KR840006674A - 디디히드로 밀베마이신 유도체의 제조방법 - Google Patents

디디히드로 밀베마이신 유도체의 제조방법 Download PDF

Info

Publication number
KR840006674A
KR840006674A KR1019830005571A KR830005571A KR840006674A KR 840006674 A KR840006674 A KR 840006674A KR 1019830005571 A KR1019830005571 A KR 1019830005571A KR 830005571 A KR830005571 A KR 830005571A KR 840006674 A KR840006674 A KR 840006674A
Authority
KR
South Korea
Prior art keywords
group
formula
alkyl
compound
alkyl group
Prior art date
Application number
KR1019830005571A
Other languages
English (en)
Other versions
KR880001868B1 (ko
Inventor
데준 야 이 (외 3)
Original Assignee
가와무라 요시부미
상꾜 가부시기 가이샤
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=16523775&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=KR840006674(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by 가와무라 요시부미, 상꾜 가부시기 가이샤 filed Critical 가와무라 요시부미
Publication of KR840006674A publication Critical patent/KR840006674A/ko
Application granted granted Critical
Publication of KR880001868B1 publication Critical patent/KR880001868B1/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/20Carbocyclic rings
    • C07H15/22Cyclohexane rings, substituted by nitrogen atoms
    • C07H15/238Cyclohexane rings substituted by two guanidine radicals, e.g. streptomycins
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/01Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing oxygen
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H13/00Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Plant Pathology (AREA)
  • Wood Science & Technology (AREA)
  • Environmental Sciences (AREA)
  • Zoology (AREA)
  • Veterinary Medicine (AREA)
  • Dentistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Saccharide Compounds (AREA)

Abstract

내용 없음

Description

디디히드로 밀베마이신 유도체의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (10)

  1. 하기 일반식(Ⅲ)의 화합물을 하기 일반식(Ⅳ)의 옥심화제 또는 그의 염과 반응시키고, 생성된 일반식(Ⅱ)의 화합물(R2가 수소원자임)을 산할라이드 또는 이소시아네이트와 임의로 반응시켜 화합물(Ⅱ)의 에스테르를 제조함을 특징으로 하는 하기 일반식(Ⅱ)의 화합물 및 그의 염 및 에스테르의 제조방법.
  2. 상기 식중, R1은 메틸기, 에틸기 또는 이소프로필기 이고, R2는 수소원자, C1-C6알킬기, 하나 이상의 C1-C6알킬, 할로겐 또는 니트로 치환제를 임의로 갖는 아르알킬기, 또는 일반식 -CH2COOR3의 기(R3는 수소원자 또는 C1-C6알킬기를 나타낸다)이며, R2는 수소원자를 나타낸다.
  3. 제1항에 있어서, 일반식(Ⅲ)의 화합물을 일반식(Ⅳ)의 옥심화제 또는 그의 염과 반응시킴을 특징으로 하는 일반식(Ⅱ)의 화합물(R2는 수소, C1-C6알킬기, 벤질 또는 카르복시 메틸기를 나타낸다)의 제조방법.
  4. 제1항에 있어서, 일반식(Ⅲ)의 화합물을 히드록시아민 또는 그의 염과 반응시키고, 생성된 일반식(Ⅱ)의 화합물(R2는 수소위자를 나타냄)을 일반식 R2a-X(R2a는 하기와 같고, X는 할로겐 원자이다)의 산할라이드와 반응시킴을 특징으로 하는 하기 일반식(Ⅱa)의 화합물의 제조방법.
  5. 상기식중, R1은 메틸, 에틸 또는 이소프로필기를 나타내고, R2a는, 일반식 -COR4의 기(식중 R4는 C1-C6알킬기, 하나 이상의 C1-C6알킬, 할로겐 또는 니트로 치환체를 임의로 갖는 아르알킬기, 하나이상의 C1-C6알킬, 할로겐, 니트로, 카르복시 또는 C2-C7알콕시 카르보닐 치환제를 임의로 갖는 폐닐기, 또는 일반식 -(CH2)nCOOR5의 기(n은 1∼3의 정수이고, R5는 수소원자 또는 C1-C6알킬기이다)를 나타낸다); 일반식 -CONR6'R7'의 기(식중 R6'는 C1-C6알킬기를 나타내고,'R7'는 C1-C6알킬기, 아릴기 또는 일반식 -CH(R8)COOR9의 기(식중 R8및 R9는 같거나 서로 다르고, 각각 수소 또는 C1-C6알킬기이다)를 나타낸다); 일반식 -COOR10의 기(식중 R10은 C1-C6알킬기, 하나 이상의 C1-C6알킬, 할로겐 또는 니트로 치환제를 임의로 갖는 아르알킬기, 아릴기 또는 임의 보호된 슈가 알콜로부터 오메가 히드록시기를 제거함으로써 유도된 기를 나타낸다); 일반식 -SO2R11의 기 (식중 R10은 C1-C6알킬기 또는 아릴기를 나타낸다); 또는 일반식 -(Y1=)P(-Y2-R13)2의 기(식중 Y1및 Y2는 같거나 서로 다르고, 각각 산소 또는 황을 나타내며, Y2로 표시된 두 원자는 같거나 서로 다르고, R12로 표시된 각기는 같거나 서로 다르며 C1-C6알킬기를 나타낸다)를 나타낸다.
  6. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019830005571A 1982-11-25 1983-11-24 디데히드로 밀베마이신 유도체의 제조방법 KR880001868B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP206462/1982 1982-11-25
JP206462 1982-11-25
JP57206462A JPS59108785A (ja) 1982-11-25 1982-11-25 ミルベマイシン類の5−オキシム誘導体

