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AR050958A1 - BICYCLE ANTIBIOTICS - Google Patents

BICYCLE ANTIBIOTICS

Info

Publication number
AR050958A1
AR050958A1 ARP050104029A ARP050104029A AR050958A1 AR 050958 A1 AR050958 A1 AR 050958A1 AR P050104029 A ARP050104029 A AR P050104029A AR P050104029 A ARP050104029 A AR P050104029A AR 050958 A1 AR050958 A1 AR 050958A1
Authority
AR
Argentina
Prior art keywords
ch2ch2
ch2ch
nhco
alkyl
och2
Prior art date
Application number
ARP050104029A
Other languages
Spanish (es)
Original Assignee
Actelion Percurex 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 Actelion Percurex Ag filed Critical Actelion Percurex Ag
Publication of AR050958A1 publication Critical patent/AR050958A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Quinoline Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Reivindicacion 1: Un compuesto seleccionado desde el grupo consistente de un compuesto de la formula (1) donde R1 representa un alquil, alcoxi, haloalcoxi, halogeno o ciano; uno o dos de U, V, W y X representa(n) N, el resto representa CH, o, en el caso de U, V y/o W, puede también representar CRa y, en el caso de X, puede también representar CRb; Ra representa halogeno; Rb representa un halogeno o alcoxi; D representa un alquil, aril o heteroaril; M es seleccionado desde el grupo consistente de M1, M2, M3 y M4; M1 donde A1 representa NHCO, OCH2, CH2CH2, CH=CH o CH(OH)CH2; A2 representa NHCH2, NHCO, NHCH2CONH, NHCH2CH=CH, CH2CH2, CH2CO, COCH2, CH2CH(OH) o CH2CH(OCONH2); B1 y B2 cada uno representa independientemente cada uno del otro N o CH; cuando A1 representa OCH2, B1 representa CH; n es 1; o n es también 0 cuando B1 es CH; y p es 1; o p es también 0 cuando B2 es CH; M2 donde A3 representa NHCO, CH2CH2, CH=CH, COCH2, CH(OH)CH2, CH2CH(OH), CH(OH)CH(OH) o OCH2; A4 representa CH2, CO, CH2CH=CH, COCH=CH o CH2CONH; R2 representa H, alquil, hidroxialquil, alquilcarboniloxialquil, carbamoiloxialquil, carboxialquil o carbamoilalquil; R3 y R4 cada uno independientemente representa H, hidroxi o alquilcarboniloxi; o R3 y R4 juntos representan union de cadena dimetilmetilenodioxi unida a carbonos de apoyo de carbonos de R3 y R4; R5 representa H alquil o hidroxialquil; y la doble línea representa un enlace simple o, cuando R3 y r4 representan H, también representa un doble enlace; M3 donde A5 representa CH2CH2, CH=CH, COCH2, CH(OH)CH2, NHCO(CH2)m, NHCOCH2O, NHCOOCH2 o O(CH2)q; m es 0, 1 o 2; q es 1, 2 o 3 y B6 representa N y A6 representa CH2, CH2CH2, CH2CH=CH o CH2CH2S; o B6 representa CH y A6 representa CH2NHCH2, CH2NHCH2CONH o CH2NHCH2CH=CH; M4 donde A7 representa NHCO, CH2CH2 o OCH2; A8 representa CH2; y R6 representa H o alquil; y una prodroga, un tautomero, un enantiomero optimamente puro, una mezcla de enantiomeros, un racemato, un diastereoisomero optimamente puro, una mezcla de diastereoisomeros, un racemato diastereoisomérico, mezcla de racematos diastereoisoméricos, una meso-forma, una forma morfologica, una sal o un complejo solvente de tal compuesto.Claim 1: A compound selected from the group consisting of a compound of the formula (1) wherein R 1 represents an alkyl, alkoxy, haloalkoxy, halogen or cyano; one or two of U, V, W and X represents (n) N, the rest represents CH, or, in the case of U, V and / or W, may also represent CRa and, in the case of X, may also represent CRb; Ra represents halogen; Rb represents a halogen or alkoxy; D represents an alkyl, aryl or heteroaryl; M is selected from the group consisting of M1, M2, M3 and M4; M1 where A1 represents NHCO, OCH2, CH2CH2, CH = CH or CH (OH) CH2; A2 represents NHCH2, NHCO, NHCH2CONH, NHCH2CH = CH, CH2CH2, CH2CO, COCH2, CH2CH (OH) or CH2CH (OCONH2); B1 and B2 each independently represents each other's N or CH; when A1 represents OCH2, B1 represents CH; n is 1; or n is also 0 when B1 is CH; and p is 1; or p is also 0 when B2 is CH; M2 where A3 represents NHCO, CH2CH2, CH = CH, COCH2, CH (OH) CH2, CH2CH (OH), CH (OH) CH (OH) or OCH2; A4 represents CH2, CO, CH2CH = CH, COCH = CH or CH2CONH; R2 represents H, alkyl, hydroxyalkyl, alkylcarbonyloxyalkyl, carbamoyloxyalkyl, carboxyalkyl or carbamoylalkyl; R3 and R4 each independently represents H, hydroxy or alkylcarbonyloxy; or R3 and R4 together represent dimethylmethylenedioxy chain bonding to carbon support carbons of R3 and R4; R5 represents H alkyl or hydroxyalkyl; and the double line represents a single bond or, when R3 and r4 represent H, it also represents a double bond; M3 where A5 represents CH2CH2, CH = CH, COCH2, CH (OH) CH2, NHCO (CH2) m, NHCOCH2O, NHCOOCH2 or O (CH2) q; m is 0, 1 or 2; q is 1, 2 or 3 and B6 represents N and A6 represents CH2, CH2CH2, CH2CH = CH or CH2CH2S; or B6 represents CH and A6 represents CH2NHCH2, CH2NHCH2CONH or CH2NHCH2CH = CH; M4 where A7 represents NHCO, CH2CH2 or OCH2; A8 represents CH2; and R6 represents H or alkyl; and a prodrug, a tautomer, an optimally pure enantiomer, a mixture of enantiomers, a racemate, an optimally pure diastereoisomer, a mixture of diastereoisomers, a diastereoisomeric racemate, mixture of diastereoisomeric racemates, a meso-form, a morphological form, a salt or a solvent complex of such a compound.

