KR830007670A - 페니실란오일옥시메틸 페니실라네이트 1, 1, 1', 1'-테트라옥사이드의 제조방법 - Google Patents

페니실란오일옥시메틸 페니실라네이트 1, 1, 1', 1'-테트라옥사이드의 제조방법 Download PDF

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Publication number
KR830007670A
KR830007670A KR1019810003366A KR810003366A KR830007670A KR 830007670 A KR830007670 A KR 830007670A KR 1019810003366 A KR1019810003366 A KR 1019810003366A KR 810003366 A KR810003366 A KR 810003366A KR 830007670 A KR830007670 A KR 830007670A
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South Korea
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penicillate
tetraoxide
general formula
compound represented
following general
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KR1019810003366A
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KR850001936B1 (ko
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크레베란드 비그함 에릭
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테렌스 제이. 갤락허
화이자 인코포레이티드
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D499/00Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

내용 없음

Description

페니실란오일옥시메틸 페니실라네이트 1, 1, 1', 1'-테트라옥사이드의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (5)

  1. 하기 일반식(VII)로 표시되는 화합물을 하기 일반식(III)으로 표시되는 화합물과 반응시킴을 특징으로 하는 페니실란 오일옥시메틸 페니실라네이트 1,1,1',1'-테트라옥사이드의 제조방법.
    (식중, M는 카르복실산업 생성 양이온이고, X는 탈리가 용이한 이탈기임).
  2. 제1항에 있어서 M이 나트륨, 칼륨, 칼슘, 바륨, 트리메틸아민, 트리에틸아민, 트리부틸아민, 디이소프로필에틸아민, N-메틸모르폴린, N-메틸피페미딘, N-메틸피롤리딘, N,N'-디메틸피페라진 또는 N-메틸-1,2,3,4-테트라히드로퀴놀린 염임을 특징으로 하는 방법.
  3. 제1항 또는 제2항에 있어서 X가 클로로, 브로모, 요오도, 탄소원자 1 내지 4의 알킬술포닐옥시, 페닐술포닐옥시 또는 톨릴술포닐옥시임을 특징으로 하는 방법.
  4. 제1항 내지 제3항에 있어서 반응을 0°내지 80℃온도하의 극성 유기 용매중에서 수행함을 특징으로 하는 방법.
  5. 제4항에 있어서 유기 극성 용매가 N,N-디메틸포름아미드, N,N-디메틸아세트아미드, N-메틸피롤리돈, 디메틸술폭시드 또는 핵사메틸포스포르아미드임을 특징으로 하는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019810003366A 1980-09-10 1981-09-09 페니실란오일옥시메틸 페니실라네이트 1, 1, 1', 1'-테트라옥사이드의 제조 방법 KR850001936B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US06/185,849 US4309347A (en) 1979-05-16 1980-09-10 Penicillanoyloxymethyl penicillanate 1,1,1',1'-tetraoxide
US185849 1980-09-10

Publications (2)

Publication Number Publication Date
KR830007670A true KR830007670A (ko) 1983-11-04
KR850001936B1 KR850001936B1 (ko) 1985-12-31

Family

ID=22682685

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019810003366A KR850001936B1 (ko) 1980-09-10 1981-09-09 페니실란오일옥시메틸 페니실라네이트 1, 1, 1', 1'-테트라옥사이드의 제조 방법

Country Status (18)