Publications (2)

Publication Number Publication Date
KR840006674A true KR840006674A (ko) 1984-12-01
KR880001868B1 KR880001868B1 (ko) 1988-09-23

Family

ID=16523775

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019830005571A KR880001868B1 (ko) 1982-11-25 1983-11-24 디데히드로 밀베마이신 유도체의 제조방법

Country Status (12)

Country Link
US (1) US4547520A (ko)
EP (1) EP0110667B1 (ko)
JP (1) JPS59108785A (ko)
KR (1) KR880001868B1 (ko)
AR (1) AR240048A1 (ko)
BR (1) BR8306467A (ko)
CA (1) CA1215360A (ko)
DE (1) DE3369517D1 (ko)
IE (1) IE56309B1 (ko)
IL (1) IL70301A (ko)
NZ (1) NZ206399A (ko)
ZA (1) ZA838761B (ko)

Families Citing this family (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4579864A (en) * 1984-06-11 1986-04-01 Merck & Co., Inc. Avermectin and milbemycin 13-keto, 13-imino and 13-amino derivatives
GB2168345B (en) * 1984-12-14 1988-05-25 Ciba Geigy Ag Pesticidal 13b-substituted milbemycin derivatives
ES8802229A1 (es) * 1985-04-30 1988-04-16 Glaxo Group Ltd Un procedimiento para preparar nuevos derivados lactonicos macrociclicos.
US4789684A (en) * 1985-05-02 1988-12-06 Merck & Co., Inc. Anthelmintic fermentation products of microorganisms
JPS6289685A (ja) 1985-05-31 1987-04-24 Sankyo Co Ltd 13−ハロゲンミルベマイシン誘導体
US5185456A (en) * 1986-03-12 1993-02-09 American Cyanamid Company Macrolide compounds
GB8606108D0 (en) * 1986-03-12 1986-04-16 Glaxo Group Ltd Chemical compounds
US5336789A (en) * 1986-03-12 1994-08-09 American Cyanamid Company Macrolide compounds
NZ219576A (en) * 1986-03-12 1989-01-06 Glaxo Group Ltd Milbemycin derivatives and pharmaceutical, veterinary, and pesticidal compositions
RU2024527C1 (ru) * 1986-03-25 1994-12-15 Санкио Компани Лимитед Способ получения макролидных соединений
CA1296329C (en) * 1986-06-06 1992-02-25 Derek R. Sutherland Macrolide compounds
US4916154A (en) * 1986-09-12 1990-04-10 American Cyanamid Company 23-Imino derivatives of LL-F28249 compounds
US4877888A (en) * 1986-09-12 1989-10-31 American Cyanamid Company 13-deoxy-23-imino derivatives of 13-deoxy C-076-aglycone compounds
US4849446A (en) * 1986-09-12 1989-07-18 American Cyanamid Company 23-imino derivatives of 23-keto compounds
US4886784A (en) * 1986-09-12 1989-12-12 American Cyanamid Company Novel 23-imino derivatives of 23-keto compounds
US5183749A (en) * 1987-02-04 1993-02-02 Sankyo Company, Ltd. Microbial process for the preparation of milbemycin derivatives
ES2053797T3 (es) * 1987-02-04 1994-08-01 Ciba Geigy Ag Procedimiento microbiano para la obtencion de derivados de milbemicina.
US4897416A (en) * 1987-02-18 1990-01-30 Ciba-Geigy Corporation Insecticides and parasiticides
US4886829A (en) * 1987-03-06 1989-12-12 American Cyanamid Company 23-Oxo (keto) and 23-imino derivatives of mono- and diepoxy LL-F28249 compounds
US4831017A (en) * 1987-06-29 1989-05-16 Merck & Co., Inc. Increased litter size in monogastric domestic animals after treatment in mid-gestation of gravid female with avermectin or milbemycin compound
US5192777A (en) * 1987-09-11 1993-03-09 American Cyanamid Company Macrolide compounds
US4847243A (en) * 1987-10-08 1989-07-11 Merck & Co., Inc. Treatment for fescue toxicosis in grazing animals
NZ229052A (en) * 1988-05-10 1991-03-26 American Cyanamid Co Milbemycin derivatives, use for combating pests
