UA5557A1 - Спосіб отримання заміщенних похідних імідазолу - Google Patents

Спосіб отримання заміщенних похідних імідазолу

Info

Publication number
UA5557A1
UA5557A1 UA3463047A UA3463047A UA5557A1 UA 5557 A1 UA5557 A1 UA 5557A1 UA 3463047 A UA3463047 A UA 3463047A UA 3463047 A UA3463047 A UA 3463047A UA 5557 A1 UA5557 A1 UA 5557A1
Authority
UA
Ukraine
Prior art keywords
preparation
imidazole derivatives
substituted imidazole
hydrogenated
necessary
Prior art date
Application number
UA3463047A
Other languages
English (en)
Russian (ru)
Inventor
Карьялайнен Арто-Йоханнес
Ойва Антеро Куркела Кауко
Калерво Похьяла Еско
Original Assignee
Оріон Іхтюмя Ой
Орион Ихтюмя Ой
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 Оріон Іхтюмя Ой, Орион Ихтюмя Ой filed Critical Оріон Іхтюмя Ой
Publication of UA5557A1 publication Critical patent/UA5557A1/uk

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/63Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • 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
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10Antioedematous agents; Diuretics
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/69Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to carbon-to-carbon double or triple bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
    • C07C45/74Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups combined with dehydration
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/20Unsaturated compounds containing keto groups bound to acyclic carbon atoms
    • C07C49/213Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing six-membered aromatic rings
    • C07C49/217Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing six-membered aromatic rings having unsaturation outside the aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Catalysts (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Предметом винаходу є спосіб отримання заміщених похідних імідазолу. Він включає взаємодію з реактивом Гриньяра. Отримувана сполука піддається гідруванню або, якщо необхідно, вводиться в реакцію з КНSО4 і, якщо необхідно, піддається гідруванню продукт, що утворився.
UA3463047A 1981-07-10 1982-07-09 Спосіб отримання заміщенних похідних імідазолу UA5557A1 (uk)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB08121333A GB2101114B (en) 1981-07-10 1981-07-10 Substituted imidazole derivatives and their preparation and use

Publications (1)

Publication Number Publication Date
UA5557A1 true UA5557A1 (uk) 1994-12-28

Family

ID=10523160

Family Applications (1)

Application Number Title Priority Date Filing Date
UA3463047A UA5557A1 (uk) 1981-07-10 1982-07-09 Спосіб отримання заміщенних похідних імідазолу

Country Status (23)

Country Link
US (3) US4544664A (uk)
EP (1) EP0072615B1 (uk)
JP (1) JPS5818365A (uk)
KR (1) KR860001864B1 (uk)
AT (1) ATE17121T1 (uk)
AU (1) AU554125B2 (uk)
BG (1) BG60763B2 (uk)
CA (1) CA1184559A (uk)
DD (1) DD207713A1 (uk)
DE (1) DE3268111D1 (uk)
DK (2) DK158307C (uk)
FI (1) FI77858C (uk)
GB (1) GB2101114B (uk)
HK (1) HK8289A (uk)
HU (1) HU187773B (uk)
IE (1) IE53244B1 (uk)
IL (1) IL66271A (uk)
NO (1) NO160439C (uk)
NZ (1) NZ201176A (uk)
SG (1) SG65388G (uk)
SU (1) SU1241990A3 (uk)
UA (1) UA5557A1 (uk)
ZA (1) ZA824875B (uk)

