MX353203B - Metodo para producir un derivado heterociclico fenilo sustituido por medio del metodo de acoplamiento utilizando un compuesto paladio. - Google Patents

Metodo para producir un derivado heterociclico fenilo sustituido por medio del metodo de acoplamiento utilizando un compuesto paladio.

Info

Publication number
MX353203B
MX353203B MX2013001768A MX2013001768A MX353203B MX 353203 B MX353203 B MX 353203B MX 2013001768 A MX2013001768 A MX 2013001768A MX 2013001768 A MX2013001768 A MX 2013001768A MX 353203 B MX353203 B MX 353203B
Authority
MX
Mexico
Prior art keywords
palladium compound
substituted heterocyclic
heterocyclic derivative
formula
producing phenyl
Prior art date
Application number
MX2013001768A
Other languages
English (en)
Other versions
MX2013001768A (es
Inventor
Komiyama Masato
Original Assignee
Teijin Pharma Ltd
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 Teijin Pharma Ltd filed Critical Teijin Pharma Ltd
Publication of MX2013001768A publication Critical patent/MX2013001768A/es
Publication of MX353203B publication Critical patent/MX353203B/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/06Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/4261,3-Thiazoles
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D277/56Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Pain & Pain Management (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

La presente invención proporciona un método para producir un inhibidor de xantina oxidasa, que es un agente terapéutico para la hiperuricemia, o intermediarios del mismo, el método que es eficiente y que utiliza un procedimiento corto. La presente invención es un método de acoplamiento novedoso para obtener un compuesto representado por la fórmula (3) provocando una reacción de acoplamiento entre un compuesto representado por la fórmula (1) y un compuesto representado por la fórmula (2), en la presencia de un compuesto de paladio, un ligando obtenido por la coordinación en un compuesto de paladio, una base, un ácido carboxílico de C1-C40, y por lo menos una clase de aditivo.
MX2013001768A 2010-08-27 2011-08-26 Metodo para producir un derivado heterociclico fenilo sustituido por medio del metodo de acoplamiento utilizando un compuesto paladio. MX353203B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2010190760 2010-08-27
PCT/JP2011/069250 WO2012026565A1 (ja) 2010-08-27 2011-08-26 パラジウム化合物を用いたカップリング法によるフェニル置換複素環誘導体の製造法

Publications (2)

Publication Number Publication Date
MX2013001768A MX2013001768A (es) 2013-03-22
MX353203B true MX353203B (es) 2018-01-05

Family

ID=45723554

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2013001768A MX353203B (es) 2010-08-27 2011-08-26 Metodo para producir un derivado heterociclico fenilo sustituido por medio del metodo de acoplamiento utilizando un compuesto paladio.

Country Status (20)

