ES396389A1 - Procedure for the obtaining of acid compounds 7-acilamino-cef-3-em-4-carboxilico. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the obtaining of acid compounds 7-acilamino-cef-3-em-4-carboxilico. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES396389A1
ES396389A1 ES396389A ES396389A ES396389A1 ES 396389 A1 ES396389 A1 ES 396389A1 ES 396389 A ES396389 A ES 396389A ES 396389 A ES396389 A ES 396389A ES 396389 A1 ES396389 A1 ES 396389A1
Authority
ES
Spain
Prior art keywords
group
salt
formula
carboxyl group
compound
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
Application number
ES396389A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Ciba Geigy AG
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 Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of ES396389A1 publication Critical patent/ES396389A1/en
Expired 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
    • C07D501/08Preparation by forming the ring or condensed ring systems
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Procedure for obtaining 7-acylamino-cef-3-em-4-carboxylic acid compounds **(See formula)** wherein R1A signifies an Ac acyl group and R1b signifies hydrogen or a methylene moiety, optionally substituted, linked with an amino group existing in the position of the ac acyl moiety and R2 means hydrogen or an organic R2A moiety which together with the group -C (= O) -O- forms a protected carboxyl group, or the salts of such compounds with salt-forming groups, characterized in that in a compound of formula **(See formula)** or in a salt thereof, the free amino group is acylated to an Ac-NH group and, if desired, in a obtained compound, a protected carboxyl group of formula -C (= O) -O-R2A is transformed into the free carboxyl group or other protected carboxyl group of formula -C (= O) -O-R2A and/or, if desired, in a compound obtained, a free carboxyl group is transformed into a protected carboxyl group of formula -C (= O) -O-R2A and/or if desired, in a compound obtained the functional groups protected temporarily during the acylation reaction in the acyl moiety Ac are released and/or, if desired, a compound obtained with an amino group existing in the acyl residue Ac in the α position is reacted with an aldehyde or ketone and/or, if desired, a compound obtained with a salt-forming group is transformed into a salt or a salt obtained in the free compound or in another Salt. (Machine-translation by Google Translate, not legally binding)
ES396389A 1970-10-27 1971-10-26 Procedure for the obtaining of acid compounds 7-acilamino-cef-3-em-4-carboxilico. (Machine-translation by Google Translate, not legally binding) Expired ES396389A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH1584070A CH555859A (en) 1970-10-27 1970-10-27 8-oxo-7-amino-5-thia-1-azabicyclo (4,2,0) oct-2-ene compds - prepd fr 4-beta-(2ho-ethylthio)-1-alphaphosphoranylidene-protected carboxymeth

Publications (1)

Publication Number Publication Date
ES396389A1 true ES396389A1 (en) 1975-01-16

Family

ID=4412391

Family Applications (1)

Application Number Title Priority Date Filing Date
ES396389A Expired ES396389A1 (en) 1970-10-27 1971-10-26 Procedure for the obtaining of acid compounds 7-acilamino-cef-3-em-4-carboxilico. (Machine-translation by Google Translate, not legally binding)

Country Status (5)

Country Link
AU (1) AU472062B2 (en)
CH (1) CH555859A (en)
ES (1) ES396389A1 (en)
SU (2) SU468428A3 (en)
ZA (1) ZA716719B (en)

Also Published As

Publication number Publication date
SU468428A3 (en) 1975-04-25
ZA716719B (en) 1972-07-26
AU472062B2 (en) 1976-05-13
AU3493571A (en) 1973-05-03
SU460630A3 (en) 1975-02-15
CH555859A (en) 1974-11-15

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