KR930007954A - Alkenyl cephalosporins and preparation methods thereof - Google Patents

Alkenyl cephalosporins and preparation methods thereof Download PDF

Info

Publication number
KR930007954A
KR930007954A KR1019910018791A KR910018791A KR930007954A KR 930007954 A KR930007954 A KR 930007954A KR 1019910018791 A KR1019910018791 A KR 1019910018791A KR 910018791 A KR910018791 A KR 910018791A KR 930007954 A KR930007954 A KR 930007954A
Authority
KR
South Korea
Prior art keywords
group
hydrogen
general formula
compound
alkenyl
Prior art date
Application number
KR1019910018791A
Other languages
Korean (ko)
Other versions
KR930007812B1 (en
Inventor
장문호
강한영
고훈영
배애님
조용서
Original Assignee
박원희
한국과학기술연구원
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 박원희, 한국과학기술연구원 filed Critical 박원희
Priority to KR1019910018791A priority Critical patent/KR930007812B1/en
Publication of KR930007954A publication Critical patent/KR930007954A/en
Application granted granted Critical
Publication of KR930007812B1 publication Critical patent/KR930007812B1/en

Links

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
    • C07D501/02Preparation
    • C07D501/04Preparation from compounds already containing the ring or condensed ring systems, e.g. by dehydrogenation of the ring, by introduction, elimination or modification of substituents

Landscapes

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

Abstract

본 발명은 다음 일반식(Ⅰ)로 표시되는 신규한알 케닐세팔로스포린 및 그 제조방법에 관한 것이다.The present invention relates to a novel al kenyl cephalosporin represented by the following general formula (I) and a method for producing the same.

식 중 R1은 수소, 트리틸, 3급 부톡시카르보닐, 포르밀이고, R2는 수소, 탄소수 1~4의 알킬, 알콕시카보닐메틸, 카르복시메틸, 1-카르복시에틸, 1-카르복시-1-메틸에틸, 탄소수 3~9의 시클로알킬기이고, R3는 수소, 알킬기, Na, K이고, R4및 R5는 수소 또는 대페닐메틸, 파라메톡시벤질임.Wherein R 1 is hydrogen, trityl, tert-butoxycarbonyl, formyl, R 2 is hydrogen, alkyl of 1 to 4 carbon atoms, alkoxycarbonylmethyl, carboxymethyl, 1-carboxyethyl, 1-carboxy- 1-methylethyl, a cycloalkyl group having 3 to 9 carbon atoms, R 3 is hydrogen, an alkyl group, Na, K, R 4 and R 5 are hydrogen or large phenylmethyl, paramethoxybenzyl.

본 발명의 일반식(Ⅰ)로 표시되는 알케닐세팔로 스포린은 다음과 같은 반응공정에 따라 제조한다.Alkenyl cephalosporin represented by the general formula (I) of the present invention is prepared according to the following reaction process.

Description

알케닐 세팔로스포린 및 그 제조방법Alkenyl cephalosporins and preparation methods thereof

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (3)