Country Link
US (1) US8916714B2 (es)
EP (1) EP2610248B1 (es)
JP (1) JP5654601B2 (es)
KR (1) KR101800054B1 (es)
CN (1) CN103068807B (es)
AU (1) AU2011294204B2 (es)
BR (1) BR112013003992B1 (es)
CA (1) CA2807543C (es)
DK (1) DK2610248T3 (es)
ES (1) ES2589977T3 (es)
HK (1) HK1179960A1 (es)
HU (1) HUE030166T2 (es)
IL (1) IL224923A (es)
MX (1) MX353203B (es)
PL (1) PL2610248T3 (es)
PT (1) PT2610248T (es)
RU (1) RU2563459C2 (es)
SG (1) SG187843A1 (es)
TW (1) TWI554505B (es)
WO (1) WO2012026565A1 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5312570B2 (ja) 2009-02-27 2013-10-09 帝人ファーマ株式会社 遷移金属触媒を用いたカップリング法によるフェニル置換複素環誘導体の製造法
RU2016148736A (ru) * 2014-05-13 2018-06-14 Тейдзин Фарма Лимитед Новые кристаллические полиморфы производного пиридина и способ их получения
CN110156698B (zh) * 2019-06-06 2020-10-13 沈阳海诺威医药科技有限公司 2-苯基-1,6-二氢嘧啶-5-甲酸衍生物的制备方法和用途
CN110683926B (zh) * 2019-09-29 2022-11-04 北京大学深圳研究生院 羧酸芳基酯类化合物的制备方法
CN110698431B (zh) * 2019-11-20 2022-07-01 陕西师范大学 一种1,2-苯并噻嗪类化合物的合成方法
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 (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4346094A (en) 1980-09-22 1982-08-24 Eli Lilly And Company 3-Aryl-5-isothiazolecarboxylic acids and related compounds used to lower uric acid levels
US4495195A (en) 1982-11-01 1985-01-22 Eli Lilly And Company Xanthine oxidase inhibiting 3(5)-phenyl-substituted-5(3)-pyrazole-carboxylic acid derivatives, compositions, and methods of use
DE122008000051I1 (de) 1990-11-30 2009-02-05 Teijin Ltd 2-arylthiazolderivat sowie dieses enthaltendes arzneimittel
JP3399559B2 (ja) 1992-08-12 2003-04-21 帝人株式会社 2−フェニル複素環式化合物
JP3113110B2 (ja) 1993-01-19 2000-11-27 帝人株式会社 イソキサゾールおよびイソチアゾール誘導体
JP3169735B2 (ja) 1993-04-08 2001-05-28 帝人株式会社 (アルコキシシアノフェニル)チアゾール誘導体の製造方法
JP2706037B2 (ja) 1993-04-13 1998-01-28 帝人株式会社 シアノ化合物およびその製造方法
JP2834971B2 (ja) 1993-05-25 1998-12-14 帝人株式会社 2−(4−アルコキシ−3−シアノフェニル)チアゾール誘導体の製造法およびその新規製造中間体
ID21775A (id) 1996-10-25 1999-07-22 Yoshitomi Pharmaceutical Senyawa-senyawa 1-fenilpirazol dan penggunaan farmasinya
JPH10139770A (ja) 1996-11-08 1998-05-26 Teijin Ltd 2−(3−シアノフェニル)チアゾール誘導体の製造法
JPH10310578A (ja) 1996-11-13 1998-11-24 Yoshitomi Pharmaceut Ind Ltd 3−フェニルピラゾール化合物
JP3440196B2 (ja) 1997-08-13 2003-08-25 帝人株式会社 チオベンズアミド誘導体の製造方法
JP2003523388A (ja) 2000-02-23 2003-08-05 アルテオン インコーポレーテッド チアゾリウム化合物及びタンパク質老化に関連する障害の治療
WO2002051849A1 (fr) 2000-12-26 2002-07-04 Daiichi Pharmaceutical Co., Ltd. Inhibiteurs cdk4
WO2004069394A2 (en) 2003-02-03 2004-08-19 The Trustees Of Columbia University In The City Of New York Synthetic method for direct arylation of heterocyclic arenes
MXPA05008450A (es) * 2003-02-10 2005-10-18 Vertex Pharma Procesos para la preparacion de n-heteroaril-n-aril-aminas mediante reaccion de un ester de acido n-aril-carbamico con un halo-heteroarilo y procesos analogos.
RU2006111093A (ru) 2003-09-06 2007-10-27 Вертекс Фармасьютикалз Инкорпорейтед (Us) Модуляторы атр-связывающих кассетных транспортеров
BRPI0507278A (pt) 2004-01-30 2007-06-26 Vertex Pharma moduladores dos transportadores do cassete de ligação ao atp
GB0402262D0 (en) * 2004-02-02 2004-03-10 Novartis Ag Process for the manufacture of organic compounds
EP1992361B1 (en) 2006-02-24 2012-05-02 Astellas Pharma Inc. Remedy or preventive for digestive ulcer
JP5312570B2 (ja) * 2009-02-27 2013-10-09 帝人ファーマ株式会社 遷移金属触媒を用いたカップリング法によるフェニル置換複素環誘導体の製造法

