ES401525A1 - A procedure for the production of an antibiotic substance. (Machine-translation by Google Translate, not legally binding) - Google Patents

A procedure for the production of an antibiotic substance. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES401525A1
ES401525A1 ES401525A ES401525A ES401525A1 ES 401525 A1 ES401525 A1 ES 401525A1 ES 401525 A ES401525 A ES 401525A ES 401525 A ES401525 A ES 401525A ES 401525 A1 ES401525 A1 ES 401525A1
Authority
ES
Spain
Prior art keywords
group
aryloxy
aryl
alkyl
following general
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
ES401525A
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.)
Toyama Chemical Co Ltd
Original Assignee
Toyama Chemical Co Ltd
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
Priority claimed from JP2414171A external-priority patent/JPS5231879B1/ja
Priority claimed from JP2414071A external-priority patent/JPS531278B1/ja
Application filed by Toyama Chemical Co Ltd filed Critical Toyama Chemical Co Ltd
Publication of ES401525A1 publication Critical patent/ES401525A1/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • 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)
  • Cephalosporin Compounds (AREA)

Abstract

A procedure for the production of an antibiotic substance of the following general formula: **(See formula)** where Y represents (see formula) R represents a hydrogen atom, a halogen atom or an azido, acyloxy, alkoxy, aryloxy or SR'group (R' represents an alkyl, aryl or heterocyclic group), each of the radicals R1 and R2 represents a hydrogen atom or an alkyl, aryl, aralkyl, aryloxy, cycloalkane or heterocyclic group with or without substituents or R1 and R2 can form a ring together; R3 represents a hydrogen atom, a halogen atom or a hydroxyl, amino, alkylamino, azido, cyano, alkyloxy, alkylthio, aryloxycarbonyl, aralkyloxycarbonyl or alkoxycarbonyl group and n represents the integer 0 or 1; whose procedure consists in reacting the salts of 6-aminopenicilánica acid or 7-aminocefalosporónicos acids of the following general formula: **(See formula)** where the symbol Y has the meaning given above, with trivalent phosphorus compounds of the following general formula: **(See formula)** where R4 represents an alkyl, haloalkyl, aryl, aralkyl, alkyloxy, haloalkyloxy, aryloxy, aralkyloxy or dialkylamino group; R5 represents an alkyl, haloalkyl, aryl, aralkyl, alkyloxy, aryloxy, haloalkyloxy, aralkyloxy or dialkylamino group or a halogen atom or R4 and R5 can form a ring and X represents a halogen atom, reacting the product thus obtained with reactive derivatives of carboxylic acids of the following general formula: **(See formula)** where R1, R2, R3 and n have the meaning described above and then solvolize the product to remove the protecting group. (Machine-translation by Google Translate, not legally binding)
ES401525A 1971-04-15 1972-04-06 A procedure for the production of an antibiotic substance. (Machine-translation by Google Translate, not legally binding) Expired ES401525A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2414171A JPS5231879B1 (en) 1971-04-15 1971-04-15
JP2414071A JPS531278B1 (en) 1971-04-15 1971-04-15

Publications (1)

Publication Number Publication Date
ES401525A1 true ES401525A1 (en) 1975-09-01

Family

ID=26361623

Family Applications (1)

Application Number Title Priority Date Filing Date
ES401525A Expired ES401525A1 (en) 1971-04-15 1972-04-06 A procedure for the production of an antibiotic substance. (Machine-translation by Google Translate, not legally binding)

Country Status (19)

Country Link
AR (2) AR201419A1 (en)
AT (1) AT320849B (en)
BE (1) BE781934A (en)
BR (1) BR7202225D0 (en)
CA (1) CA1041996A (en)
CH (1) CH547309A (en)
CS (1) CS178106B2 (en)
DD (1) DD97422A5 (en)
DE (1) DE2218209C3 (en)
DK (1) DK142418B (en)
ES (1) ES401525A1 (en)
FR (1) FR2133686A1 (en)
HU (1) HU166324B (en)
IE (1) IE36288B1 (en)
IL (1) IL39062A (en)
NL (1) NL158803B (en)
NO (1) NO146986C (en)
PH (1) PH12645A (en)
SE (1) SE392275C (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE791099A (en) * 1971-11-09 1973-05-08 American Home Prod INTERMEDIARIES FOR THE PRODUCTION OF SEMI-SYNTHETIC PENICILLINS AND METHODS FOR OBTAINING THEM
GB1459999A (en) * 1972-12-27 1976-12-31 Novo Industri As Penicillin and cephalosporin intermediates
GB2161476B (en) 1984-05-25 1988-01-27 Toyama Chemical Co Ltd 2-aminothiazolyl-2-methoxyimino acetamides and their use in preparing cephalosporins

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE34822B1 (en) * 1969-12-26 1975-08-20 Univ Osaka Process for producing 6-amino penicillanic acid

Also Published As

Publication number Publication date
AR204077A1 (en) 1975-11-20
IE36288L (en) 1972-10-15
SE392275B (en) 1977-03-21
FR2133686A1 (en) 1972-12-01
NL7205083A (en) 1972-10-17
DE2218209C3 (en) 1980-10-16
IE36288B1 (en) 1976-09-29
AT320849B (en) 1975-02-25
CS178106B2 (en) 1977-08-31
FR2133686B1 (en) 1975-12-26
BR7202225D0 (en) 1973-07-17
NO146986B (en) 1982-10-04
DE2218209A1 (en) 1972-10-26
PH12645A (en) 1979-07-11
DK142418B (en) 1980-10-27
CA1041996A (en) 1978-11-07
DD97422A5 (en) 1973-05-05
SE392275C (en) 1983-11-28
AR201419A1 (en) 1975-03-14
NO146986C (en) 1983-01-12
DK142418C (en) 1982-12-06
CH547309A (en) 1974-03-29
BE781934A (en) 1972-10-11
IL39062A (en) 1975-02-10
IL39062A0 (en) 1972-05-30
NL158803B (en) 1978-12-15
HU166324B (en) 1975-02-28
DE2218209B2 (en) 1980-02-28

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