Families Citing this family (70)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2069481B (en) * 1980-02-13 1983-07-27 Farmos Oy Substituted imidazole derivatives
GB2101114B (en) * 1981-07-10 1985-05-22 Farmos Group Ltd Substituted imidazole derivatives and their preparation and use
US4482723A (en) * 1983-04-11 1984-11-13 Pfizer Inc. Process for preparation of 4-acetyl-2-substituted-imidazoles
US4605661A (en) * 1984-06-18 1986-08-12 Eli Lilly And Company Aromastase inhibiting α,α-diarylimidazole-4(5)-propionitriles, α,α-diarylimidazole-4(5)-propionamides, and 4(5)-(2,2-diarylethyl)imidazoles
US4661508A (en) * 1984-06-18 1987-04-28 Eli Lilly And Company Aromatase inhibiting α,α-diphenyl-4(5)imidazole-methanes or -ethanes
ZA854400B (en) * 1984-06-18 1987-02-25 Lilly Co Eli 4(5)-substituted imidazoles
FI844786A0 (fi) * 1984-12-04 1984-12-04 Farmos Oy Terapeutiskt utnyttjbar foerening.
US4600683A (en) * 1985-04-22 1986-07-15 International Business Machines Corp. Cross-linked polyalkenyl phenol based photoresist compositions
GB8626287D0 (en) * 1986-11-04 1986-12-03 Ucb Sa Substituted 1h-imidazoles
FI864570A0 (fi) * 1986-11-11 1986-11-11 Farmos Oy Terapeutiskt anvaendbar foerening.
GB2206880B (en) * 1987-07-16 1991-04-24 Farmos Oy Optical isomers of an imidazole derivative
GB2210875B (en) * 1987-10-09 1991-05-29 Farmos Oy Aromatase inhibiting 4(5)-imidazoles
GB2215206B (en) 1988-02-29 1991-07-03 Farmos Oy 4-substituted imidazole derivatives useful in perioperative care
GB8810067D0 (en) 1988-04-28 1988-06-02 Ucb Sa Substituted 1-(1h-imidazol-4-yl)alkyl-benzamides
GB2229719B (en) * 1989-03-30 1992-04-29 Farmos Oy Novel aromatase inhibiting 4(5)-imidazoles
US5439928A (en) * 1989-03-30 1995-08-08 Orion-Yhtyma Oy Aromatase inhibiting 4(5)-imidazoles
US5124157A (en) 1989-08-18 1992-06-23 Cygnus Therapeutic Systems Method and device for administering dexmedetomidine transdermally
US5151526A (en) * 1990-10-11 1992-09-29 The United States Of America As Represented By The Secretary Of The Army 4-[1-(1-naphthalenyl)ethyl]-1H-imidazole, method of making and use as an anesthetic
DE4033042A1 (de) * 1990-10-18 1992-05-07 Joseph Heinz W Dr Verwendung von 4,5 - disubstituierten imidazolen zur herstellung von antimykotischen oder fungiziden mitteln
GB9111732D0 (en) * 1991-05-31 1991-07-24 Orion Yhtymae Oy The use of certain salts of medetomidine and its optically active enantiomers to regulate the rate of transdermal administration of the drugs
GB2256135B (en) * 1991-05-31 1995-01-18 Orion Yhtymae Oy Transdermal administration of 4-substituted imidazoles
US5401851A (en) * 1992-06-03 1995-03-28 Eli Lilly And Company Angiotensin II antagonists
SE9302333D0 (sv) * 1993-07-06 1993-07-06 Ab Astra New compounds
GB9521680D0 (en) * 1995-10-23 1996-01-03 Orion Yhtymo Oy New use of imidazole derivatives
UA64751C2 (uk) 1997-06-25 2004-03-15 Пфайзер Продактс Інк. Спосіб лікування інсулінової толерантності речовинами, які посилюють секрецію гормону росту (варіанти) та фармацевтична композиція (варіанти)