ARP050104029A 2004-09-24 2005-09-26 BICYCLE ANTIBIOTICS AR050958A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP2004010762 2004-09-24
EP2005007731 2005-07-15

Publications (1)

Publication Number Publication Date
AR050958A1 true AR050958A1 (en) 2006-12-06

Family

ID=36090370

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP050104029A AR050958A1 (en) 2004-09-24 2005-09-26 BICYCLE ANTIBIOTICS

Country Status (5)

Country Link
JP (1) JP4887297B2 (en)
AR (1) AR050958A1 (en)
CA (1) CA2580621A1 (en)
TW (1) TW200615267A (en)
WO (1) WO2006032466A2 (en)

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EP1987040B1 (en) 2006-02-15 2010-11-10 Actelion Pharmaceuticals Ltd. Ethanol or 1,2-ethanediol cyclohexyl antibiotic derivatives
CA2643962A1 (en) * 2006-03-10 2007-09-20 Actelion Pharmaceuticals Ltd Antibiotic compounds
WO2007115947A1 (en) 2006-04-06 2007-10-18 Glaxo Group Limited Pyrrolo-quinoxalinone derivatives as antibacterials
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EP1992628A1 (en) 2007-05-18 2008-11-19 Glaxo Group Limited Derivatives and analogs of N-ethylquinolones and N-ethylazaquinolones
TW200819457A (en) 2006-08-30 2008-05-01 Actelion Pharmaceuticals Ltd Spiro antibiotic derivatives
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Also Published As

Publication number Publication date
JP4887297B2 (en) 2012-02-29
WO2006032466A2 (en) 2006-03-30
JP2008514563A (en) 2008-05-08
WO2006032466A3 (en) 2006-12-14
CA2580621A1 (en) 2006-03-30
TW200615267A (en) 2006-05-16

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