KR840003632A - 푸릴옥사졸릴 아세트산 유도체의 제조방법 - Google Patents

푸릴옥사졸릴 아세트산 유도체의 제조방법 Download PDF

Info

Publication number
KR840003632A
KR840003632A KR1019830000770A KR830000770A KR840003632A KR 840003632 A KR840003632 A KR 840003632A KR 1019830000770 A KR1019830000770 A KR 1019830000770A KR 830000770 A KR830000770 A KR 830000770A KR 840003632 A KR840003632 A KR 840003632A
Authority
KR
South Korea
Prior art keywords
carbon atoms
alkyl
phenyl
compound
formula
Prior art date
Application number
KR1019830000770A
Other languages
English (en)
Other versions
KR900001423B1 (ko
Inventor
가즈오 마쓰모또 (외 1)
Original Assignee
마쓰바라 이찌로
다나베 세이야꾸 가부시끼 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
Application filed by 마쓰바라 이찌로, 다나베 세이야꾸 가부시끼 가이샤 filed Critical 마쓰바라 이찌로
Publication of KR840003632A publication Critical patent/KR840003632A/ko
Application granted granted Critical
Publication of KR900001423B1 publication Critical patent/KR900001423B1/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/52Radicals substituted by nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Diabetes (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Obesity (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

내용 없음

Description

푸릴옥사졸릴 아세트산 유도체의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (13)

  1. 일반식(II)의 화합물을 탈수적인 폐환 반응을 시킴을 특징으로하여 일반식(I-a)의 화합물을 제조하는 방법.
  2. 상기식에서, R1은 탄소수 1 내지 6의 알킬, 탄소수 5 내지 6의 시클로알킬, 페닐 또는 치환된 페닐(여기에서 치환된 페닐은 탄소수 1 내지 2의 알킬, 탄소수 1 내지 2의 알콕시 및 할로겐 중에서 선택한 1 또는 2개의 라디칼로 치환된 페닐그룹이다)이고, R3는 탄소수 1 내지 12의 알킬이다.
  3. 일반식(I-a)의 화합물을 가수분해시키고 필요시 생성물을 약제학적으로 허용될 수 있는 그의 염으로 전환시킴을 특징으로 하여 일반식(I-b)의 화합물 또는 약제학적을 허용될 수 있는 그의 염을 제조하는 방법.
  4. 상기식에서, R1은 탄소수 1 내지 6의 알킬, 탄소수 5 내지 6의 시클로알킬, 페닐 또는 치환된 페닐(여기에서 치환된 페닐은 탄소수 1 내지 2의 알킬, 탄소수 1 내지 2의 알콕시 및 할로겐 중에서 선택한 1 또는 2개의 라디칼로 치환된 페닐그룹이다)이고 R3는 탄소수 1 내지 12의 알킬이다.
  5. 일반식(I-b)의 화합물을 에스테르화시킴을 특징으로 하여 일반식(I-c)의 화합물을 제조하는 방법.
  6. 상기식에서, R1은 탄소수 1 내지 6의 알킬, 탄소수 5 내지 6의 시클로알킬, 페닐 또는 치환된 페닐(여기에서 치환된 페닐은 탄소수 1 내지 2의 알킬, 탄소수 1 내지 2의 알콕시 및 할로겐 중에서 선택한 1 또는 2개의 라디칼로 치환된 페닐그룹이다)이고 R4는 탄소수 1 내지 12의 알킬이다.
  7. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019830000770A 1982-02-26 1983-02-25 푸릴옥사졸릴아세트산 유도체의 제조방법 KR900001423B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP82-30921 1982-02-26
JP57030921A JPS58148882A (ja) 1982-02-26 1982-02-26 フリルオキサゾリル酢酸誘導体及びその製法

Publications (2)

Publication Number Publication Date
KR840003632A true KR840003632A (ko) 1984-09-15
KR900001423B1 KR900001423B1 (ko) 1990-03-09

Family

ID=12317149

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019830000770A KR900001423B1 (ko) 1982-02-26 1983-02-25 푸릴옥사졸릴아세트산 유도체의 제조방법

Country Status (14)

Country Link
US (1) US4642313A (ko)
EP (1) EP0087782B1 (ko)
JP (1) JPS58148882A (ko)
KR (1) KR900001423B1 (ko)
AT (1) ATE19879T1 (ko)
BG (1) BG39977A3 (ko)
CA (1) CA1194483A (ko)
DE (1) DE3363575D1 (ko)
DK (1) DK82583A (ko)
ES (1) ES520136A0 (ko)
HK (1) HK87188A (ko)
HU (1) HU193648B (ko)
SG (1) SG10688G (ko)
SU (1) SU1169536A3 (ko)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59152382A (ja) * 1983-02-18 1984-08-31 Tanabe Seiyaku Co Ltd フリルオキサゾリル酢酸誘導体
CA2160440C (en) * 1994-10-13 1998-08-25 Louis G. Lange, Iii Method of manufacturing non-absorbable synthetic sulfated polysaccharides
US7071174B1 (en) 1994-10-13 2006-07-04 Cv Therapeutics, Inc. Method and composition for inhibiting cholesterol esterase
CN101519386A (zh) * 2001-04-16 2009-09-02 田边三菱制药株式会社 高传导率钙-活化k通道开启剂