Also Published As

Publication number Publication date
AU2011294204B2 (en) 2015-07-23
ES2589977T3 (es) 2016-11-17
US8916714B2 (en) 2014-12-23
DK2610248T3 (en) 2016-07-25
MX2013001768A (es) 2013-03-22
US20130158272A1 (en) 2013-06-20
CN103068807B (zh) 2016-05-25
CA2807543C (en) 2018-08-28
PT2610248T (pt) 2016-08-23
EP2610248B1 (en) 2016-06-08
IL224923A (en) 2017-07-31
EP2610248A4 (en) 2013-10-16
KR101800054B1 (ko) 2017-11-21
TW201305122A (zh) 2013-02-01
AU2011294204A1 (en) 2013-03-21
HUE030166T2 (en) 2017-05-29
BR112013003992B1 (pt) 2021-07-20
CN103068807A (zh) 2013-04-24
PL2610248T3 (pl) 2016-12-30
RU2563459C2 (ru) 2015-09-20
JPWO2012026565A1 (ja) 2013-10-28
WO2012026565A1 (ja) 2012-03-01
EP2610248A1 (en) 2013-07-03
RU2013113576A (ru) 2014-10-10
HK1179960A1 (zh) 2013-10-11
KR20130138219A (ko) 2013-12-18
SG187843A1 (en) 2013-03-28
JP5654601B2 (ja) 2015-01-14
CA2807543A1 (en) 2012-03-01
BR112013003992A2 (pt) 2016-07-12
TWI554505B (zh) 2016-10-21

Similar Documents

Publication Publication Date Title
MX353203B (es) Metodo para producir un derivado heterociclico fenilo sustituido por medio del metodo de acoplamiento utilizando un compuesto paladio.
GEP20125537B (en) Derivatives of 1-phenyl-2-pyridinyl alkyl alcohols as phosphodiesterase inhibitors
NZ603268A (en) Process for synthesizing oxidized lactam compounds
MX2012002752A (es) Compuestos de heteroarilo como inhibidores de cinasa.
NZ612635A (en) Processes for producing cycloalkylcarboxamido-pyridine benzoic acids
MX2012005358A (es) Procedimiento para la preparacion de etexilato de dabigatran.
TNSN07325A1 (en) Pgd2 receptor antagonists for the treatment of inflammatory diseases
WO2009127338A8 (de) Oxo-heterocyclisch substituierte carbonsäure-derivate und ihre verwendung
MX2012003183A (es) Proceso para preparar metil ester de acido 3-[(4s)-8-bromo-1-metil -6-(2-piridinil) -4h-imidazo [1, 2-a] [1, 4] benzodiacepina-4-il] -propionico o la sal de sulfonato de benceno del mismo, y compuestos utiles en ese proceso.
MX341446B (es) Compuestos heterociclicos fusionados como inhibidores de fosfodiesterasas (pdes).
IN2012DN01273A (es)
NZ593172A (en) 4-azetidinyl-1-heteroaryl-cyclohexanol antagonists of ccr2
MX2011011776A (es) Nuevos profarmacos de triptolite.
MY150280A (en) Process of preparing derivatives of 1-(2-halobiphenyl-4-yl)-cyclopropanecarboxylic acid
MX2012002761A (es) Bipiridinas utiles para el tratamiento de enfermedades proliferativas.
PH12016502534A1 (en) Azaquinazoline carboxamide derivatives
MX2011008348A (es) Proceso para producir derivado heterociclico sustituido con fenilo a traves de acoplamiento usando catalizador de metal de transicion.
MX2011009898A (es) Proceso para la obtencion de derivados de acido propionico.
WO2010004578A3 (en) Novel and improved processes for the preparation of paliperidone
MX363730B (es) Procedimiento para la preparacion de derivados de acido antranilico sustituidos.
EA201390336A1 (ru) Способ получения промежуточного соединения для синтеза лекарственного средства
MX2008012488A (es) Un proceso de acoplamiento para preparar intermedios de quinolona.
MX2012006524A (es) Proceso para la sintesis de compuestos intermedios de utilidad para preparar compuestos sustituidos de indazol y azaindol.
NZ593763A (en) Method of preparing (+)-1,4-dihydro-7-[(3s,4s)-3methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid
MX2009004982A (es) Derivados heterociclicos como inhibidores cetp.

Legal Events

Date Code Title Description
FG Grant or registration