[go: up one dir, main page]

CO5670370A2 - Proceso para la preparacion de derivados de tetrazol a partir de azidas de organo-boro y de organo-aluminio - Google Patents

Proceso para la preparacion de derivados de tetrazol a partir de azidas de organo-boro y de organo-aluminio

Info

Publication number
CO5670370A2
CO5670370A2 CO06014919A CO06014919A CO5670370A2 CO 5670370 A2 CO5670370 A2 CO 5670370A2 CO 06014919 A CO06014919 A CO 06014919A CO 06014919 A CO06014919 A CO 06014919A CO 5670370 A2 CO5670370 A2 CO 5670370A2
Authority
CO
Colombia
Prior art keywords
residue
organo
formula
azidas
aluminio
Prior art date
Application number
CO06014919A
Other languages
English (en)
Inventor
Gottfried Sedelmeier
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
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of CO5670370A2 publication Critical patent/CO5670370A2/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D257/00Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04Five-membered rings
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/06Aluminium compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/06Aluminium compounds
    • C07F5/061Aluminium compounds with C-aluminium linkage
    • C07F5/066Aluminium compounds with C-aluminium linkage compounds with Al linked to an element other than Al, C, H or halogen (this includes Al-cyanide linkage)

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Toxicology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1.- Un proceso para la fabricación de un tetrazol de la Fórmula:o un tautómero o una sal del mismo, en donde R representa un residuo orgánico;el cual comprende: (i) hacer reaccionar un compuesto de la fórmula R-CN (lIa) con una azida de la fórmula (R1)(R2)M-N3 (lIb), en donde R tiene el significado definido anteriormente; R1 y R2, independientemente uno del otro, representan un residuo orgánico, tal como un residuo alifático, un residuo alicíclico, un residuo heteroalicíclico; un residuo alicíclico-alifático; un residuo heteroalicíclico-alifático; un residuo aromático carbocíclico o heterocíclico;un residuo aralifático, o un residuo heteroaralifático, estando cada residuo, independientemente uno del otro, insustituido o sustituido; y M es boro o aluminio; y (ii) aislar el compuesto resultante de la Fórmula (I).
CO06014919A 2003-07-15 2006-02-15 Proceso para la preparacion de derivados de tetrazol a partir de azidas de organo-boro y de organo-aluminio CO5670370A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0316546.1A GB0316546D0 (en) 2003-07-15 2003-07-15 Process for the manufacture of organic compounds

Publications (1)

Publication Number Publication Date
CO5670370A2 true CO5670370A2 (es) 2006-08-31

Family

ID=27763861

Family Applications (1)

Application Number Title Priority Date Filing Date
CO06014919A CO5670370A2 (es) 2003-07-15 2006-02-15 Proceso para la preparacion de derivados de tetrazol a partir de azidas de organo-boro y de organo-aluminio

Country Status (34)

