GB1293590A - New penicillanic acid derivatives - Google Patents

New penicillanic acid derivatives

Info

Publication number
GB1293590A
GB1293590A GB33211/70A GB3321170A GB1293590A GB 1293590 A GB1293590 A GB 1293590A GB 33211/70 A GB33211/70 A GB 33211/70A GB 3321170 A GB3321170 A GB 3321170A GB 1293590 A GB1293590 A GB 1293590A
Authority
GB
United Kingdom
Prior art keywords
radical
reacting
formula
amide
substituted
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
GB33211/70A
Inventor
Frantz Johannes Lund
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.)
Leo Pharma AS
Original Assignee
Leo Pharmaceutical Products Ltd AS
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 to BE758782D priority Critical patent/BE758782A/en
Application filed by Leo Pharmaceutical Products Ltd AS filed Critical Leo Pharmaceutical Products Ltd AS
Priority to IL35490A priority patent/IL35490A/en
Priority to IE1359/70A priority patent/IE34620B1/en
Priority to CH1644070A priority patent/CH559752A5/xx
Priority to AT995970A priority patent/AT301026B/en
Priority to CH1113074A priority patent/CH559753A5/xx
Priority to DK565070AA priority patent/DK135127B/en
Priority to SU1489793A priority patent/SU406362A3/ru
Priority to RO72470A priority patent/RO60563A/ro
Priority to CS7560A priority patent/CS166020B2/cs
Priority to FR7040428A priority patent/FR2073338A1/en
Priority to PL1970144350A priority patent/PL90581B1/en
Priority to IT70739/70A priority patent/IT1044209B/en
Priority to NLAANVRAGE7016435,A priority patent/NL168227C/en
Priority to NO4290/70A priority patent/NO137826C/en
Priority to LU62031D priority patent/LU62031A1/xx
Priority to SE7015181A priority patent/SE397355B/en
Priority to RO64921A priority patent/RO56878A/ro
Priority to YU275370A priority patent/YU36522B/en
Priority to JP45099009A priority patent/JPS518955B1/ja
Priority to HULO372A priority patent/HU162440B/hu
Priority to BG1880370A priority patent/BG18189A3/xx
Priority to BG16025A priority patent/BG18619A3/xx
Priority to ES385437A priority patent/ES385437A1/en
Priority to DE2055531A priority patent/DE2055531C3/en
Priority to FI3032/70A priority patent/FI54601C/en
Publication of GB1293590A publication Critical patent/GB1293590A/en
Priority to US05/303,715 priority patent/US3957764A/en
Priority to YU240378A priority patent/YU36523B/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C259/00Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
    • C07C259/02Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by halogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

