8-hydroxy-(1h)-quinolin-2-one
EP3022201A1 (en) 2013-07-18 2016-05-25 Novartis AG Autotaxin inhibitors
MX368059B (es) 2013-07-18 2019-09-18 Novartis Ag Inhibidores de autotaxina que comprenden un núcleo de anillo heteroaromático de bencil-amida cíclica.
EP3092217B1 (en) 2014-01-09 2020-06-03 Davuluri, Ramamohan Rao A novel process for preparation of indacaterol or its pharmaceutically acceptable salts
EP3122331A1 (en) 2014-03-27 2017-02-01 Novartis AG Spray-dried solid-in-oil-in-water dispersions for inhalation of active pharmaceutical ingredients
EP3134398A1 (en) 2014-04-24 2017-03-01 Novartis Ag Autotaxin inhibitors
CN105693603B (zh) * 2014-11-24 2019-11-29 上海医药工业研究院 改良的马来酸茚达特罗制备工艺
KR101769204B1 (ko) * 2015-08-04 2017-08-17 씨제이헬스케어 주식회사 크로마놀 유도체의 신규한 제조방법
ES2747905T3 (es) 2015-09-29 2020-03-12 Inke Sa Solvato mixto de L-tartrato de (R)-5-[2-(5,6-dietilindan-2-ilamino)-1-hidroxietil]-8-hidroxi-1H-quinolin-2-ona
JP6621442B2 (ja) * 2016-05-17 2019-12-18 財團法人工業技術研究院Industrial Technology Research Institute 金属イオンバッテリー
CN107868045A (zh) * 2016-09-28 2018-04-03 四川海思科制药有限公司 一种茚达特罗中间体的制备方法
CN114591236A (zh) * 2020-12-02 2022-06-07 四川海思科制药有限公司 一种茚达特罗的改进制备方法
CN113731406B (zh) * 2021-10-12 2023-07-28 南京工业大学 一种提高钯碳活性加氢脱除保护基的方法

Family Cites Families (6)

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Publication number Priority date Publication date Assignee Title
GB9405019D0 (en) 1994-03-15 1994-04-27 Smithkline Beecham Plc Novel compounds
TR199802385T2 (xx) * 1996-05-20 1999-04-21 Darwin Discovery Limited TNF inhibit�rleri ve FDE-IV inhibit�rleri olarak kinolin karboksamidler.
GB9913083D0 (en) * 1999-06-04 1999-08-04 Novartis Ag Organic compounds
TWI249515B (en) * 2001-11-13 2006-02-21 Theravance Inc Aryl aniline beta2 adrenergic receptor agonists
TWI324150B (en) * 2003-02-28 2010-05-01 Novartis Ag Process for preparing 5-[(r)-2-(5,6-diethyl-indan-2-ylamino)-1-hydroxy-ethyl]-8-hydroxy-(1h)-quinolin-2-one salt
PE20100399A1 (es) * 2003-04-02 2010-06-01 Novartis Ag Procedimiento para preparar oxi-(1h)-quinolin-2-onas 5-(alfa-haloacetil)-8-sustituidas

Also Published As

Publication number Publication date
AR049553A1 (es) 2006-08-16
DK1791820T3 (da) 2010-04-06
NO20070400L (no) 2007-03-21
NZ551276A (en) 2010-06-25
RU2383534C2 (ru) 2010-03-10
TNSN06408A1 (en) 2008-02-22
KR20070029752A (ko) 2007-03-14
EP1791820B1 (en) 2009-12-02
SI1791820T1 (sl) 2010-04-30
NO339079B1 (no) 2016-11-07
CY1109884T1 (el) 2014-09-10
ATE450512T1 (de) 2009-12-15
AU2005254698B2 (en) 2008-09-25
ZA200609257B (en) 2008-07-30
AR082981A2 (es) 2013-01-23
US20090054653A1 (en) 2009-02-26
CN1968927A (zh) 2007-05-23
IL179600A0 (en) 2007-05-15
DE602005018076D1 (de) 2010-01-14
KR101179302B1 (ko) 2012-09-03
CA2566388A1 (en) 2005-12-29
IL179600A (en) 2011-11-30
MA28687B1 (fr) 2007-06-01
MY142051A (en) 2010-08-30
HK1105121A1 (en) 2008-02-01
HRP20100087T1 (hr) 2010-06-30
PL1791820T3 (pl) 2010-05-31
GB0413960D0 (en) 2004-07-28
PE20060304A1 (es) 2006-05-19
TW200615265A (en) 2006-05-16
CN1968927B (zh) 2010-07-21
US20120220775A1 (en) 2012-08-30
PT1791820E (pt) 2010-02-23
WO2005123684A2 (en) 2005-12-29
BRPI0512298A (pt) 2008-03-25
CA2566388C (en) 2013-04-16
TWI347317B (en) 2011-08-21
WO2005123684A3 (en) 2006-06-01
JP5064214B2 (ja) 2012-10-31
MXPA06014695A (es) 2007-02-12
JP2008503526A (ja) 2008-02-07
RU2007102228A (ru) 2008-07-27
ES2337273T3 (es) 2010-04-22
AU2005254698A1 (en) 2005-12-29
EP1791820A2 (en) 2007-06-06

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