Country Link
US (3) US7943647B2 (es)
EP (2) EP2116548A1 (es)
JP (2) JP5052132B2 (es)
KR (5) KR20130140915A (es)
CN (1) CN100475823C (es)
AR (1) AR045995A1 (es)
AT (1) ATE450541T1 (es)
AU (1) AU2004263265C1 (es)
BR (1) BRPI0412558A (es)
CA (1) CA2532175A1 (es)
CO (1) CO5670370A2 (es)
CY (1) CY1109809T1 (es)
DE (1) DE602004024402D1 (es)
DK (1) DK1646636T3 (es)
EC (2) ECSP066282A (es)
ES (1) ES2336333T3 (es)
GB (1) GB0316546D0 (es)
HR (1) HRP20100088T1 (es)
IL (2) IL172946A (es)
IS (1) IS8303A (es)
MA (1) MA27906A1 (es)
MX (1) MXPA06000561A (es)
MY (1) MY176840A (es)
NO (1) NO20060729L (es)
NZ (1) NZ544644A (es)
PE (2) PE20091786A1 (es)
PL (1) PL1646636T3 (es)
PT (1) PT1646636E (es)
RU (2) RU2006104322A (es)
SI (1) SI1646636T1 (es)
TN (1) TNSN06008A1 (es)
TW (2) TWI372754B (es)
WO (1) WO2005014602A1 (es)
ZA (1) ZA200600312B (es)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0316546D0 (en) * 2003-07-15 2003-08-20 Novartis Ag Process for the manufacture of organic compounds
JP4537678B2 (ja) * 2003-09-04 2010-09-01 住友化学株式会社 2’−(1h−テトラゾール−5−イル)ビフェニル−4−カルボアルデヒド結晶およびその製造方法
EP1661891A1 (en) * 2004-11-30 2006-05-31 KRKA, D.D., Novo Mesto A process for the synthesis of valsartan
GB0514206D0 (en) * 2005-07-11 2005-08-17 Novartis Ag Organic compounds
GB0514686D0 (en) * 2005-07-18 2005-08-24 Novartis Ag Organic compounds
KR101250820B1 (ko) * 2005-08-16 2013-04-04 수벤 라이프 사이언시스 리미티드 개선된 로사르탄 제조 방법
US7915425B2 (en) 2005-08-31 2011-03-29 Suven Life Sciences Limited Process for the preparation of losartan
KR100795589B1 (ko) * 2006-05-29 2008-01-21 주식회사 대희화학 2-부틸-4-클로로-1-[[2'-(1h-테트라졸-5-일)바이페닐-4-일]메틸]이미다졸-5-카르복스알데하이드의 제조방법
CN101200455B (zh) * 2007-09-29 2010-08-18 泰兴市江神化工有限公司 沙坦类治疗高血压药物主环5-(4'-甲酰基联苯-2-基)-1h-四氮唑的制备方法
EP2217580B1 (en) 2007-10-12 2011-12-21 ArQule, Inc. Substituted tetrazole compounds and uses thereof
EP2316821A1 (en) * 2009-10-27 2011-05-04 Novartis AG Process for the manufacture of organic compounds
JPWO2011061996A1 (ja) * 2009-11-17 2013-04-04 田辺三菱製薬株式会社 ビフェニル誘導体の製法
US10368340B2 (en) * 2010-04-01 2019-07-30 Hon Hai Precision Industry Co., Ltd. Network service exposure method and apparatus utilizing the same
KR101942064B1 (ko) * 2011-04-25 2019-01-24 주식회사 엘지화학 신규한 아연 아지드 착물 및 이를 이용한 테트라졸 유도체의 제조방법
CN102351804B (zh) * 2011-09-30 2013-07-31 浙江新赛科药业有限公司 一种缬沙坦消旋体的回收方法
CN102702117B (zh) * 2012-06-01 2016-04-13 浙江沙星医药化工有限公司 一种制备5-(4’-溴代甲基-2-联苯基)-1-三苯甲基四氮唑的方法
CN103265560B (zh) * 2013-05-17 2016-05-04 中国科学院上海高等研究院 棉酚/棉酮衍生物及其制备方法和抗肿瘤药物中的应用
KR101956281B1 (ko) * 2013-08-13 2019-03-08 삼성전기주식회사 수지 조성물, 이를 이용한 인쇄회로기판 및 그 제조방법
KR102090155B1 (ko) * 2019-11-22 2020-03-17 국방과학연구소 베타인 수용액 내에서 5-치환-1h-테트라졸의 제조방법
US11655220B2 (en) 2020-10-22 2023-05-23 Hetero Labs Limited Process for the preparation of angiotensin II receptor blockers
CN116375687A (zh) * 2021-12-22 2023-07-04 浙江华海药业股份有限公司 一种高纯度的氯沙坦钾及其制备方法