다음 일반식(Ⅰ)로 표시되는 알케닐세팔로스포린 및 약제학적으로 허용되는 그 염.Alkenyl cephalosporins represented by the following general formula (I) and pharmaceutically acceptable salts thereof. 상기 일반식(Ⅰ)에 있어서 R1은 수소, 트리틸기, 3급 부톡시카르보닐기 또는 포르밀기이고, R2는 수소, 탄소수 1~4의 알킬기, 알콕시카보닐메틸기, 카르복시메틸기, 1-카르복시에틸기, 1-카르복시-1-메틸에틸기, 탄소수 3~9의 시클로알킬기이고, R3는 수소, Na, K, 파라-메톡시벤질기, 디페닐메틸기이고, R4와 R5는 수소, 아세틸기, 파라-메톡시벤질기, 벤질기, 메틸렌기 또는 아실기임.In said general formula (I), R <1> is hydrogen, a trityl group, tertiary butoxycarbonyl group, or formyl group, R <2> is hydrogen, a C1-C4 alkyl group, an alkoxycarbonylmethyl group, a carboxymethyl group, 1-carboxyethyl group , A 1-carboxy-1-methylethyl group, a cycloalkyl group having 3 to 9 carbon atoms, R 3 is hydrogen, Na, K, para-methoxybenzyl group, diphenylmethyl group, R 4 and R 5 are hydrogen, an acetyl group , Para-methoxybenzyl group, benzyl group, methylene group or acyl group. 일반식(Ⅲ)의 알데히드 화합물과 일반식(Ⅱ)의 포스포늄염을 반응시켜 일반식(Ⅳ)의 3-세펨화합물을 얻은후, 이 화합물(Ⅳ)을 탈아실화 반응을 시키는 일반식(Ⅴ)의 7-아미노-3-세펨유도체의 제조방법.After reacting the aldehyde compound of general formula (III) with the phosphonium salt of general formula (II) to obtain 3-cefem compound of general formula (IV), the compound (IV) is subjected to deacylation reaction (V). 7-amino-3-cepem derivative of the). 상기식에서, R3, R4및 R5는 각각 제1항에서 정의한 것과 동일함.Wherein R 3 , R 4 and R 5 are the same as defined in claim 1, respectively. 일반식(Ⅵ)의 화합물과 일반식(Ⅴ)의 화합물을 아실화 반응을 시키는 일반식(Ⅰ)의 알케닐세팔로 스포린의 제조방법.A process for producing alkenyl cephalosporin of formula (I) wherein the compound of formula (VI) and a compound of formula (V) are subjected to acylation reaction. 상기식에서, R2, R3, R4및 R5는 각각 제1항에서 정의한 것과 동일함.Wherein R 2 , R 3 , R 4 and R 5 are the same as defined in claim 1, respectively. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019910018791A 1991-10-25 1991-10-25 Process for preparing alkenyl cephalosporin KR930007812B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019910018791A KR930007812B1 (en) 1991-10-25 1991-10-25 Process for preparing alkenyl cephalosporin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019910018791A KR930007812B1 (en) 1991-10-25 1991-10-25 Process for preparing alkenyl cephalosporin

Publications (2)

Publication Number Publication Date
KR930007954A true KR930007954A (en) 1993-05-20
KR930007812B1 KR930007812B1 (en) 1993-08-20

Family

ID=19321732

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019910018791A KR930007812B1 (en) 1991-10-25 1991-10-25 Process for preparing alkenyl cephalosporin

Country Status (1)

Country Link
KR (1) KR930007812B1 (en)

Also Published As

Publication number Publication date
KR930007812B1 (en) 1993-08-20

Similar Documents

Publication Publication Date Title
KR910001037A (en) Phospholipase A2 Inhibitors
KR850001725A (en) Method for preparing carboxylic ester
KR850001905A (en) Method for preparing benzocyclo alkan derivatives
KR890016061A (en) Peptide derivatives
KR850004754A (en) Method for producing 3-indole carboxamide compounds
KR930007954A (en) Alkenyl cephalosporins and preparation methods thereof
KR930007955A (en) Pyridone alkenyl cephalosporins and preparation method thereof
AU1866388A (en) New process for the preparation of cephem compounds and new cephalosporin derivatives
KR870003107A (en) Method for preparing chianthine derivative
KR880012622A (en) Mannobiose derivatives
KR890002174A (en) Tricyclic Separm Compounds, Methods for Making and Uses thereof
KR840006667A (en) Method for preparing cephalosporin derivative
US3971780A (en) Thio-β-lactam cephalosporins
KR910000773A (en) 3-phenylthiosialic acid derivative, sialic acid containing oligosaccharide derivative, and its manufacturing method
KR850005441A (en) Method for preparing 3-alkoxy-2- (N-pyrrolidino) -N-pyridyl-N-furylmethyl (or furylthienyl) -propylamine
KR880000448A (en) Method for producing cephalosporin derivatives
US4039537A (en) Thio-β-lactam cephalosporins
KR920012021A (en) Method for preparing (S) -vinyl and -alenyl GABA
KR940021558A (en) Method for preparing a novel crystalline cephalosporin derivative
KR850000454A (en) Method for preparing cephalosporin derivative
US4018760A (en) Thio-β-lactam cephalosporins
KR940019713A (en) Method for preparing a novel cephalosporin derivative
EP0367036A3 (en) Substituted 3-aminosydnonimines, process for their preparation and their use
HUT47929A (en) Process for producing 4-piperidine-carboxamide derivatives and pharmaceuticals comprising same
KR960010653A (en) New cephalosporin antibiotics and preparation method thereof

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: 19970829

Year of fee payment: 6

LAPS Lapse due to unpaid annual fee