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE32084B1 (en) * 1967-06-07 1973-04-04 Wyeth John & Brother Ltd Thiazole derivatives
FI53314C (fi) * 1967-06-14 1978-04-10 Wyeth John & Brother Ltd Foerfarande foer framstaellning av farmaceutiskt anvaendbar 2-(fenyleller p-klorfenyl) oxazol-4-yl (aettiksyra -acetatsalt eller -acetamid)
GB1245087A (en) * 1967-10-26 1971-09-02 Wyeth John & Brother Ltd Heterocyclic compounds
US3578671A (en) * 1967-11-06 1971-05-11 Wyeth John & Brother Ltd Oxazoles
FR2068418A1 (en) * 1969-10-27 1971-08-27 Innothera Lab Sa 2-substd-5-amino isoxazole derivs
AR208400A1 (es) * 1974-03-13 1976-12-27 Yoshitomi Pharmaceutical Un metodo para producir nuevos acidos 5-alcoxi-4-oxazolalcanoicos 2-substituidos y sus esteres
JPS51110039A (ja) * 1975-02-28 1976-09-29 Yoshitomi Pharmaceutical Ketsuchushishitsutaishakaizenzai
GB1542315A (en) * 1976-08-13 1979-03-14 Wyeth John & Brother Ltd Process for preparing oxazoles
JPS5677268A (en) * 1979-11-28 1981-06-25 Yoshitomi Pharmaceut Ind Ltd Oxazoleacetic acid derivative
JPS57188587A (en) * 1981-05-15 1982-11-19 Tanabe Seiyaku Co Ltd Thienyloxazolylacetic acid derivative and its preparation

Also Published As

Publication number Publication date
BG39977A3 (en) 1986-09-15
DE3363575D1 (en) 1986-06-26
SU1169536A3 (ru) 1985-07-23
HU193648B (en) 1987-11-30
DK82583D0 (da) 1983-02-23
CA1194483A (en) 1985-10-01
SG10688G (en) 1988-07-01
JPS635027B2 (ko) 1988-02-01
HK87188A (en) 1988-11-04
EP0087782B1 (en) 1986-05-21
JPS58148882A (ja) 1983-09-05
ES8403891A1 (es) 1984-04-01
EP0087782A1 (en) 1983-09-07
ATE19879T1 (de) 1986-06-15
KR900001423B1 (ko) 1990-03-09
US4642313A (en) 1987-02-10
DK82583A (da) 1983-08-27
ES520136A0 (es) 1984-04-01

Similar Documents

Publication Publication Date Title
KR850000406A (ko) 4-클로로-2-페닐이미다졸-5-아세트산유도체의 제조방법
KR850003890A (ko) 1H-이미다조[4,5c]-퀴놀린-4-아민의 제조방법
ES2005746A6 (es) Un procedimiento para la preparacion de un haluro de piridinio.
KR850001905A (ko) 벤조시클로 알칸 유도체의 제조방법
KR920008018A (ko) 피페라진 유도체의 제조방법
KR830007562A (ko) 퀴놀린 카르복실산 유도체의 제조방법
KR840005101A (ko) 2-퀴놀린유도체의 제조방법
KR850004754A (ko) 3-인돌 카르복사미드 화합물류의 제조방법
KR840003632A (ko) 푸릴옥사졸릴 아세트산 유도체의 제조방법
GB1468913A (en) Sulphamoylbenzoic acid amides
KR850000421A (ko) 벤조티아제핀 유도체의 제조방법
KR830004320A (ko) 퀴나졸린 유도체의 제조방법
KR850002268A (ko) 3-인돌카르복스아미드 유도체의 제조방법
KR840004065A (ko) 2-시아노-2-프로페노산 및 그 유도체의 제조방법
KR840000530A (ko) 신규 벤조트리아졸의 제조방법
GB1505020A (en) Substituted 2-phenylimino-thiazolines a process for their preparation and their use as ectoparasiticides
KR840002821A (ko) N-(2,3-에폭시프로필렌)-n-아르알킬술폰아미드 유도체의 제조방법
KR840004432A (ko) 항 알레르기성 4H-퓨로[3,2-b] 인돌류의 제조방법
KR850006177A (ko) 신남산 유도체의 제조방법
KR850003407A (ko) 유기인산 에스테르 유도체의 제조방법
KR890002011A (ko) 5-할로 게노-6-아미노-니코틴산 할라이드. 이의 제조방법 및 용도
KR840005726A (ko) 고혈압 치료제로서 유용한 치환페닐 피페라진 화합물의 제조방법
KR840008024A (ko) 푸릴옥사졸일 아세트산 유도체의 제조방법
GB983607A (en) Novel 4,5-seco-steroid compounds and methods for the formation thereof
KR900006295A (ko) 할로게노-4-메틸피라졸류 및 그의 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
LAPS Lapse due to unpaid annual fee