Family Cites Families (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2977372A (en) 1958-04-09 1961-03-28 William G Finnegan Process for preparing substituted tetrazoles
US3394142A (en) 1966-01-19 1968-07-23 Minnesota Mining & Mfg Substituted tetrazoles and process therefor
CH499526A (de) 1968-06-06 1970-11-30 Ciba Geigy Ag Verfahren zur Herstellung von neuen Tetrazolderivaten
SU497775A3 (ru) 1970-01-16 1975-12-30 Циба-Гейги Аг (Фирма) Способ получени производных тетразола
DE2650231A1 (de) 1976-11-02 1978-05-11 Hoechst Ag Neue imidazolverbindungen, verfahren zu ihrer herstellung und diese enthaltende arzneimittel
US4097479A (en) 1977-03-11 1978-06-27 Miles Laboratories, Inc. Synthesis of 5-substituted tetrazoles
US4122274A (en) 1977-05-25 1978-10-24 Bristol-Myers Company 3-Tetrazolo-5,6,7,8-substituted-pyrido[1,2-a]pyrimidin-4-ones
US4288352A (en) 1979-03-26 1981-09-08 Exxon Research & Engineering Co. Electrically conductive polymeric compositions
FI73423C (fi) * 1980-02-29 1987-10-09 Otsuka Pharma Co Ltd Foerfarande foer framstaellning av farmakologiskt verksamma tetrazolderivat.
JPS56158781A (en) 1980-05-10 1981-12-07 Kaken Pharmaceut Co Ltd Tetrazolecoumarin derivative, its preparation and antiallergic agent containing the same as active constitutent
US4338452A (en) * 1980-09-17 1982-07-06 Eli Lilly And Company 1-and 2-(1-Alkyl-1H-tetrazol-5-yl-methyl)-1H-tetrazol-5-thiols and 1-cyanomethyl tetrazole-5-thiol
US4735948A (en) 1983-03-25 1988-04-05 Merrell Dow Pharmaceuticals Inc. (1H-tetrazol-5-yl)-2(1H)-quinolinones and-naphthyridones and antiallergic use thereof
JPS6073028A (ja) 1983-09-29 1985-04-25 Japan Electronic Control Syst Co Ltd 電子制御燃料噴射式内燃機関の始動時の噴射量の学習制御装置
US5138069A (en) 1986-07-11 1992-08-11 E. I. Du Pont De Nemours And Company Angiotensin II receptor blocking imidazoles
CA1334092C (en) 1986-07-11 1995-01-24 David John Carini Angiotensin ii receptor blocking imidazoles
GB8708459D0 (en) 1987-04-09 1987-05-13 Avdel Ltd Fastener installation apparatus
US4870186A (en) 1987-05-22 1989-09-26 E. I. Du Pont De Nemours And Company Tetrazole intermediates to antihypertensive compounds
US4874867A (en) 1987-05-22 1989-10-17 E. I. Du Pont De Nemours And Company Tetrazole intermediates to antihypertensive compounds
US4820843A (en) 1987-05-22 1989-04-11 E. I. Du Pont De Nemours And Company Tetrazole intermediates to antihypertensive compounds
US4831192A (en) 1987-12-31 1989-05-16 Boc, Inc. Methods of preparing 4-heteropentacyclic-4-(N-phenyl)amido) piperidine derivatives and intermediate compounds
US5210079A (en) 1988-01-07 1993-05-11 E. I. Du Pont De Nemours And Company Treatment of chronic renal failure with imidazole angiotensin-II receptor antagonists
US5128069A (en) * 1989-03-22 1992-07-07 Nippon Zoki Pharmaceutical Co., Ltd. Luciferin derivatives
IL97219A (en) * 1990-02-19 1995-12-08 Ciba Geigy Ag Biphenyl substituted aliphatic amino compounds process for their preparation and pharmaceutical compositions containing them
US5270317A (en) 1990-03-20 1993-12-14 Elf Sanofi N-substituted heterocyclic derivatives, their preparation and the pharmaceutical compositions in which they are present
PT97078B (pt) 1990-03-20 1997-07-31 Sanofi Sa Processo para a preparacao de derivados heterociclicos n-substituidos e de composicoes farmaceuticas que os contem
US5196444A (en) 1990-04-27 1993-03-23 Takeda Chemical Industries, Ltd. 1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate and compositions and methods of pharmaceutical use thereof
JPH04297466A (ja) 1990-06-22 1992-10-21 Nippon Shinyaku Co Ltd テトラゾール誘導体及び医薬
US5284954A (en) 1990-09-10 1994-02-08 Abbott Laboratories Process for the preparation of tetrazoles
WO1992010189A1 (en) 1990-12-14 1992-06-25 Smithkline Beecham Corporation Imidazolyl-alkenoic acids
SI9210098B (sl) 1991-02-06 2000-06-30 Dr. Karl Thomae Benzimidazoli, zdravila, ki te spojine vsebujejo, in postopek za njihovo pripravo
US5614519A (en) 1991-02-06 1997-03-25 Karl Thomae Gmbh (1-(2,3 or 4-N-morpholinoalkyl)-imidazol-4-yl)-benizimidazol-1-yl-methyl]-biphenyls useful as angiotensin-II antagonists
