KR870011144A - 세팔로스포린 유도체의 제조방법 - Google Patents

세팔로스포린 유도체의 제조방법 Download PDF

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Publication number
KR870011144A
KR870011144A KR1019860003550A KR860003550A KR870011144A KR 870011144 A KR870011144 A KR 870011144A KR 1019860003550 A KR1019860003550 A KR 1019860003550A KR 860003550 A KR860003550 A KR 860003550A KR 870011144 A KR870011144 A KR 870011144A
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KR
South Korea
Prior art keywords
formula
cephalosporin derivative
preparing cephalosporin
compound
organic base
Prior art date
Application number
KR1019860003550A
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English (en)
Other versions
KR890000523B1 (ko
Inventor
장문호
김봉진
김성각
김완주
Original Assignee
한국 과학 기술원
이정오
한국과학기술원
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 한국 과학 기술원, 이정오, 한국과학기술원 filed Critical 한국 과학 기술원
Priority to KR1019860003550A priority Critical patent/KR890000523B1/ko
Priority to US07/001,875 priority patent/US4835267A/en
Publication of KR870011144A publication Critical patent/KR870011144A/ko
Application granted granted Critical
Publication of KR890000523B1 publication Critical patent/KR890000523B1/ko

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/36Methylene radicals, substituted by sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/26Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/26Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
    • C07D501/32Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by an araliphatic carboxylic acid, which is substituted on the aliphatic radical by hetero atoms

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Cephalosporin Compounds (AREA)

Abstract

내용 없음

Description

세팔로스포린 유도체의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (2)

  1. 다음의 일반식(Ⅳ)의 실릴화물에 일반식(Ⅲ)화합물과 일반식(Ⅱ)의 화합물을 유기 염기 존재하에 반응시킴을 특징으로 하는 일반식(Ⅰ)의 세팔로스포린 유도체의 제조방법.
    상기 각 식에서,
    R1은 수소 또는를 의미하며, R2는 메틸, 에틸, 프로필, 페닐을 나타내고,
  2. 제 1 항에 있어서 유기 염기를 트리에틸아민 또는 피리딘 또는 이소프로필아민 또는 디메틸아민 또는 디메틸아미노 피리딘 중에서 선택하여 사용하는 것을 특징으로 하는 방법.
    ※ 참고사항 : 최초출원내용에 의하여 공개하는 것임.
KR1019860003550A 1986-05-07 1986-05-07 세팔로스포린 유도체의 제조방법 KR890000523B1 (ko)

Priority Applications (2)

Application Number Priority Date Filing Date Title
KR1019860003550A KR890000523B1 (ko) 1986-05-07 1986-05-07 세팔로스포린 유도체의 제조방법
US07/001,875 US4835267A (en) 1986-05-07 1987-01-09 Process for the preparation of cephalosporin derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019860003550A KR890000523B1 (ko) 1986-05-07 1986-05-07 세팔로스포린 유도체의 제조방법

Publications (2)

Publication Number Publication Date
KR870011144A true KR870011144A (ko) 1987-12-21
KR890000523B1 KR890000523B1 (ko) 1989-03-20

Family

ID=19249827

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019860003550A KR890000523B1 (ko) 1986-05-07 1986-05-07 세팔로스포린 유도체의 제조방법

Country Status (2)

Country Link
US (1) US4835267A (ko)
KR (1) KR890000523B1 (ko)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES411867A1 (es) * 1973-02-21 1976-01-01 Gema Sa Procedimiento para la preparacion de agentes sililantes.

Also Published As

Publication number Publication date
US4835267A (en) 1989-05-30
KR890000523B1 (ko) 1989-03-20

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