NO20072173L - Fremgangsmate for fremstilling av 4-{4-[({[4-klor-3-(trifluormetyl)fenyl]amino}karbonyl)amino] fenoksy}-N-metylpyridin-2-karboksamid - Google Patents

Fremgangsmate for fremstilling av 4-{4-[({[4-klor-3-(trifluormetyl)fenyl]amino}karbonyl)amino] fenoksy}-N-metylpyridin-2-karboksamid

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Publication number
NO20072173L
NO20072173L NO20072173A NO20072173A NO20072173L NO 20072173 L NO20072173 L NO 20072173L NO 20072173 A NO20072173 A NO 20072173A NO 20072173 A NO20072173 A NO 20072173A NO 20072173 L NO20072173 L NO 20072173L
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Norway
Prior art keywords
amino
chloro
formula
compound
methylpyridine
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NO20072173A
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English (en)
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NO339647B1 (no
Inventor
Matthias Mueller-Gliemann
Reinhold Gehring
Werner Heilmann
Mathias Berwe
Michael Loegers
Oliver Kuhn
Mike Matthaeus
Klaus Mohrs
Juergen Stiehl
Hana Lenz
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Bayer Healthcare Ag
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Application filed by Bayer Healthcare Ag filed Critical Bayer Healthcare Ag
Publication of NO20072173L publication Critical patent/NO20072173L/no
Publication of NO339647B1 publication Critical patent/NO339647B1/no

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/166Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
    • 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
    • A61K31/4412Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pyridine Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Developing Agents For Electrophotography (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Abstract

Foreliggende oppfinnelse angår en fremgangsmåte for fremstilling av 4-{4-[({ [4-kloro-3-(trifluorometyl)fenyl]arrrino}karbonyl)arnino]fenoksy}-Af-metylpyridin-2-karboksamid og dets tosylatsalt. Formel (I), som innbefatter, i et første trinn, omsetting av forbindelsen med formel (V) med 4-kloro-3-trifluorometylfenyl-isocyanat i et ikke-klorert organisk løsemiddel, inert overfor isocyanater, ved initielt å tilsette forbindelsen med formel (V) ved en temperatur på fra 20°C til 60°C og blande sammen med 4-kloro-3-trifluorometylfenyl-isocyanat på en slik måte at reaksjonstemperaturen ikke overskrider 70°C for å gi forbindelsen med formel (II) og, i et andre trinn, blande forbindelsen med formel (II) sammen med p-toluensulfonsyre i et polart løsemiddel ved en reaksjonstemperatur på fra 40°C og opp til reflukstemperaturen til anvendt løsemiddel.
NO20072173A 2004-09-29 2007-04-26 Fremgangsmåte for fremstilling av 4-{4-[({[4-kloro-3-(trifluorometyl)-fenyl]amino}karbonyl)amino]fenoksy}-N-metylpyridin-2-karboksamid og dets tosylatsalt NO339647B1 (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP04023131 2004-09-29
PCT/EP2005/010118 WO2006034796A1 (en) 2004-09-29 2005-09-20 Process for the preparation of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-n-methylpyridine-2-carboxamide

Publications (2)

Publication Number Publication Date
NO20072173L true NO20072173L (no) 2007-06-14
NO339647B1 NO339647B1 (no) 2017-01-16

Family

ID=35457568

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20072173A NO339647B1 (no) 2004-09-29 2007-04-26 Fremgangsmåte for fremstilling av 4-{4-[({[4-kloro-3-(trifluorometyl)-fenyl]amino}karbonyl)amino]fenoksy}-N-metylpyridin-2-karboksamid og dets tosylatsalt

Country Status (35)

Country Link
US (1) US8124782B2 (no)
EP (1) EP1797037B1 (no)
JP (2) JP2008514657A (no)
KR (1) KR101263032B1 (no)
CN (1) CN101052619B (no)
AR (1) AR053973A1 (no)
AU (1) AU2005289099B2 (no)
BR (1) BRPI0515944B1 (no)
CA (1) CA2581835C (no)
CU (1) CU23754B7 (no)
CY (1) CY1116126T1 (no)
DK (1) DK1797037T3 (no)
DO (1) DOP2005000183A (no)
EC (1) ECSP077357A (no)
ES (1) ES2532377T3 (no)
GT (1) GT200500269A (no)
HK (1) HK1113484A1 (no)
HN (1) HN2005000768A (no)
HR (1) HRP20150295T1 (no)
IL (1) IL182046A0 (no)
MA (1) MA28883B1 (no)
MY (1) MY149873A (no)
NO (1) NO339647B1 (no)
NZ (1) NZ554119A (no)
PE (5) PE20091586A1 (no)
PL (1) PL1797037T3 (no)
PT (1) PT1797037E (no)
SG (1) SG155997A1 (no)
SI (1) SI1797037T1 (no)
SV (1) SV2006002243A (no)
TW (1) TWI382973B (no)
UA (1) UA90691C2 (no)
UY (1) UY29143A1 (no)
WO (1) WO2006034796A1 (no)
ZA (1) ZA200702511B (no)

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CN104761492A (zh) * 2014-01-03 2015-07-08 正大天晴药业集团股份有限公司 对甲苯磺酸索拉非尼的晶型及其制备方法
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Also Published As

Publication number Publication date
EP1797037B1 (en) 2014-12-17
UA90691C2 (en) 2010-05-25
CU23754B7 (es) 2012-01-31
ECSP077357A (es) 2007-04-26
PL1797037T3 (pl) 2015-07-31
SI1797037T1 (sl) 2015-06-30
PE20060825A1 (es) 2006-10-20
CN101052619B (zh) 2012-02-22
CU20070069A7 (es) 2010-11-27
EP1797037A1 (en) 2007-06-20
DOP2005000183A (es) 2006-03-31
JP5583190B2 (ja) 2014-09-03
ES2532377T3 (es) 2015-03-26
TW200626551A (en) 2006-08-01
PT1797037E (pt) 2015-03-17
JP2008514657A (ja) 2008-05-08
PE20091584A1 (es) 2009-10-28
NO339647B1 (no) 2017-01-16
UY29143A1 (es) 2006-04-28
HK1113484A1 (en) 2008-10-03
BRPI0515944B1 (pt) 2021-11-09
NZ554119A (en) 2010-07-30
CN101052619A (zh) 2007-10-10
WO2006034796A1 (en) 2006-04-06
PE20091587A1 (es) 2009-11-05
SG155997A1 (en) 2009-10-29
MA28883B1 (fr) 2007-09-03
PE20091586A1 (es) 2009-10-31
AR053973A1 (es) 2007-05-30
SV2006002243A (es) 2006-10-13
KR20070058676A (ko) 2007-06-08
BRPI0515944A (pt) 2008-08-12
MY149873A (en) 2013-10-31
CY1116126T1 (el) 2017-02-08
HRP20150295T1 (hr) 2015-05-22
ZA200702511B (en) 2008-07-30
US8124782B2 (en) 2012-02-28
PE20091585A1 (es) 2009-10-31
KR101263032B1 (ko) 2013-05-09
DK1797037T3 (en) 2015-03-30
IL182046A0 (en) 2007-07-24
US20080262236A1 (en) 2008-10-23
AU2005289099A1 (en) 2006-04-06
GT200500269A (es) 2006-05-11
CA2581835A1 (en) 2006-04-06
TWI382973B (zh) 2013-01-21
AU2005289099B2 (en) 2012-07-19
JP2013067625A (ja) 2013-04-18
HN2005000768A (es) 2010-09-17
CA2581835C (en) 2012-12-18

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