US5602127A (en) 1991-02-06 1997-02-11 Karl Thomae Gmbh (Alkanesultam-1-yl)-benzimidazol-1-yl)-1yl)-methyl-biphenyls useful as angiotensin-II antagonists
US5594003A (en) 1991-02-06 1997-01-14 Dr. Karl Thomae Gmbh Tetrahydroimidazo[1,2-a]pyridin-2-yl-(benzimidazol-1-yl)-methyl-biphenyls useful as angiotensin-II antagonists
CA2229000C (en) 1991-02-21 2002-04-09 Sankyo Company, Limited 1-biphenylimidazole derivatives, their preparation and their therapeutic use
JP2524842Y2 (ja) 1991-02-28 1997-02-05 三菱重工業株式会社 原紙供給装置
US5447949A (en) 1991-05-15 1995-09-05 Smithkline Beecham Corporation N-(heteroaryl) imidazolyl-alkenoic acids having angiotension II receptor antagonist activity
CA2115990A1 (en) 1991-08-19 1993-03-04 George Albert Boswell Angiotensin ii receptor blocking imidazolinone derivatives
AU657790B2 (en) 1991-08-22 1995-03-23 Warner-Lambert Company Amide tetrazole ACAT inhibitors
EP0550313A1 (fr) 1991-12-30 1993-07-07 Synthelabo Nouveaux dérivés de 2-(tétrazol-5-yl)-(1,1'-biphényle), leur préparation et leur utilisation comme intermédiaires de synthèse
IL104406A0 (en) 1992-01-17 1993-05-13 Syntex Inc Substituted 1-isoquinolone derivatives,their preparation and pharmaceutical compositions containing them
DE4203872A1 (de) * 1992-02-11 1993-08-12 Thomae Gmbh Dr K Imidazo(1,2-a)pyridine, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung
DE4206045A1 (de) 1992-02-27 1993-09-02 Bayer Ag Sulfonylbenzyl substituierte pyridone
US5484955A (en) 1992-07-06 1996-01-16 Takeda Chemical Industries, Ltd. Tri-higher alkyl tin azide and its use
JP2990566B2 (ja) * 1992-07-06 1999-12-13 武田薬品工業株式会社 トリ高級アルキルスズアジドおよびその用途
JPH06107658A (ja) 1992-09-28 1994-04-19 Kanebo Ltd 新規なピラジン誘導体
US5256658A (en) 1993-01-15 1993-10-26 Ortho Pharmaceutical Corporation Angiotensin II inhibitors
US5502191A (en) 1993-07-01 1996-03-26 American Cyanamid Company Method of synthesizing sterically hindered 5-substituted-1H-tetrazoles from nitriles using a lewis acid and an azide
EP0736021A4 (en) 1993-12-23 1997-04-02 Merck & Co Inc LOSARTAN POLYMORPH AND METHOD FOR PRODUCING FORM II LOSARTAN
NZ281496A (en) 1994-03-25 1998-02-26 Merrell Pharma Inc Preparation of (1h-tetrazol-5-yl)tetrazolo[1,5-a]quinolines and -naphthyridines
DK0752990T3 (da) 1994-03-28 1999-02-08 Pfizer Benzisothiazolderivater som inhibitorer af 5-lipoxygenasebiosyntese
US5541209A (en) 1994-08-22 1996-07-30 Bristol-Myers Squibb Company Method of treating or preventing cardiac arrhythmia employing an N-substituted heterocyclic derivative
JPH08325248A (ja) 1995-05-26 1996-12-10 Chugoku Kayaku Kk テトラゾール類の新規な合成試薬及びそれを用いたテトラゾール類の製造方法
JP3671266B2 (ja) 1996-03-21 2005-07-13 東洋化成工業株式会社 5−置換テトラゾール類の製造方法
JPH10218868A (ja) 1997-02-12 1998-08-18 Toyo Kasei Kogyo Co Ltd 5ーメチルテトラゾールの製造方法
JP4450881B2 (ja) 1998-12-28 2010-04-14 株式会社日本ファインケム 5,5’−ビ−1h−テトラゾール塩の製造方法
JP2000281662A (ja) 1999-03-31 2000-10-10 Masuda Kagaku Kogyo Kk テトラゾール類の製造方法
DE19935219A1 (de) * 1999-07-27 2001-02-01 Boehringer Ingelheim Pharma Carbonsäureamide, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Herstellung
DE60025831T2 (de) * 1999-09-27 2006-08-10 Dow Global Technologies, Inc., Midland Expandierte anionen enthaltende geträgertes katalysatorsystem
US20040072886A1 (en) * 2002-04-15 2004-04-15 Dr. Reddy's Laboratories Limited Novel crystalline forms of (S)-N- (1-Carboxy-2-methyl-prop-1-yl) -N-pentanoyl-N- [2' -(1H-tetrazol-5-yl)- biphenyl-4-yl methyl] amine (Valsartan)
GB0222056D0 (en) 2002-09-23 2002-10-30 Novartis Ag Process for the manufacture of organic compounds
US6934312B2 (en) * 2002-09-30 2005-08-23 Agilent Technologies, Inc. System and method for fabricating efficient semiconductor lasers via use of precursors having a direct bond between a group III atom and a nitrogen atom
GB0316546D0 (en) * 2003-07-15 2003-08-20 Novartis Ag Process for the manufacture of organic compounds
ATE380183T1 (de) * 2003-08-08 2007-12-15 Dipharma Francis Srl Verfahren zur herstellung von phenyltetrazolderivaten
BRPI0508164A (pt) 2004-03-17 2007-08-07 Kennecott Utah Copper Corp aparelho e método para monitorar uma célular eletrolìtica