1293590 Amidino-penicillanic acids LOVENS KEMISKE FABRIK PRODUKTIONSAK TIESELSKAB 10 Nov 1970 [11 Nov 1969 8 July 1970] 55209/69 and 33211/70 Headings C2A and C2C Novel amidino-penicillanic acid derivatives of Formula I: and salts thereof, wherein R<SP>1</SP> and R<SP>2</SP> each represent an aliphatic hydrocarbon radical, a mono- or bi-cyclic aryl radical, a cycloalkyl radical, a cycloalkyl-alkyl radical, a heterocyclic radical or a heterocyclically substituted alkyl radical, which radicals may be substituted, e.g. by one or more halogen atoms or alkyl, hydroxy, alkoxy, alkylthio, acyl, carboxy, carbalkoxy, carbamyl, carbamido, cyano, sulphonyl, amino or substituted amino radicals, or R<SP>1</SP> and R<SP>2</SP> together with the common nitrogen atom form a ring system, and R<SP>3</SP> is hydroxyl or substituted hydroxyl, are prepared by either (a) reacting a reactive derivative of an amide or thioamide of formula where R<SP>5</SP> is oxygen or sulphur, with a 6-aminopenicillanic acid ester, or (b) reacting an amine of formula R<SP>1</SP>R<SP>2</SP>NH with a reactive derivative of a 6-formamidopenicillanic acid ester, and, if required, subsequently hydrolysing the ester group. Reactive derivatives of the amides may be the amide halide, the amide dialkyl sulphate complex or the amide acetal; the thioamides are used as a thioamide alkyl halide complex. The 6-formamidopenicillanic acid ester reactive derivative is preferably obtained by reacting 6-APA with a 1,1-dihalodimethyl ether. Chloral is reacted with each of the following: hexamethylene-imine, formamide, and #-N- butylaminopropionitrile to give respectively: N - formylhexamethyleneimine, N - ethyl - N - #- ethoxyethylformamide and N - butyl - # - formamidopropionitrile. The said compounds are each treated with oxalyl chloride to give the corresponding chloroformiminium chlorides. Chloro - (methyl - carbomethoxymethyl) - formiminium chloride is obtained by treating methyl N-formyl-N-methylglycinate with phosgene. A methyl iodide complex of N-thioformylhexamethyleneimine is prepared by reacting these component compounds. N - Formylhexamethyleneimine - dimethyl sulphate complex is analogously prepared, and is reacted with sodium methoxide to form 1-hexamethyleneiminecarboxaldehyde-dimethyl acetal. Pharmaceutical compositions having antibiotic activity against gram-negative bacteria comprise a penicillanic-acid of Formula I as defined above or a pharmaceutically acceptable salt thereof or an ester thereof which is hydrolysable in the human body, together with a pharmaceutical carrier.
GB33211/70A 1969-11-11 1969-11-11 New penicillanic acid derivatives Expired GB1293590A (en)

Priority Applications (28)

Application Number Priority Date Filing Date Title
BE758782D BE758782A (en) 1969-11-11 NEW DERIVATIVES OF 6-AMIDINO PENICILLANIC ACID, THEIR PREPARATION PROCESS AND THEIR APPLICATIONS AS ANTIBIOTICS
IL35490A IL35490A (en) 1969-11-11 1970-10-20 6-amidino-penicillanic acid derivatives,their preparation and pharmaceutical compositions containing them
IE1359/70A IE34620B1 (en) 1969-11-11 1970-10-22 New penicillanic acid derivatives
CH1644070A CH559752A5 (en) 1969-11-11 1970-11-05
AT995970A AT301026B (en) 1969-11-11 1970-11-05 Process for the preparation of new aminopenicillanic acid derivatives
CH1113074A CH559753A5 (en) 1969-11-11 1970-11-05
DK565070AA DK135127B (en) 1969-11-11 1970-11-06 Analogous process for the preparation of derivatives of 6-aminopenicillanic acid.
SU1489793A SU406362A3 (en) 1969-11-11 1970-11-09
NLAANVRAGE7016435,A NL168227C (en) 1969-11-11 1970-11-10 METHOD FOR PREPARING A MEDICINAL PRODUCT WITH ANTIBIOTIC ACTIVITY, AND METHOD FOR PREPARING A DERIVATIVE OF 6-AMINOPENICILLANIC ACID
CS7560A CS166020B2 (en) 1969-11-11 1970-11-10
FR7040428A FR2073338A1 (en) 1969-11-11 1970-11-10 6-(methyleneamino)-penicillanic acid derivs
PL1970144350A PL90581B1 (en) 1969-11-11 1970-11-10 6-(methyleneamino)-penicillanic acid derivs[FR2073338A1]
IT70739/70A IT1044209B (en) 1969-11-11 1970-11-10 PROCEDURE FOR THE PREPARATION OF PENICILLANIC ACID DERIVATIVES
RO72470A RO60563A (en) 1969-11-11 1970-11-10
NO4290/70A NO137826C (en) 1969-11-11 1970-11-10 ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY EFFECTIVE DERIVATIVES OF 6-AMINO-PENICILLANIC ACID
LU62031D LU62031A1 (en) 1969-11-11 1970-11-10
SE7015181A SE397355B (en) 1969-11-11 1970-11-10 ANALOGICAL PROCEDURE FOR PREPARING NEW PENICILLANIC ACID DERIVATIVES
RO64921A RO56878A (en) 1969-11-11 1970-11-10
YU275370A YU36522B (en) 1969-11-11 1970-11-10 Process for obtaining new penicillanic acid derivatives
JP45099009A JPS518955B1 (en) 1969-11-11 1970-11-11
HULO372A HU162440B (en) 1969-11-11 1970-11-11
BG1880370A BG18189A3 (en) 1970-07-08 1970-11-11
BG16025A BG18619A3 (en) 1969-11-11 1970-11-11
ES385437A ES385437A1 (en) 1969-11-11 1970-11-11 Method for the preparation of new derivatives of penicilanico acid. (Machine-translation by Google Translate, not legally binding)
DE2055531A DE2055531C3 (en) 1969-11-11 1970-11-11 Amidinopenicillanic acid derivatives, processes for the preparation of these compounds and their use in combating infectious diseases
FI3032/70A FI54601C (en) 1969-11-11 1970-11-11 FOERFARANDE FOER FRAMSTAELLNING AV TERAPEUTISKT VERKSAMMA 6-AMIDINOPENICILLANSYRADERIVAT
US05/303,715 US3957764A (en) 1969-11-11 1972-11-06 6-aminopenicillanic acid derivatives
YU240378A YU36523B (en) 1969-11-11 1978-10-13 Process for obtaining new penicillanic acid derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB5520969 1969-11-11

