KR840004089A - 구아니디노 헤테로사이클릭페닐아미딘의 제조방법 - Google Patents

구아니디노 헤테로사이클릭페닐아미딘의 제조방법

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Publication number
KR840004089A
KR840004089A KR1019830001151A KR830001151A KR840004089A KR 840004089 A KR840004089 A KR 840004089A KR 1019830001151 A KR1019830001151 A KR 1019830001151A KR 830001151 A KR830001151 A KR 830001151A KR 840004089 A KR840004089 A KR 840004089A
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group
formula
compound
reaction
carried out
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KR1019830001151A
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English (en)
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비에티(외5) 주세페
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볼프강 호레트
인스티튜토 드 앙겔리 에스.피.에이
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Publication of KR840004089A publication Critical patent/KR840004089A/ko

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D275/00Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/02Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/061,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
    • C07D271/071,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole 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
    • C07D263/48Nitrogen atoms not forming part of a nitro radical
    • 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
    • C07D277/38Nitrogen atoms
    • C07D277/44Acylated amino or imino radicals
    • C07D277/48Acylated amino or imino radicals by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof, e.g. carbonylguanidines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D285/00Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01Five-membered rings
    • C07D285/02Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/081,2,4-Thiadiazoles; Hydrogenated 1,2,4-thiadiazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D285/00Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01Five-membered rings
    • C07D285/02Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/121,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
    • C07D285/1251,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • C07D285/135Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/535Organo-phosphoranes
    • C07F9/5355Phosphoranes containing the structure P=N-
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/54Quaternary phosphonium compounds
    • C07F9/5463Compounds of the type "quasi-phosphonium", e.g. (C)a-P-(Y)b wherein a+b=4, b>=1 and Y=heteroatom, generally N or O

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Cosmetics (AREA)

Abstract

내용 없음

Description

구아니디노 헤테로사이클릭페닐아미딘의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (9)

  1. 일반식(Ⅱ)의 화합물을 일반식(Ⅲ)의 화합물과 반응시킴을 특징으로 하여 일반식(Ⅰ)의 화합물 및 그의 토오토머 및 산부가염을 제조하는 방법.
    상기 일반식에서
    R, R1및 R2는 같거나 다르며, 각각 수소원자 또는 탄소수 1내지 4의 알킬그룹을 나타내며, R3는 산소, 유황, 또는 질소원자 등의 헤테로원자를 임의로 함유하는 직쇄 또는 측쇄 알킬그룹, 직쇄 또는 측쇄알킬닐 그룹, 알키닐그룹, 시아노그룹, 사이클로알킬 또는 지환족 알킬 그룹, 비사이클릭그룹, 아릴그룹, 헤테로사이클릭그룹을 나타내거나 R3및 R2는 이들이 부착된 질소원자와 함께 헤테로사이클릭그룹을 나타내며, R4는 수소원자, 탄소수 1 내지 4의 알킬 또는 알콕시 그룹 또는 할로겐원자를 나타내며, Het는 두개 또는 세개의 헤테로원자를 함유하는 치환되거나 비치환된 헤테로사이클릭 그룹을 나타내며 A는 메톡시 또는 에톡시 그룹을 나타낸다.
  2. 제1항에 있어서 불활성 유기용매 존재하에 반응을 수행하는 방법.
  3. 제2항에 있어서 불활성 유기용매가 에탄올, 디옥산 또는 아세톤인 방법.
  4. 제1 내지 3항의 어느 하나에 있어 반응을 20 내지 60℃에서 수행하는 방법.
  5. 일반식(Ⅵ)의 화합물을 상기 일반식(Ⅱ)의 아민과 반응시킴을 특징으로 하여 상기 일반식(Ⅰ)의 화합물을 제조하는 방법.
    상기 일반식에서 R2및 R3는 제1항에서 전술한 바와 같고 Y는 메틸 또는 에틸 그룹을 나타낸다.
  6. 제5항에 있어서 반응을 20 내지 80℃에서 수행하는 방법.
  7. 일반식(Ⅶa) 또는 (Ⅶb) 화합물을 일반식(Ⅳ)의 아민과 반응시킴을 특징으로 하여 상기 일반식(Ⅰ) 화합물을 제조하는 방법.
    상기 일반식에서 R, R1내지 R4및 Het는 제1항에서 전술한 바와 같고, B는 시아노, 아세틸, 카브에톡시 또는 카바밀 그룹을 나타낸다.
  8. 제7항에 있어서 물 또는 디메틸포름아미드 존재하에 반응을 수행하는 방법.
  9. 제7 및 8항에 있어서 반응을 실온에서 수행하는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019830001151A 1982-03-24 1983-03-22 구아니디노 헤테로사이클릭페닐아미딘의 제조방법 KR840004089A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT20356A/82 1982-03-24
IT20356/82A IT1200371B (it) 1982-03-24 1982-03-24 Guanidino eterociclifenilamidine,processi per la loro preparazione e loro impiego farmaceutico

Publications (1)