Also Published As

Publication number Publication date
IL172946A (en) 2012-01-31
JP2011184451A (ja) 2011-09-22
TWI340742B (en) 2011-04-21
BRPI0412558A (pt) 2006-09-19
PE20091786A1 (es) 2009-12-14
KR20110082096A (ko) 2011-07-15
AU2004263265B2 (en) 2007-09-06
JP2009513555A (ja) 2009-04-02
HRP20100088T1 (hr) 2010-06-30
NO20060729L (no) 2006-04-04
PL1646636T3 (pl) 2010-05-31
TWI372754B (en) 2012-09-21
MXPA06000561A (es) 2006-03-30
PT1646636E (pt) 2010-01-29
TNSN06008A1 (en) 2007-10-03
IS8303A (is) 2006-02-14
CY1109809T1 (el) 2014-09-10
PE20050710A1 (es) 2005-09-28
EP1646636A1 (en) 2006-04-19
DE602004024402D1 (de) 2010-01-14
JP5052132B2 (ja) 2012-10-17
AU2004263265C1 (en) 2008-09-25
KR20120018826A (ko) 2012-03-05
ECSP066282A (es) 2006-07-28
IL216449A0 (en) 2011-12-29
TW200510347A (en) 2005-03-16
EP1646636B1 (en) 2009-12-02
ES2336333T3 (es) 2010-04-12
KR20130127011A (ko) 2013-11-21
DK1646636T3 (da) 2010-04-06
MY176840A (en) 2020-08-24
IL172946A0 (en) 2006-06-11
US20070043098A1 (en) 2007-02-22
US7943647B2 (en) 2011-05-17
ATE450541T1 (de) 2009-12-15
WO2005014602A1 (en) 2005-02-17
EP2116548A1 (en) 2009-11-11
MA27906A1 (fr) 2006-05-02
RU2006104322A (ru) 2007-09-20
CN100475823C (zh) 2009-04-08
KR20060038994A (ko) 2006-05-04
KR101336435B1 (ko) 2013-12-04
CN1852908A (zh) 2006-10-25
AU2004263265A1 (en) 2005-02-17
ZA200600312B (en) 2007-02-28
GB0316546D0 (en) 2003-08-20
KR20130140915A (ko) 2013-12-24
SI1646636T1 (sl) 2010-03-31
ECSP11006282A (es) 2011-08-31
CA2532175A1 (en) 2005-02-17
TW201038540A (en) 2010-11-01
US20120330026A1 (en) 2012-12-27
US8569528B2 (en) 2013-10-29
US20110184187A1 (en) 2011-07-28
HK1093509A1 (en) 2007-03-02
RU2012149012A (ru) 2014-05-27
AR045995A1 (es) 2005-11-23
NZ544644A (en) 2008-07-31