US5428034A (en) * 1988-09-02 1995-06-27 Sankyo Co., Ltd. Milbemycin derivatives, their preparation and their use
US5015630A (en) * 1989-01-19 1991-05-14 Merck & Co., Inc. 5-oxime avermectin derivatives
NZ232422A (en) * 1989-02-16 1992-11-25 Merck & Co Inc 13-ketal milbemycin derivatives and parasiticides
JP2622197B2 (ja) * 1990-03-01 1997-06-18 三共株式会社 13−エーテル置換ミルベマイシン誘導体
JPH085894B2 (ja) * 1990-03-01 1996-01-24 三共株式会社 ミルベマイシンエーテル誘導体
RU2086552C1 (ru) * 1991-12-18 1997-08-10 Санкио Компани Лимитед Производные 13-(замещенного тио)ацетоксимилбемицина, способ их получения, инсектицидная композиция и способ защиты растений
AU660205B2 (en) 1991-12-23 1995-06-15 Virbac, Inc Systemic control of parasites
US5439924A (en) * 1991-12-23 1995-08-08 Virbac, Inc. Systemic control of parasites
US5362862A (en) * 1993-09-29 1994-11-08 Merck & Co., Inc. Process for 4"-EPI-acetylamino-4"-deoxy-5-oximinoavermectin-B1
US5614470A (en) * 1994-04-01 1997-03-25 Sankyo Company, Limited 13-substituted milbemycin derivatives, their preparation and their use
CA2213612C (en) * 1995-02-24 2008-07-15 Novartis Ag Composition for controlling parasites
AU707152B2 (en) * 1995-09-29 1999-07-01 Novartis Animal Health K.K. 13-substituted milbemycin 5-oxime derivatives, their preparation and their use against insects and other pests
US6124359A (en) * 1995-10-20 2000-09-26 Mycogen Corporation Materials and methods for killing nematodes and nematode eggs
US5674897A (en) * 1995-10-20 1997-10-07 Mycogen Corporation Materials and methods for controlling nematodes
WO1999017760A2 (en) 1997-10-02 1999-04-15 Microcide Pharmaceuticals, Inc. Fungal or mammalian cell efflux pump inhibitors for enhancing susceptibility of the cell to a drug
US6875727B2 (en) 1997-12-23 2005-04-05 Syngenta Crop Protection, Inc. Use of macrolides in pest control
AU777932B2 (en) * 1997-12-23 2004-11-04 Syngenta Participations Ag Use of macrolides in pest control
NZ505208A (en) * 1997-12-23 2003-07-25 Novartis Ag Use of macrolides in pest control
WO2001083500A1 (en) 2000-04-27 2001-11-08 Sankyo Company, Limited 13-substituted milbemycin derivatives, their preparation and their use against insects and other pests
US6887900B2 (en) 2002-03-04 2005-05-03 Divergence, Inc. Nematicidal compositions and methods
US20040157803A1 (en) * 2002-03-04 2004-08-12 Williams Deryck J. Nematicidal fatty acid and fatty acid ester related compounds
TWI366442B (en) * 2003-07-30 2012-06-21 Novartis Ag Palatable ductile chewable veterinary composition
US7368629B2 (en) * 2004-02-04 2008-05-06 Divergence, Inc. Nucleic acids encoding anthelmintic agents and plants made therefrom
US20070149464A1 (en) * 2005-06-15 2007-06-28 Pfizer Inc. Combination
EP1849363A1 (en) * 2006-03-09 2007-10-31 Cheminova A/S Synergistic combination of glutamate- and GABA-gated chloride agonist pesticide and at least one of Vitamin E or Niacin
EP2886640A1 (en) 2013-12-18 2015-06-24 Riga Technical University Process for isolation of milbemycins A3 and A4
CN104327094B (zh) * 2014-10-30 2016-08-17 湖北宏中药业有限公司 一种米尔贝肟的分离纯化方法
CN111094296A (zh) * 2017-07-24 2020-05-01 浙江海正药业股份有限公司 一种米尔贝a4肟晶型a及其制备方法
KR20190014439A (ko) 2017-08-02 2019-02-12 김도경 밑실을 구비하지 않은 봉제구조, 및 그를 위한 봉제장치