Publications (1)

Publication Number Publication Date
GB1293590A true GB1293590A (en) 1972-10-18

Family

ID=10473274

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33211/70A Expired GB1293590A (en) 1969-11-11 1969-11-11 New penicillanic acid derivatives

Country Status (4)

Country Link
CY (1) CY823A (en)
GB (1) GB1293590A (en)
MY (1) MY7500250A (en)
ZA (1) ZA707347B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2404587A1 (en) * 1973-02-02 1974-08-15 Leo Pharm Prod Ltd PROCESS FOR THE PREPARATION OF 6-AMINOPENICILLANEUR DERIVATEN
US4089963A (en) * 1972-03-13 1978-05-16 Astra Pharmaceutical Products, Inc. Esters of amidinopenicillanic acids, pharmaceutical preparations and method for treating infectious diseases
US4557932A (en) * 1982-02-02 1985-12-10 Leo Pharmaceutical Products Ltd. Antibacterial synergistic pharmaceutical compositions
EP0187626A1 (en) * 1984-11-09 1986-07-16 Astra Läkemedel Aktiebolag Stabilized bacampicillin hydrochloride, process for the stabilization and pharmaceutical compositions
CN114573603A (en) * 2022-03-07 2022-06-03 南京美智德合成材料有限公司 Process for synthesizing pimecrcillin in one pot

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4089963A (en) * 1972-03-13 1978-05-16 Astra Pharmaceutical Products, Inc. Esters of amidinopenicillanic acids, pharmaceutical preparations and method for treating infectious diseases
DE2404587A1 (en) * 1973-02-02 1974-08-15 Leo Pharm Prod Ltd PROCESS FOR THE PREPARATION OF 6-AMINOPENICILLANEUR DERIVATEN
US4557932A (en) * 1982-02-02 1985-12-10 Leo Pharmaceutical Products Ltd. Antibacterial synergistic pharmaceutical compositions
EP0187626A1 (en) * 1984-11-09 1986-07-16 Astra Läkemedel Aktiebolag Stabilized bacampicillin hydrochloride, process for the stabilization and pharmaceutical compositions
US4626532A (en) * 1984-11-09 1986-12-02 Astra Lakemedel Aktieboag Process for stabilization of bacampicillin hydrochloride
CN114573603A (en) * 2022-03-07 2022-06-03 南京美智德合成材料有限公司 Process for synthesizing pimecrcillin in one pot

Also Published As

Publication number Publication date
ZA707347B (en) 1971-09-29
CY823A (en) 1976-03-19
MY7500250A (en) 1975-12-31

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Legal Events

Date Code Title Description
PS Patent sealed
PE20 Patent expired after termination of 20 years