AR015744A1 (es) * 1998-04-01 2001-05-16 Orion Corp Uso de dexmedetomidina para sedacion en terapia intensiva
US6231594B1 (en) * 1999-08-11 2001-05-15 Radiant Medical, Inc. Method of controlling body temperature while reducing shivering
ATE321552T1 (de) * 1999-10-22 2006-04-15 Takeda Pharmaceutical 1-substituierte-phenyl-1-(1h-imidazol-4- yl)alkohole, verfahren zu deren herstellung sowie deren verwendung
US6582457B2 (en) * 2001-02-15 2003-06-24 Radiant Medical, Inc. Method of controlling body temperature while reducing shivering
MXPA05009290A (es) 2003-03-07 2006-05-31 Astellas Pharma Inc Derivados heterociclicos que contienen nitrogeno que tienen estirilo 2,6-disustituido.
AU2007209380B2 (en) * 2006-01-27 2011-12-08 F. Hoffmann-La Roche Ag Use of 4-imidazole derivatives for CNS disorders
EP1918282A1 (en) * 2006-11-06 2008-05-07 "Joint Stock Company Grindeks" Method for preparing medetomidine and its salts
US20080146523A1 (en) * 2006-12-18 2008-06-19 Guido Galley Imidazole derivatives
BRPI0812385A2 (pt) 2007-05-23 2019-09-24 Allergan Inc lactamas cíclicas para o tratamento de glaucoma ou pressão intraocular elevada
DK2160386T3 (da) 2007-05-23 2012-08-27 Allergan Inc Terapeutiske ((phenyl)imidazolyl)methylquinolinylforbindelser
GB2453982B (en) * 2007-10-24 2009-09-16 Norbrook Lab Ltd Chemical process for the preparation of Medetomidine
US7902247B2 (en) 2008-01-09 2011-03-08 Allergan, Inc. Substituted-aryl-2-phenylethyl-1H-imidazole compounds as subtype selective modulators of alpha 2B and/or alpha 2C adrenergic receptors
CA2712256A1 (en) 2008-01-18 2009-07-23 Allergan, Inc. Substitued-aryl-(imidazole)-methyl)-phenyl compounds as subtype selective modulators of alpha 2b and/or alpha 2c adrenergic receptors
US7795263B2 (en) * 2008-07-08 2010-09-14 Wildlife Laboratories, Inc. Pharmaceutical combination for and method of anesthetizing and immobilizing non-domesticated mammals
US8555875B2 (en) 2008-12-23 2013-10-15 Map Pharmaceuticals, Inc. Inhalation devices and related methods for administration of sedative hypnotic compounds
CN101921234B (zh) * 2009-06-12 2012-05-30 中国中化股份有限公司 一种制备美托咪啶的方法
CN102753532B (zh) 2009-12-09 2015-05-13 I-技术有限公司 美托咪定的制备方法
CN101805294B (zh) * 2010-01-12 2015-06-10 北京华禧联合科技发展有限公司 盐酸右美托咪定关键中间体的制备
RU2448095C1 (ru) * 2010-12-09 2012-04-20 Олег Геннадьевич Еремин Способ получения детомидина или его нетоксичных фармацевтически приемлемых солей
RU2448094C1 (ru) * 2010-12-09 2012-04-20 Олег Геннадьевич Еремин Улучшенный способ получения медетомидина или его нетоксичных фармацевтически приемлемых солей
KR101932206B1 (ko) 2011-07-22 2018-12-24 캠브렉스 칼스코가 아베 4-치환 이미다졸의 신규 제조방법
WO2013069025A1 (en) 2011-11-11 2013-05-16 Neon Laboratories Ltd. "process for the preparation of dexmedetomidine"
US8242158B1 (en) 2012-01-04 2012-08-14 Hospira, Inc. Dexmedetomidine premix formulation
WO2012172119A2 (en) * 2012-05-08 2012-12-20 Lonza Ltd Method for the preparation of medetomidine
CN104245679B (zh) * 2012-05-08 2016-03-02 隆萨有限公司 美托咪定的制备方法