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3950360A (en) * 1972-06-08 1976-04-13 Sankyo Company Limited Antibiotic substances
US4093629A (en) * 1977-04-11 1978-06-06 Merck & Co., Inc. Derivatives of antibiotic substance milbemycin and processes therefor
NZ186851A (en) * 1977-04-11 1984-12-14 Merck & Co Inc Glycosyloxy derivatives of milbemycin and parasiticidal compositions
US4171314A (en) * 1977-12-19 1979-10-16 Merck & Co., Inc. 13-Halo and 13-deoxy C-076 compounds
JPS57120589A (en) * 1981-01-20 1982-07-27 Sankyo Co Ltd 5-methoxy and 5-lower alkanoyloxy derivative, its preparation and acaricide and parasiticide
JPS57139081A (en) * 1981-02-23 1982-08-27 Sankyo Co Ltd 5-alkylcarbamoyloxy and 5-alkanesulfonyloxy derivative of antibiotic substance b-41 and preparation thereof
JPS57139080A (en) * 1981-02-23 1982-08-27 Sankyo Co Ltd 14,15-epoxy derivative of antibiotic substance b-41 and its preparation
JPS57139079A (en) * 1981-02-23 1982-08-27 Sankyo Co Ltd 8,9-epoxy derivative of antibiotic substance b-41 and its preparation
US4423209A (en) * 1982-02-26 1983-12-27 Merck & Co., Inc. Processes for the interconversion of avermectin compounds

Also Published As

Publication number Publication date
JPS59108785A (ja) 1984-06-23
KR880001868B1 (ko) 1988-09-23
IE832762L (en) 1984-05-25
EP0110667B1 (en) 1987-01-28
ZA838761B (en) 1984-08-29
IL70301A0 (en) 1984-02-29
US4547520A (en) 1985-10-15
NZ206399A (en) 1986-02-21
AR240048A1 (es) 1990-01-31
DE3369517D1 (en) 1987-03-05
BR8306467A (pt) 1984-06-26
EP0110667A1 (en) 1984-06-13
IE56309B1 (en) 1991-06-19
CA1215360A (en) 1986-12-16
IL70301A (en) 1987-09-16

Similar Documents

Publication Publication Date Title
KR840006674A (ko) 디디히드로 밀베마이신 유도체의 제조방법
ATE910T1 (de) Derivate des 3.5-dihydroxypentansaeureesters mit antihyperlipaemischer aktivitaet, ihre herstellung und sie enthaltende pharmazeutische zusammensetzungen.
KR910002800A (ko) 4-아실록시퀴놀린 유도체와 이를 함유하는 살충 또는 살비조성물
KR860000243A (ko) 아민유도체의 제조방법
KR830002699A (ko) 신규의 안트라센-9,10-비스-카르보닐-히드라존 및 그 유도체 제조방법
KR840006482A (ko) 디히드로피라졸로 [3,4-b]피리딘 유도체의 제조방법
KR840000521A (ko) 3-메틸플라본-8-카르복실산 에스테르류의 제조방법
KR840004104A (ko) 페닐 피페라진 유도체의 제조방법
GB1491825A (en) Hindered hydroxyphenylalkanoates of substituted isopropanols and stabilized compositions
KR840005453A (ko) 펜엠 유도체의 제조방법
KR850006176A (ko) (아릴티오) 피리딜 알칼올 유도체의 제조방법
IE44184L (en) Imidazole derivatives
KR830006160A (ko) 1-아릴-사이클로프로판-1-카복실산 에스테르의 제조방법
KR840005107A (ko) 피리미디온 및 그의 산부가염의 제조방법
KR870004038A (ko) 제초제 화합물의 제조방법
KR930007880A (ko) 비스(페닐)에탄 유도체
KR830001900A (ko) 페닐모르판과 그의 중간물질및 제조방법
KR840008647A (ko) 대칭 1,4-디하이드로피리딘디카복실 에스테르의 제조방법
KR920700210A (ko) 신규 이미다졸 유도체, 그의 제법 및 그의 의약용도
KR840002821A (ko) N-(2,3-에폭시프로필렌)-n-아르알킬술폰아미드 유도체의 제조방법
KR840001154A (ko) 1,2-디티올-3-일리덴 암모늄 유도체의 제조방법
KR950032107A (ko) 헤테로치환된 아세탈의 제조방법
JPS57183776A (en) Preparation of mycophenolic acid derivative
KR830006293A (ko) 신규 폴리아자 헤테로고리 화합물의 제조방법
KR870007107A (ko) 구리 카르복실레이트를 산화제로 사용하는 아민의 산화 카보닐화에 의한 우레탄의 제조방법.

Legal Events

Date Code Title Description
A201 Request for examination
G160 Decision to publish patent application
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20030923

Year of fee payment: 16

EXPY Expiration of term