KR970001531B1 - 화합물의 제조 방법 - Google Patents

화합물의 제조 방법 Download PDF

Info

Publication number
KR970001531B1
KR970001531B1 KR1019890005923A KR890005923A KR970001531B1 KR 970001531 B1 KR970001531 B1 KR 970001531B1 KR 1019890005923 A KR1019890005923 A KR 1019890005923A KR 890005923 A KR890005923 A KR 890005923A KR 970001531 B1 KR970001531 B1 KR 970001531B1
Authority
KR
South Korea
Prior art keywords
compound
formula
lower alkanoyl
isomer
solution
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Fee Related
Application number
KR1019890005923A
Other languages
English (en)
Korean (ko)
Other versions
KR890017256A (ko
Inventor
조지 그레이 마이클
그렉슨 마이클
Original Assignee
글락소 그룹 리미티드
비.에이.뉴샘
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 글락소 그룹 리미티드, 비.에이.뉴샘 filed Critical 글락소 그룹 리미티드
Publication of KR890017256A publication Critical patent/KR890017256A/ko
Application granted granted Critical
Publication of KR970001531B1 publication Critical patent/KR970001531B1/ko
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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
    • C07D501/02Preparation
    • 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
    • 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
    • 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
    • C07D501/34Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by carboxylic acids containing hetero rings

Landscapes

  • 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)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
KR1019890005923A 1988-05-03 1989-05-02 화합물의 제조 방법 Expired - Fee Related KR970001531B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB888810394A GB8810394D0 (en) 1988-05-03 1988-05-03 Chemical process
GB8810394.0 1988-05-03

Publications (2)

Publication Number Publication Date
KR890017256A KR890017256A (ko) 1989-12-15
KR970001531B1 true KR970001531B1 (ko) 1997-02-11

Family

ID=10636247

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019890005923A Expired - Fee Related KR970001531B1 (ko) 1988-05-03 1989-05-02 화합물의 제조 방법

Country Status (8)

Country Link
JP (1) JPH0256490A (enrdf_load_stackoverflow)
KR (1) KR970001531B1 (enrdf_load_stackoverflow)
CH (1) CH678856A5 (enrdf_load_stackoverflow)
DE (1) DE3914658A1 (enrdf_load_stackoverflow)
FR (1) FR2631031A1 (enrdf_load_stackoverflow)
GB (2) GB8810394D0 (enrdf_load_stackoverflow)
IT (1) IT1235502B (enrdf_load_stackoverflow)
NL (1) NL8901111A (enrdf_load_stackoverflow)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100187959B1 (ko) * 1997-03-31 1999-06-01 윤재승 저융점 무정형 세푸록심 악세틸의 제조방법
CN1111537C (zh) * 1997-05-15 2003-06-18 第一制糖株式会社 高纯晶形头孢呋辛1-乙酰氧乙酯的制备方法
IT1313569B1 (it) 1999-07-27 2002-09-09 Antibioticos Spa Processo per la sintesi di derivati beta-lattamici.

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1453049A (en) * 1973-08-21 1976-10-20 Glaxo Lab Ltd Cephalosporing antibiotics
US4011215A (en) * 1974-08-15 1977-03-08 Glaxo Laboratories Limited 3-Chloroalkylcarbamoyloxymethyl-7-[2-(fur-2-yl)-2-methoxyiminoacetamido]ceph-3-em-4-carboxylic acids and physiologically acceptable salts or oxides thereof
CA1094545A (en) * 1976-02-16 1981-01-27 Michael Gregson Cephalosporin antibiotics
GB2018764B (en) * 1978-04-07 1982-09-02 Glaxo Group Ltd Cephalosporin compounds
US4252974A (en) * 1978-04-07 1981-02-24 Glaxo Group Limited Cephalosporin compounds
GB2034312B (en) * 1978-09-21 1983-05-11 Glaxo Group Ltd Process for the preparation of cephalosporins
YU44680B (en) * 1982-07-30 1990-12-31 Glaxo Lab Ltd Process for obtaining very pure amorphous form of cephuroxim axetile
GB8320520D0 (en) * 1983-07-29 1983-09-01 Glaxo Group Ltd Chemical process
GB8400024D0 (en) * 1984-01-03 1984-02-08 Glaxo Group Ltd Cephalosporin antibiotics

Also Published As

Publication number Publication date
GB2218093A (en) 1989-11-08
GB8810394D0 (en) 1988-06-08
JPH0256490A (ja) 1990-02-26
IT8947902A0 (it) 1989-05-02
GB8909987D0 (en) 1989-06-21
DE3914658A1 (de) 1989-11-16
FR2631031A1 (fr) 1989-11-10
NL8901111A (nl) 1989-12-01
CH678856A5 (enrdf_load_stackoverflow) 1991-11-15
IT1235502B (it) 1992-09-05
KR890017256A (ko) 1989-12-15

