ES391532A1 - Procedure for the obtaining of penicillines. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the obtaining of penicillines. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES391532A1
ES391532A1 ES391532A ES391532A ES391532A1 ES 391532 A1 ES391532 A1 ES 391532A1 ES 391532 A ES391532 A ES 391532A ES 391532 A ES391532 A ES 391532A ES 391532 A1 ES391532 A1 ES 391532A1
Authority
ES
Spain
Prior art keywords
compounds
formula
see formula
general
general formulas
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
ES391532A
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.)
Bayer AG
Original Assignee
Bayer 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
Priority claimed from DE2025414A external-priority patent/DE2025414C3/en
Priority claimed from DE19712104580 external-priority patent/DE2104580C3/en
Application filed by Bayer AG filed Critical Bayer AG
Publication of ES391532A1 publication Critical patent/ES391532A1/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
    • C07D499/21Heterocyclic 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 with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
    • C07D499/44Compounds with an amino radical acylated by carboxylic acids, attached in position 6
    • C07D499/48Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical
    • C07D499/58Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical
    • C07D499/64Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical by nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/429Thiazoles condensed with heterocyclic ring systems
    • A61K31/43Compounds 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/30Oxygen or sulfur atoms
    • C07D233/32One oxygen atom
    • C07D233/38One oxygen atom with acyl radicals or hetero atoms directly attached to ring nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/68Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • 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
    • C07D499/21Heterocyclic 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 with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
    • C07D499/44Compounds with an amino radical acylated by carboxylic acids, attached in position 6
    • C07D499/48Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical
    • C07D499/58Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical
    • C07D499/64Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical by nitrogen atoms
    • C07D499/68Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical by nitrogen atoms with aromatic rings as additional substituents on the carbon chain

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Medicinal Chemistry (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)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Procedure for obtaining penicillins, of general formula I: **(See formula)** whose compounds, as for the center of chirality Cx; they can be presented in the two possible configurations R and S and as mixtures of the resulting diastereomers, as well as the pharmaceutically tolerable non-toxic salts of these compounds; characterized in that a compound chosen from the compounds of general formula II **(See formula)** condensation products of compounds of general formula II with carbonyl compounds, such as acetone, of general formula III **(See formula)** and compounds of general formulas IV and V **(See formula)** (see formula) they are reacted with a compound chosen from the compounds of general formulas VI, VII and VIII **(See formula)** in which W represents halogen or asido, in the case of using the compounds of the general formulas II and III, in anhydrous or aqueous solvents, in the presence of a base and, in the case of using the compounds of the general formulas IV and V, in anhydrous and hydroxyl group-free solvents, with or without addition of a base, at a temperature between -20º and + 50ºC. (Machine-translation by Google Translate, not legally binding)
ES391532A 1970-05-25 1971-05-25 Procedure for the obtaining of penicillines. (Machine-translation by Google Translate, not legally binding) Expired ES391532A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2025414A DE2025414C3 (en) 1970-05-25 1970-05-25 Cyclic acylureidophenylacetamidopenicillanic acids
DE19712104580 DE2104580C3 (en) 1971-02-01 1971-02-01 Acylureidopenicillins

Publications (1)

Publication Number Publication Date
ES391532A1 true ES391532A1 (en) 1974-10-01

Family

ID=25759178

Family Applications (4)

Application Number Title Priority Date Filing Date
ES391532A Expired ES391532A1 (en) 1970-05-25 1971-05-25 Procedure for the obtaining of penicillines. (Machine-translation by Google Translate, not legally binding)
ES403125A Expired ES403125A1 (en) 1970-05-25 1972-05-24 Procedure for obtaining an antibacterial composition. (Machine-translation by Google Translate, not legally binding)
ES403124A Expired ES403124A1 (en) 1970-05-25 1972-05-24 Procedure for obtaining an antibacterial composition. (Machine-translation by Google Translate, not legally binding)
ES403126A Expired ES403126A1 (en) 1970-05-25 1972-05-24 Procedure for obtaining an antibacterial composition. (Machine-translation by Google Translate, not legally binding)

Family Applications After (3)

Application Number Title Priority Date Filing Date
ES403125A Expired ES403125A1 (en) 1970-05-25 1972-05-24 Procedure for obtaining an antibacterial composition. (Machine-translation by Google Translate, not legally binding)
ES403124A Expired ES403124A1 (en) 1970-05-25 1972-05-24 Procedure for obtaining an antibacterial composition. (Machine-translation by Google Translate, not legally binding)
ES403126A Expired ES403126A1 (en) 1970-05-25 1972-05-24 Procedure for obtaining an antibacterial composition. (Machine-translation by Google Translate, not legally binding)