DK2847157T3 (en) 2012-05-08 2016-02-08 Lonza Ag PROCEDURE FOR PREPARING 2- (2,3-DIMETHYLPHENYL) -1-PROPANAL
EA024425B1 (ru) * 2012-06-28 2016-09-30 Лонца Лтд. Способ получения 2-(2,3-диметилфенил)-1-пропаналя с использованием хлорацетона
AU2012285677B2 (en) 2012-06-28 2016-03-31 Lonza Ltd Method for preparation of medetomidine with chloroacetone
RU2646512C2 (ru) 2013-10-07 2018-03-05 ТЕЙКОКУ ФАРМА ЮЭсЭй, ИНК. Устройства для трансдермальной доставки дексмедетомидина и способы их применения
TWI629066B (zh) 2013-10-07 2018-07-11 帝國製藥美國股份有限公司 使用右美托咪啶經皮組成物用於治療注意力不足過動症、焦慮及失眠的方法及組成物
ES2847936T3 (es) 2013-10-07 2021-08-04 Teikoku Pharma Usa Inc Métodos y composiciones para el suministro transdérmico de una cantidad no sedante de dexmedetomidina
CN104447562A (zh) * 2014-03-27 2015-03-25 宁波天衡药业股份有限公司 一种制备盐酸右美托咪定关键中间体的新方法
CN107613977A (zh) 2015-05-06 2018-01-19 I-技术有限公司 用于控制鱼上寄生甲壳纲动物的美托咪定
US9717796B1 (en) 2016-04-20 2017-08-01 Slypharma, Llc Heat sterilizeable, premixed, ready to use dexmedetomidine solution packaged in a flexible plastic container
CN105884691B (zh) * 2016-06-02 2017-08-25 江苏恒瑞医药股份有限公司 一种制备右美托咪定及其中间体的方法
WO2018065288A1 (de) 2016-10-07 2018-04-12 Bayer Cropscience Aktiengesellschaft 2-[2-phenyl-1-(sulfonylmethyl)vinyl]-imidazo[4,5-b]pyridin-derivate und verwandte verbindungen als schädlingsbekämpfungsmittel im pflanzenschutz
WO2018130443A1 (de) 2017-01-10 2018-07-19 Bayer Aktiengesellschaft Heterocyclen-derivate als schädlingsbekämpfungsmittel
WO2018130437A1 (de) 2017-01-10 2018-07-19 Bayer Aktiengesellschaft Heterocyclen-derivate als schädlingsbekämpfungsmittel
US11603475B2 (en) 2017-03-29 2023-03-14 I-Tech Ab Antifouling article
CN108872431B (zh) * 2018-07-09 2021-03-23 成都倍特药业股份有限公司 一种检测4-(1-(2,5-二甲基苯基)乙基)-1h-咪唑或/和其盐酸盐的方法
US11160791B2 (en) 2018-11-01 2021-11-02 Medefil, Inc. Dexmedetomidine injection premix formulation in ready to use (RTU) bags
CN111217756B (zh) * 2019-12-11 2022-03-11 南京亿华药业有限公司 一种盐酸右美托咪定的制备方法
CN113896684A (zh) * 2020-07-06 2022-01-07 复旦大学 一种美托咪定的制备方法
WO2023182903A1 (ru) 2022-03-22 2023-09-28 Общество с ограниченной ответственностью "ВИК-здоровье животных" Способ получения медетомидина и его производных
CN114671811A (zh) * 2022-04-14 2022-06-28 南京正科医药股份有限公司 一种右美托咪定拆分副产物的外消旋化回收方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2946804A (en) * 1958-12-29 1960-07-26 Abbott Lab (5-methyl-4-imidazolyl)-diphenyl carbinol salts and lower alkyl quaternaries
BE793407A (fr) * 1971-12-28 1973-06-28 Hoechst Ag Imidazolyl - (2) -carbinols ayant une activite hypolipidemique et leur procede de preparation
AU518569B2 (en) * 1979-08-07 1981-10-08 Farmos-Yhtyma Oy 4-benzyl- and 4-benzoyl imidazole derivatives
GB2069481B (en) * 1980-02-13 1983-07-27 Farmos Oy Substituted imidazole derivatives
GB2092569B (en) * 1981-02-05 1984-09-19 Farmos Oy Substituted imidazole derivatives and their preparation and use
GB2101114B (en) * 1981-07-10 1985-05-22 Farmos Group Ltd Substituted imidazole derivatives and their preparation and use

