AR064312A1 - Procedimientos para la preparacion de 3-(4-(2,4-difluorobenciloxi)-3-bromo-6-metil-2-oxopiridin-1(2h)-il)-n,4-dimetilbenzamida - Google Patents

Procedimientos para la preparacion de 3-(4-(2,4-difluorobenciloxi)-3-bromo-6-metil-2-oxopiridin-1(2h)-il)-n,4-dimetilbenzamida

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Publication number
AR064312A1
AR064312A1 ARP070105576A ARP070105576A AR064312A1 AR 064312 A1 AR064312 A1 AR 064312A1 AR P070105576 A ARP070105576 A AR P070105576A AR P070105576 A ARP070105576 A AR P070105576A AR 064312 A1 AR064312 A1 AR 064312A1
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AR
Argentina
Prior art keywords
compound
formula
contacting
alkyl
produce
Prior art date
Application number
ARP070105576A
Other languages
English (en)
Spanish (es)
Inventor
G Klemm
R Vanderroest
B Chekal
M Mao
Embse R Vonder
R Geurnik
G Yalamanchili
R Valdyanathan
D Dukeshereer
Original Assignee
Pfizer Prod 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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of AR064312A1 publication Critical patent/AR064312A1/es

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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
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/64One oxygen atom attached in position 2 or 6
    • 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
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

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  • Urology & Nephrology (AREA)
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ARP070105576A 2006-12-13 2007-12-12 Procedimientos para la preparacion de 3-(4-(2,4-difluorobenciloxi)-3-bromo-6-metil-2-oxopiridin-1(2h)-il)-n,4-dimetilbenzamida AR064312A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US86974806P 2006-12-13 2006-12-13

Publications (1)

Publication Number Publication Date
AR064312A1 true AR064312A1 (es) 2009-03-25

Family

ID=39365911

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP070105576A AR064312A1 (es) 2006-12-13 2007-12-12 Procedimientos para la preparacion de 3-(4-(2,4-difluorobenciloxi)-3-bromo-6-metil-2-oxopiridin-1(2h)-il)-n,4-dimetilbenzamida

Country Status (17)

Country Link
US (1) US7906536B2 (https=)
EP (1) EP2102161B1 (https=)
JP (1) JP2008231090A (https=)
KR (1) KR20090090379A (https=)
CN (1) CN101611006A (https=)
AR (1) AR064312A1 (https=)
AT (1) ATE556055T1 (https=)
AU (1) AU2007331199A1 (https=)
BR (1) BRPI0720757A2 (https=)
CA (1) CA2672256C (https=)
IL (1) IL199239A0 (https=)
MX (1) MX2009006266A (https=)
NZ (1) NZ577639A (https=)
RU (1) RU2411236C1 (https=)
TW (1) TW200837057A (https=)
WO (1) WO2008072079A2 (https=)
ZA (1) ZA200903981B (https=)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5679159B2 (ja) 2010-07-05 2015-03-04 信越化学工業株式会社 希土類金属抽出剤の合成方法、及び希土類金属の溶媒抽出用有機相
WO2014181213A1 (en) 2013-05-10 2014-11-13 Pfizer Inc. Crystalline form of (sa)-(-)-3-(3-bromo-4-((2,4-difluorobenzyl)oxy)-6-methyl-2-oxopyridin-1 (2h)-yl)-n,4-dimethylbenzamide
US10342786B2 (en) 2017-10-05 2019-07-09 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD
WO2019071147A1 (en) 2017-10-05 2019-04-11 Fulcrum Therapeutics, Inc. INHIBITORS OF KINASE P38 REDUCING EXPRESSION OF DUX4 GENE AND DOWNSTREAM GENES FOR THE TREATMENT OF FSHD
MX2022004631A (es) * 2019-10-18 2022-05-24 Fmc Corp Metodos para la preparacion del acido 5-bromo-2-(3-cloropiridin-2- il)-2h-pirazol-3-carboxilico.

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3286645B2 (ja) * 1993-03-26 2002-05-27 メルシャン株式会社 光学活性1,4−ジヒドロピリジン誘導体およびその製造方法
RS52392B (sr) * 2002-02-14 2013-02-28 Pharmacia Corporation Supstituisani piridinoni kao modulatori p38 map kinaze
CL2004002050A1 (es) * 2003-08-13 2005-06-03 Pharmacia Corp Sa Organizada B Compuestos derivados de piridinonas sustituidas; su uso en el tratamiento de afecciones causadas o exacerbadas por actividad p38 map kinasa y/o tnf no regulada, tales como inflamaciones, tumores, sida y otros.
WO2006021885A1 (en) * 2004-08-26 2006-03-02 Pfizer Inc. Enantioselective biotransformation for preparation of protein tyrosine kinase inhibitor intermediates
CA2640665A1 (en) * 2006-02-10 2007-08-16 Pfizer Products Inc. Pyridinone pyrazole urea and pyrimidinone pyrazole urea derivatives

Also Published As

Publication number Publication date
TW200837057A (en) 2008-09-16
BRPI0720757A2 (pt) 2014-01-14
RU2411236C1 (ru) 2011-02-10
WO2008072079A3 (en) 2008-08-07
ATE556055T1 (de) 2012-05-15
WO2008072079A2 (en) 2008-06-19
EP2102161B1 (en) 2012-05-02
ZA200903981B (en) 2010-08-25
US7906536B2 (en) 2011-03-15
CN101611006A (zh) 2009-12-23
IL199239A0 (en) 2010-03-28
MX2009006266A (es) 2009-06-22
AU2007331199A1 (en) 2008-06-19
CA2672256C (en) 2011-08-30
EP2102161A2 (en) 2009-09-23
NZ577639A (en) 2012-01-12
KR20090090379A (ko) 2009-08-25
CA2672256A1 (en) 2008-06-19
JP2008231090A (ja) 2008-10-02
US20080177077A1 (en) 2008-07-24

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