PE20091786A1 - Proceso para preparar tetrazoles antagonistas del receptor de angiotensina ii - Google Patents
Proceso para preparar tetrazoles antagonistas del receptor de angiotensina iiInfo
- Publication number
- PE20091786A1 PE20091786A1 PE2009001025A PE2009001025A PE20091786A1 PE 20091786 A1 PE20091786 A1 PE 20091786A1 PE 2009001025 A PE2009001025 A PE 2009001025A PE 2009001025 A PE2009001025 A PE 2009001025A PE 20091786 A1 PE20091786 A1 PE 20091786A1
- Authority
- PE
- Peru
- Prior art keywords
- tetrazoles
- receptor antagonists
- formula
- angiotensin
- ckyls
- Prior art date
Links
- 239000002333 angiotensin II receptor antagonist Substances 0.000 title abstract 2
- 150000003536 tetrazoles Chemical class 0.000 title abstract 2
- KJUGUADJHNHALS-UHFFFAOYSA-N 1H-tetrazole Substances C=1N=NNN=1 KJUGUADJHNHALS-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052782 aluminium Chemical group 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 229940126317 angiotensin II receptor antagonist Drugs 0.000 abstract 1
- 150000001540 azides Chemical class 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 229910052796 boron Inorganic materials 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic 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
- C07D403/10—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/061—Aluminium compounds with C-aluminium linkage
- C07F5/066—Aluminium 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)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (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
REFERIDA A UN PROCESO DE PREPARACION DE UN ANTAGONISTA DEL RECEPTOR DE ANGIOTENSINA II, EL CUAL ES UN DERIVADO DE TETRAZOL DE FORMULA (IVb), DONDE DICHO PROCESO CONSISTE EN HACER REACCIONAR UN COMPUESTO DE FORMULA (IVc) O UN ALQUILESTER C1-C7 O UN BENCILESTER DEL MISMO, CON UNA AZIDA DE FORMULA (R1)(R2)M-N3 PARA LUEGO AISLAR EL COMPUESTO (IVb), DONDE R1 Y R2 SON UN RESIDUO ALIFATICO TAL COMO ALQUILO C1-C20, ALQUENILO C3-C20, UN RESIDUO AROMATICO CARBOCICLICO TAL COMO FENILO, NAFTILO O BIFENILO, ENTRE OTROS Y M ES BORO O ALUMINIO
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 |
---|---|
PE20091786A1 true PE20091786A1 (es) | 2009-12-14 |
Family
ID=27763861
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2009001025A PE20091786A1 (es) | 2003-07-15 | 2004-07-14 | Proceso para preparar tetrazoles antagonistas del receptor de angiotensina ii |
PE2004000667A PE20050710A1 (es) | 2003-07-15 | 2004-07-14 | Proceso para la preparacion de derivados de tetrazoles utilizando azidas de organo boro y organo aluminio |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2004000667A PE20050710A1 (es) | 2003-07-15 | 2004-07-14 | Proceso para la preparacion de derivados de tetrazoles utilizando azidas de organo boro y organo aluminio |
Country Status (35)
Country | Link |
---|---|
US (3) | US7943647B2 (es) |
EP (2) | EP2116548A1 (es) |
JP (2) | JP5052132B2 (es) |
KR (5) | KR101336435B1 (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) |
HK (1) | HK1093509A1 (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)
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 |
WO2007020654A1 (en) * | 2005-08-16 | 2007-02-22 | Suven Life Sciences | An improved process for the preparation of losartan |
WO2007026375A1 (en) * | 2005-08-31 | 2007-03-08 | Suven Life Sciences | 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 |
WO2012148148A2 (en) * | 2011-04-25 | 2012-11-01 | Lg Life Sciences Ltd. | Novel zinc azide complex and a process for preparing tetrazole derivatives using the same |
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)
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 |
US4874867A (en) * | 1987-05-22 | 1989-10-17 | E. I. Du Pont De Nemours And Company | Tetrazole intermediates to antihypertensive compounds |
US4870186A (en) * | 1987-05-22 | 1989-09-26 | 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 |
ATE134624T1 (de) * | 1990-02-19 | 1996-03-15 | Ciba Geigy Ag | Acylverbindungen |
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 |
IE910913A1 (en) | 1990-03-20 | 1991-09-25 | Sanofi Sa | N-substituted heterocyclic derivates, their preparation¹and pharmaceutical compositions containing them |
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 |
AU9137791A (en) | 1990-12-14 | 1992-07-08 | Smithkline Beecham Corporation | Imidazolyl-alkenoic acids |
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 |
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 |
FI112942B3 (fi) | 1991-02-21 | 2012-03-13 | Daiichi Sankyo Co Ltd | Menetelmä kohonneen verenpaineen hoitoon ja ennaltaehkäisyyn käyttökelpoisten 4'-(1H-imidatsol-1-yylimetyyli)-1,1' -bifenyylijohdannaisten valmistamiseksi |
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 |
WO1993004046A1 (en) | 1991-08-19 | 1993-03-04 | E.I. Du Pont De Nemours And Company | Angiotensin ii receptor blocking imidazolinone derivatives |
WO1993004052A1 (en) | 1991-08-22 | 1993-03-04 | 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 |
ZA93282B (en) | 1992-01-17 | 1994-07-15 | Syntex Inc | Substituted 1-isoquinolone derivatives |
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 |
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 |
US5484955A (en) | 1992-07-06 | 1996-01-16 | Takeda Chemical Industries, Ltd. | Tri-higher alkyl tin azide and its use |
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 | LOSARTANE POLYMORPHS AND PROCESS FOR THE PREPARATION OF FORM II OF LOSARTANE |
DK0751945T3 (da) | 1994-03-25 | 1999-04-12 | Merrell Pharma Inc | Fremgangsmåde til fremstilling af (1H-tetrazol-5-yl)tetrazolo[1,5-A]quinoliner og -naphthyridiner |
CA2186513C (en) | 1994-03-28 | 1999-03-16 | James F. Eggler | Benzisothiazoles derivatives as inhibitors of 5-lipoxygenase biosynthesis |
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 |
ES2256025T3 (es) * | 1999-09-27 | 2006-07-16 | Dow Global Technologies Inc. | Catalizadores soportados sque comprenden aniones expandidos. |
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 |
PL1660463T3 (pl) * | 2003-08-08 | 2008-05-30 | Dipharma Francis Srl | Sposób wytwarzania pochodnych fenylotetrazolu |
AU2005224673B2 (en) | 2004-03-17 | 2010-03-04 | Kennecott Utah Copper Llc | Wireless electrolytic cell monitoring powered by ultra low bus voltage |
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