Publication Number Publication Date
KR840004089A true KR840004089A (ko) 1984-10-08

Family

ID=11165991

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019830001151A KR840004089A (ko) 1982-03-24 1983-03-22 구아니디노 헤테로사이클릭페닐아미딘의 제조방법

Country Status (24)

Country Link
US (2) US4548944A (ko)
EP (1) EP0089730B1 (ko)
JP (1) JPS58185574A (ko)
KR (1) KR840004089A (ko)
AT (1) ATE27455T1 (ko)
AU (1) AU562246B2 (ko)
CA (1) CA1190546A (ko)
DD (1) DD232704A5 (ko)
DE (2) DE89730T1 (ko)
DK (1) DK63183A (ko)
ES (3) ES8404982A1 (ko)
FI (1) FI78476C (ko)
GB (1) GB2116975B (ko)
GR (1) GR77435B (ko)
HU (1) HU187877B (ko)
IL (1) IL68204A (ko)
IT (1) IT1200371B (ko)
NO (1) NO159269C (ko)
NZ (1) NZ203663A (ko)
PL (2) PL138921B1 (ko)
PT (1) PT76432B (ko)
SU (2) SU1151208A3 (ko)
YU (2) YU43160B (ko)
ZA (1) ZA832016B (ko)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1210914B (it) * 1982-07-29 1989-09-29 Angeli Inst Spa Eterociclilfenilsolfonil e fosfonilamidine sostituite, procedimento per la loro preparazione e loro uso farmaceutico.
GB9125970D0 (en) * 1991-12-06 1992-02-05 Fujisawa Pharmaceutical Co New compounds
GB9211163D0 (en) * 1992-05-26 1992-07-08 Fujisawa Pharmaceutical Co New oxazole derivatives
US6787490B2 (en) * 2001-12-26 2004-09-07 Kimberly-Clark Worldwide, Inc. Glove donning delivery system
KR100969686B1 (ko) 2006-08-07 2010-07-14 한국과학기술연구원 신규한 티아졸계 화합물 및 이를 함유하는 t-형 칼슘 채널저해제
WO2022034121A1 (en) 2020-08-11 2022-02-17 Université De Strasbourg H2 blockers targeting liver macrophages for the prevention and treatment of liver disease and cancer

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54132566A (en) * 1978-01-18 1979-10-15 Ici Ltd Guanidine derivative*its manufacture and secretion controlling pharmaceutical composition containing it
EP0014057B1 (en) * 1979-01-18 1985-01-02 Imperial Chemical Industries Plc Guanidine derivatives, processes for their manufacture and pharmaceutical compositions containing them
IT1209431B (it) * 1980-11-28 1989-07-16 Angeli Inst Spa Imidazolilfenil amidine, processi per la loro preparazione e loro impiego farmaceutico, ed intermedi di preparazione.

Also Published As

Publication number Publication date
FI78476B (fi) 1989-04-28
NO831027L (no) 1983-09-26
FI78476C (fi) 1989-08-10
YU43418B (en) 1989-06-30
DE89730T1 (de) 1984-02-02
GB2116975B (en) 1985-08-14
ES520867A0 (es) 1984-05-16
NO159269B (no) 1988-09-05
ATE27455T1 (de) 1987-06-15
US4548944A (en) 1985-10-22
ES520868A0 (es) 1984-05-16
YU68983A (en) 1986-06-30
JPS58185574A (ja) 1983-10-29
YU152185A (en) 1986-06-30
FI830940L (fi) 1983-09-25
PL138921B1 (en) 1986-11-29
IL68204A (en) 1987-02-27
FI830940A0 (fi) 1983-03-22
GB2116975A (en) 1983-10-05
PT76432A (en) 1983-04-01
HU187877B (en) 1986-02-28
ES520869A0 (es) 1984-05-16
SU1151208A3 (ru) 1985-04-15
ES8404982A1 (es) 1984-05-16
DK63183A (da) 1983-09-25
ES8404980A1 (es) 1984-05-16
EP0089730B1 (en) 1987-05-27
CA1190546A (en) 1985-07-16
US4645841A (en) 1987-02-24
ZA832016B (en) 1984-11-28
SU1251804A3 (ru) 1986-08-15
PT76432B (en) 1986-02-06
IT1200371B (it) 1989-01-18
PL241145A1 (en) 1984-07-30
AU1273283A (en) 1983-09-29
EP0089730A3 (en) 1984-09-12
PL139031B1 (en) 1986-11-29
NO159269C (no) 1988-12-14
DD232704A5 (de) 1986-02-05
YU43160B (en) 1989-04-30
DE3371784D1 (en) 1987-07-02
EP0089730A2 (en) 1983-09-28
GB8307957D0 (en) 1983-04-27
ES8404981A1 (es) 1984-05-16
NZ203663A (en) 1986-01-24
PL246384A1 (en) 1984-11-19
DK63183D0 (da) 1983-02-14
GR77435B (ko) 1983-09-14
AU562246B2 (en) 1987-06-04
IT8220356A0 (it) 1982-03-24

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