Country Link
US (1) US4309347A (ko)
EP (1) EP0047671B1 (ko)
JP (1) JPS5780387A (ko)
KR (1) KR850001936B1 (ko)
AR (1) AR226744A1 (ko)
AT (1) ATE8631T1 (ko)
AU (1) AU526672B2 (ko)
CA (1) CA1171849A (ko)
DE (1) DE3165077D1 (ko)
DK (1) DK159158C (ko)
ES (1) ES8206530A1 (ko)
FI (1) FI72120C (ko)
GR (1) GR75029B (ko)
IE (1) IE51550B1 (ko)
IL (1) IL63773A (ko)
PH (1) PH16982A (ko)
PT (1) PT73639B (ko)
YU (1) YU42698B (ko)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4376076A (en) * 1981-03-23 1983-03-08 Pfizer Inc. Bis-esters of 1,1-alkanediols with 6-beta-hydroxymethylpenicillanic acid 1,1-dioxide
US4444687A (en) * 1981-06-08 1984-04-24 Bristol-Myers Company 2β-Chloromethyl-2α-methylpenam-3α-carboxylic acid sulfone methylene diol mixed esters
US4540687A (en) * 1981-09-09 1985-09-10 Pfizer Inc. Antibacterial 6'-(2-amino-2-[4-acyloxyphenyl]acetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide compounds
US4582829A (en) * 1981-09-09 1986-04-15 Pfizer Inc. Antibacterial 6'-(2-amino-2-[4-acyloxyphenyl]acetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide compounds
US4457924A (en) * 1981-12-22 1984-07-03 Pfizer, Inc. 1,1-Alkanediol dicarboxylate linked antibacterial agents
US4452796A (en) * 1982-06-14 1984-06-05 Pfizer Inc. 6-Aminoalkylpenicillanic acid 1,1-dioxides as beta-lactamase inhibitors
US4536393A (en) * 1983-06-06 1985-08-20 Pfizer Inc. 6-(Aminomethyl)penicillanic acid 1,1-dioxide esters and intermediates therefor
US4502990A (en) * 1983-06-06 1985-03-05 Pfizer Inc. Process for 6-(aminomethyl)penicillanic acid 1,1-dioxide and derivatives thereof
US4521533A (en) * 1984-07-12 1985-06-04 Pfizer Inc. Salts of 6-alpha-(aminomethyl)penicillanic acid 1,1-dioxide esters and beta-lactam antibiotics
US4958212A (en) * 1988-12-30 1990-09-18 Texas Instruments Incorporated Trench memory cell
CN100384857C (zh) * 2003-11-28 2008-04-30 浙江永宁制药厂 耐β-内酰胺酶的头孢菌素酯化合物及其盐
JP4782489B2 (ja) * 2005-06-27 2011-09-28 トヨタ紡織株式会社 フィルタ用濾材

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE34948B1 (en) * 1970-03-12 1975-10-01 Leo Pharm Prod Ltd New penicillin esters
GB1303491A (ko) 1970-03-24 1973-01-17
GB1335718A (en) * 1971-05-05 1973-10-31 Leo Pharm Prod Ltd Penicillin esters salts thereof and methods for their preparation
GB1578128A (en) 1976-03-30 1980-11-05 Leo Pharm Prod Ltd Amidinopenicillanoyloxyalkyl amoxycillinates
IN149747B (ko) 1977-06-07 1982-04-03 Pfizer
IE49880B1 (en) * 1979-02-13 1986-01-08 Leo Pharm Prod Ltd Penicillin derivatives
BE881675A (fr) 1979-02-13 1980-08-12 Leo Pharm Prod Ltd B-lactames derives de l'acide penicillanique leur preparation et leurs utilisations therapeutiques
US4244951A (en) * 1979-05-16 1981-01-13 Pfizer Inc. Bis-esters of methanediol with penicillins and penicillanic acid 1,1-dioxide

Also Published As

Publication number Publication date
IE812076L (en) 1982-03-10
DK400381A (da) 1982-03-11
GR75029B (ko) 1984-07-12
AU526672B2 (en) 1983-01-27
IL63773A (en) 1985-02-28
DK159158C (da) 1991-03-11
KR850001936B1 (ko) 1985-12-31
ES505345A0 (es) 1982-08-16
PT73639A (en) 1981-10-01
YU214581A (en) 1983-06-30
AR226744A1 (es) 1982-08-13
JPS643196B2 (ko) 1989-01-19
US4309347A (en) 1982-01-05
PH16982A (en) 1984-05-04
EP0047671B1 (en) 1984-07-25
DE3165077D1 (de) 1984-08-30
FI72120C (fi) 1987-04-13
IL63773A0 (en) 1981-12-31
DK159158B (da) 1990-09-10
CA1171849A (en) 1984-07-31
EP0047671A1 (en) 1982-03-17
PT73639B (en) 1983-04-29
AU7508281A (en) 1982-03-18
YU42698B (en) 1988-10-31
JPS5780387A (en) 1982-05-19
ATE8631T1 (de) 1984-08-15
ES8206530A1 (es) 1982-08-16
FI812803L (fi) 1982-03-11
IE51550B1 (en) 1987-01-07
FI72120B (fi) 1986-12-31

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