Also Published As

Publication number Publication date
NZ201176A (en) 1985-08-16
GB2101114B (en) 1985-05-22
FI822140A0 (fi) 1982-06-15
DK630486A (da) 1986-12-29
US4544664A (en) 1985-10-01
HK8289A (en) 1989-02-03
DK160610B (da) 1991-04-02
KR860001864B1 (ko) 1986-10-24
FI77858B (fi) 1989-01-31
AU8562882A (en) 1983-01-13
EP0072615B1 (en) 1985-12-27
DK630486D0 (da) 1986-12-29
FI77858C (fi) 1989-05-10
JPS5818365A (ja) 1983-02-02
US4639464A (en) 1987-01-27
IE53244B1 (en) 1988-09-14
NO160439B (no) 1989-01-09
EP0072615A1 (en) 1983-02-23
DD207713A1 (de) 1984-03-14
GB2101114A (en) 1983-01-12
ATE17121T1 (de) 1986-01-15
BG60763B2 (bg) 1996-02-29
AU554125B2 (en) 1986-08-07
CA1184559A (en) 1985-03-26
NO160439C (no) 1989-04-19
KR840000507A (ko) 1984-02-22
IL66271A0 (en) 1982-11-30
DK158307B (da) 1990-04-30
SG65388G (en) 1989-06-16
DK158307C (da) 1990-10-08
NO822183L (no) 1983-01-11
IL66271A (en) 1987-02-27
SU1241990A3 (ru) 1986-06-30
FI822140L (fi) 1983-01-11
DK304382A (da) 1983-01-11
ZA824875B (en) 1983-05-25
DK160610C (da) 1991-09-02
DE3268111D1 (en) 1986-02-06
HU187773B (en) 1986-02-28
JPH0372621B2 (uk) 1991-11-19
US4826864A (en) 1989-05-02

Similar Documents

Publication Publication Date Title
UA5557A1 (uk) Спосіб отримання заміщенних похідних імідазолу
ES8304485A1 (es) Procedimiento de fabricacion de recipientes para el envasad o de comestibles y productos similares.
YU212784A (en) Process for producing substituted aminocyclo-butene-3,4-diones
ATA399781A (de) Vorrichtung zur verhinderung der verdrehung eines flexiblen schlauchgurtes in einem schlauchgurtfoerderer
AU557378B2 (en) Production of hydrogen by alga
IL63630A0 (en) Process for the manufacture of ammonia
IL67003A (en) Biochemical process for the production of cyclic dihydroxy compounds
ZA851552B (en) Benzisoselenazolethiones,processes for their preparation and pharmaceutical products containing these compounds
ZA821040B (en) Reactor for the production of gaseous products
GB2035380B (en) Process for the chemical deposition of gold by autocatalytic reduction
AU547481B2 (en) Process for generating synthesis gas
GB8405366D0 (en) Production of chemical compounds
IL73228A (en) Process for the production of 6-hydroxyethyl-2-substituted thio penem-3-carboxylates
HUT38623A (en) Process for production of derivatives of n-substituated neuramin-acid
AU8181782A (en) Electrolyzer for the production of hydrogen
ES8706693A1 (es) Procedimiento para la produccion de derivados del acido 7-amino-3-alcoximetil-3-cefem-4-carboxilico
EP0082006A3 (en) Method for producing vicinal dihalogenated products and uses thereof, and process for preparing epoxides using the same
GB2093722B (en) Catalyst for the production of 2-cyanopyrazine
AU1153283A (en) Chemical process
EP0040715A3 (en) Process for the production of acetaldehyde and methanol from the reaction mixture of methanol homologation
AU548371B2 (en) Polycyclic linked system containing hetero rings having oxygen atoms (derivatives of m.139,603)
JPS57174317A (en) Reaction accelerator for acid anhydride- hardening epoxide resins
HUT39183A (en) Herbicides containing as reagent derivatives of 4h-piridol (2,3-d) (1,3) oxazine-4-on and process for the production of the reagents
HUT38207A (en) Herbicides containing as reagent derivatives of cyclohexan-1,3-dion and process for production of the reagents
IL91420A0 (en) Process for the preparation of aryldimethyl(3-aryl-propyl)silanes