Country Status (28)

Country Link
JP (1) JPS5538357B1 (en)
AR (2) AR195267A1 (en)
AT (1) AT307617B (en)
BE (1) BE767647A (en)
BG (1) BG23220A3 (en)
CA (1) CA943128A (en)
CH (1) CH562249A5 (en)
CS (1) CS171230B2 (en)
CY (1) CY829A (en)
DD (1) DD91497B3 (en)
DK (1) DK133679C (en)
EG (1) EG10856A (en)
ES (4) ES391532A1 (en)
FI (1) FI54484C (en)
FR (1) FR2100681B1 (en)
GB (1) GB1301961A (en)
HU (1) HU162205B (en)
IE (1) IE35311B1 (en)
IL (1) IL36905A (en)
KE (1) KE2592A (en)
LU (1) LU63203A1 (en)
NL (1) NL172660C (en)
NO (1) NO141164C (en)
PH (1) PH14794A (en)
RO (2) RO62689A (en)
SE (1) SE395896B (en)
SU (1) SU472507A3 (en)
YU (1) YU130271A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2354219A1 (en) * 1973-10-30 1975-05-07 Bayer Ag BETA-LACTAM-ANTIBIOTICA, A PROCESS FOR THEIR MANUFACTURING AND ITS USE AS A MEDICINAL PRODUCT
US4039673A (en) 1973-10-30 1977-08-02 Bayer Aktiengesellschaft Penicillins and cephalosporins and their production
GB1486349A (en) * 1974-11-28 1977-09-21 Bayer Ag Beta-lactam antibiotics process for their preparation and their use as medicaments
GB1584400A (en) * 1976-12-24 1981-02-11 Bayer Ag (2-oxo-imidazoliden-1-yl(carbonylamino)-acetamido-cephalosporins and penicillins
DE2658906A1 (en) * 1976-12-24 1978-07-06 Bayer Ag BETA-LACTAM ANTIBIOTICS, THE METHOD OF MANUFACTURING AND THEIR USE AS A MEDICINAL PRODUCT
CA1133896A (en) * 1978-05-26 1982-10-19 Nobuhiro Oi Penicillanic acid derivative and process for preparing the same
JPS5732289A (en) 1980-08-05 1982-02-20 Chugai Pharmaceut Co Ltd Alpha-substituted ureidobenzylpenicillin

Also Published As

Publication number Publication date
AR195267A1 (en) 1973-09-28
KE2592A (en) 1976-01-09
CA943128A (en) 1974-03-05
ES403125A1 (en) 1975-12-16
DD91497B3 (en) 1988-01-27
NO141164C (en) 1980-01-23
CH562249A5 (en) 1975-05-30
BG23220A3 (en) 1977-07-12
FR2100681A1 (en) 1972-03-24
DD91497A5 (en) 1972-07-20
CS171230B2 (en) 1976-10-29
DK133679C (en) 1976-11-15
IE35311L (en) 1971-11-25
BE767647A (en) 1971-11-25
RO62689A (en) 1978-05-15
RO59157A (en) 1976-04-15
NL172660B (en) 1983-05-02
FI54484C (en) 1978-12-11
DK133679B (en) 1976-06-28
SU472507A3 (en) 1975-05-30
NL172660C (en) 1983-10-03
EG10856A (en) 1977-05-31
JPS5538357B1 (en) 1980-10-03
FR2100681B1 (en) 1974-10-18
YU130271A (en) 1982-02-25
NL7107175A (en) 1971-11-29
AR195946A1 (en) 1973-11-15
AT307617B (en) 1973-05-25
ES403124A1 (en) 1976-01-01
CY829A (en) 1976-03-19
PH14794A (en) 1981-12-09
ES403126A1 (en) 1975-05-01
FI54484B (en) 1978-08-31
IL36905A0 (en) 1971-07-28
NO141164B (en) 1979-10-15
IE35311B1 (en) 1976-01-07
IL36905A (en) 1975-11-25
HU162205B (en) 1973-01-29
SE395896B (en) 1977-08-29
LU63203A1 (en) 1971-09-01
GB1301961A (en) 1973-01-04

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 19910215