Similar Documents

Publication Publication Date Title
CO5670370A2 (es) Proceso para la preparacion de derivados de tetrazol a partir de azidas de organo-boro y de organo-aluminio
ECSP055974A (es) Síntesis de cloruros de 4 amino-2-butenoil y su uso en la preparación de 3-ciano quinolinas
UA93883C2 (ru) Производные пиразина, полезные kak антагонисты аденозинового рецептора
AR061058A1 (es) Derivados de piridopirimidininona. procesos de obtencion y composiciones farmaceuticas
AR052419A1 (es) Derivados de bencimidazolil n-sustituidos,inhibidores del protooncogen c-kit
PE20071322A1 (es) Derivados de 2-morfolinopirimidina como inhibidores de fosfatidinoinositol(pi) 3-quinasa
PE20060873A1 (es) Compuestos de quinolina heteroaromaticos
PE20090897A1 (es) Compuestos de biciclolactama sustituida como inhibidores de la enzima dgat-1
AR054809A1 (es) Compuestos de amino -5-heteroarilo (5 miembros) imidazolona y su uso para la modulacion de la b- secretasa
CO6160312A2 (es) Derivados de quiniclidina de acido (hetero) arilcicloheptano carboxilico como antagonistas del receptor muscarinico
TW200611907A (en) Fused heterocyclic compound
AR077695A1 (es) Derivados de pirimidina como inhibidores del factor ixa
AR044519A1 (es) Derivados de piridin-tiazol amina y de pirimidin-tiazol amina
AR054088A1 (es) Triazoles como inhibidores de proteinquinasas. composiciones farmaceuticas
AR042602A1 (es) Compuestos de 1,2,4-triazol
PE20040934A1 (es) Derivados de pirimidina como inhibidores selectivos de tirosina quinasas
PE20040808A1 (es) Derivados de urea ciclica como inhibidores de quinasas
AR062258A1 (es) Compuestos heterociclicos condensados de tieno-pirrol, composiciones farmaceuticas que los contienen y usos para el tratamiento de infecciones por hcv
CO6160314A2 (es) Compuestos benzoil amino heterociclil como activadores de la glucoquinasa (glk)
AR065795A1 (es) Derivados de aza-piridopirimidinona,metodo de preparacion,medicamentos que los contienen y usos como agentes antitromboticos, antihiperlipidemicos y antidiabeticos,entre otros.
GB0412769D0 (en) Organic compounds
PE20070009A1 (es) Tigeciclina y metodos para su preparacion
AR064626A1 (es) Sintesis de compuestos de pirrolidina
BR112015001769A2 (pt) Processo para a síntese de compostos de ureia substituída
PE20120766A1 (es) Derivados de quinoxalina como inhibidores de tumores