Similar Documents

Publication Publication Date Title
US5693792A (en) β-lactam and cephem compounds and processes for their production
SE444811B (sv) Azetidinylforening for framstellning av 3-hydroxi-cefemforeningar och forfarande for dess framstellning
SE405857B (sv) Forfarande for substituerande av en grupp i 6-resp 7-stellning hos en penicillansyraforening eller cefalosporansyraforening
EP0118567B1 (en) Process for the preparationof 2-substituted cephem derivatives
KR970001531B1 (ko) 화합물의 제조 방법
US4122086A (en) Isopenicillins
EP1132391B1 (en) Process for the preparation of 3-sulfonyloxy-3-cephem compounds
JPH0686459B2 (ja) 3―置換チオ―3―セフエム化合物の製造法
EP0117872B1 (en) Process for preparing cephalosporin compounds
US4012381A (en) Process for preparing cephalosporins and intermediates
US3941779A (en) Method for producing 2-(substituted thio)-3-cephem derivatives
US4160091A (en) Process for preparation of 3-halo-3-methylcephams
EP0153874A2 (en) Cephalosporin intermediates and their preparation
KR970001530B1 (ko) 화합물의 제조 방법
US4959495A (en) Process for the preparation of intermediates used to produce aminothiazoloximino cephalosporins
KR920005969B1 (ko) 세팔로스포린 화합물의 제조방법
US4485235A (en) Process for preparing 7-α-methoxycephem compounds
KR900006810B1 (ko) 세푸록심 및 그 중간체의 제조 방법
JP2669955B2 (ja) アゼチジノン誘導体及びその製造法
EP0120094B1 (en) Azetidinone compounds
JP3227497B2 (ja) β−ラクタム化合物及びその製造法
PL83186B1 (en) 3-halomethyl-d*su3-cephalosporin esters and sulfoxides thereo f useful in the production of antibiotics, and process for preparing the new intermediates and antibiotics[ca986094a]
CA1133470A (en) Cephapirine esters, salts thereof and processes for producing the same
KR960011777B1 (ko) 신규한 결정성 세팔로스포린 유도체 및 그의 제조방법
EP0759428A1 (en) Process for the production of beta-lactam compounds

Legal Events

Date Code Title Description
PA0109 Patent application

St.27 status event code: A-0-1-A10-A12-nap-PA0109

R17-X000 Change to representative recorded

St.27 status event code: A-3-3-R10-R17-oth-X000

PG1501 Laying open of application

St.27 status event code: A-1-1-Q10-Q12-nap-PG1501

A201 Request for examination
P11-X000 Amendment of application requested

St.27 status event code: A-2-2-P10-P11-nap-X000

P13-X000 Application amended

St.27 status event code: A-2-2-P10-P13-nap-X000

PA0201 Request for examination

St.27 status event code: A-1-2-D10-D11-exm-PA0201

E902 Notification of reason for refusal
PE0902 Notice of grounds for rejection

St.27 status event code: A-1-2-D10-D21-exm-PE0902

P11-X000 Amendment of application requested

St.27 status event code: A-2-2-P10-P11-nap-X000

P13-X000 Application amended

St.27 status event code: A-2-2-P10-P13-nap-X000

G160 Decision to publish patent application
PG1605 Publication of application before grant of patent

St.27 status event code: A-2-2-Q10-Q13-nap-PG1605

E701 Decision to grant or registration of patent right
PE0701 Decision of registration

St.27 status event code: A-1-2-D10-D22-exm-PE0701

GRNT Written decision to grant
PR0701 Registration of establishment

St.27 status event code: A-2-4-F10-F11-exm-PR0701

PR1002 Payment of registration fee

St.27 status event code: A-2-2-U10-U11-oth-PR1002

Fee payment year number: 1

PN2301 Change of applicant

St.27 status event code: A-5-5-R10-R13-asn-PN2301

St.27 status event code: A-5-5-R10-R11-asn-PN2301

PR1001 Payment of annual fee

St.27 status event code: A-4-4-U10-U11-oth-PR1001

Fee payment year number: 4

FPAY Annual fee payment

Payment date: 20010201

Year of fee payment: 5

PR1001 Payment of annual fee

St.27 status event code: A-4-4-U10-U11-oth-PR1001

Fee payment year number: 5

LAPS Lapse due to unpaid annual fee
PC1903 Unpaid annual fee

St.27 status event code: A-4-4-U10-U13-oth-PC1903

Not in force date: 20020212

Payment event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE

PC1903 Unpaid annual fee

St.27 status event code: N-4-6-H10-H13-oth-PC1903

Ip right cessation event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE

Not in force date: 20020212

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000

R18-X000 Changes to party contact information recorded

St.27 status event code: A-5-5-R10-R18-oth-X000