AR053683A1 - Derivados de piperidina con actividad antibacteriana - Google Patents

Derivados de piperidina con actividad antibacteriana

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Publication number
AR053683A1
AR053683A1 ARP060100590A ARP060100590A AR053683A1 AR 053683 A1 AR053683 A1 AR 053683A1 AR P060100590 A ARP060100590 A AR P060100590A AR P060100590 A ARP060100590 A AR P060100590A AR 053683 A1 AR053683 A1 AR 053683A1
Authority
AR
Argentina
Prior art keywords
alkyl
carbamoyl
halo
alkoxy
alkanoyl
Prior art date
Application number
ARP060100590A
Other languages
English (en)
Inventor
G Basarab
B Dangel
P Fleming
Michael Gravestock
O Green
Sheila Hauck
P Hill
K Hull
G Mullen
B Sherer
Fel Zhou
Original Assignee
Astrazeneca Ab
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=36218455&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR053683(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR053683A1 publication Critical patent/AR053683A1/es

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Classifications

    • 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
    • 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
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541Non-condensed thiazines containing further heterocyclic rings
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • 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)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

Compuestos de formula (1) y sus sales aceptables para uso farmacéutico. Procesos para su preparacion, composiciones farmacéuticas que los contienen, su uso como medicamentos y su uso en el tratamiento de infecciones bacterianas. Reivindicacion 1: Un compuesto caracterizado porque responde a la formula (1), en donde: R1 se selecciona entre hidrogeno, nitro, hidroxi, halo, ciano, alquilo C1-4, alcoxi C1-4, alquenilo C2-4, alquinilo C2-4, alcanoilo C1-4, alquilC1-4S(O)a, en donde a es entre 0 y 2 y cicloalquilo C3-6; en donde R1 puede estar opcionalmente sustituido sobre carbono por uno o más halo o ciclopropilo; R2 se selecciona entre hidrogeno, nitro, hidroxi, halo, ciano, alquilo C1-4, alcoxi C1-4, alquenilo C2-4, alquinilo C2-4, alcanoilo C1-4, alquilC1-4S(O)a, en donde a es entre 0 y 2 y cicloalquilo C3-6; en donde R2 puede estar opcionalmente sustituido sobre carbono por uno o más halo o cicloalquilo C3-6; R3 se selecciona entre hidrogeno, nitro, hidroxi, halo, ciano, - C=N-OR', en donde R' es H o alquilo C1-4, alquilo C1-4, alcoxi C1-4, alquenilo C2-4, alquinilo C2-4, alcanoilo C1-4, alquilC1-4S(O)a, en donde a es entre 0 y 2 y cicloalquilo C3-6; en donde R3 puede estar opcionalmente sustituido sobre carbono por uno o más halo o cicloalquilo C3-6; W es -O-, -N(R6)- o -C(R7)(R8)-; X es un enlace directo, -CH2-, -C(O)- o -S(O)q- (en donde q es 1 o 2); el anillo A es carbociclilo o heterociclilo; en donde si dicho heterociclilo contiene una porcion -NH- dicho nitrogeno puede estar opcionalmente sustituido por un grupo seleccionado entre R9; R4 y R5 son sustituyentes sobre carbono y se seleccionan en forma independiente entre halo, nitro, ciano, hidroxi, trifluorometoxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, sulfo, formilo, ureido, hidroxiiminometilo, alcoxiiminometilo C1-4, N-hidroxiformanido, hidrazino C1-4, hidrazinocarbonilo, N-hidroxiethanimidoilo, amino(hidroxiimino)metilo, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, alcoxi C1-4, alcanoilo C1-4, alcanoiloxi C1-4, N-(alquilC1-4)amino, N,N-(alquilC1-4)2amino, alcanoilamino C1-4, N-(alquilC1-4)carbamoilo, N,N-(alquilC1-4) 2carbamoilo, N-(alcoxiC1-4)carbamoilo, N'-(alquilC1-4)ureido, N',N'-(alquilC1-4)2ureido, N-(alquilC1- 4)-N-(alcoxiC1-4)carbamoilo, alquilC1-4S(O)a en donde a es entre 0 y 2, alcoxicarbonilo C1-4, alcoxicarbonilamino C1-4, N-(alquilC1-4)sulfamoilo, N,N-(alquilC1-4) 2sulfamoilo, alquilsulfonilamino C1-4, alquilsulfonilaminocarbonilo C1-4, N'-(alquilC1- 4)hidrazinocarbonilo, N',N'-(alquilC1-4) 2hidrazinocarbonilo, carbociclil-R10- o heterociclil-R11-; en donde R4 y R5 en forma independiente entre sí pueden estar opcionalmente sustituidos sobre carbono por uno o más R12; y donde si dicho heterociclilo contiene una porcion -NH- dicho nitrogeno puede estar opcionalmente sustituido por un grupo seleccionado entre R13; R6 R7 y R8 se seleccionan en forma independiente entre hidrogeno o C1-4 alquilo; n es 1-4; en donde los valores de R4 pueden ser iguales o diferentes; m es 0-4; en donde los valores de R5 pueden ser iguales o diferentes; R12 se selecciona entre azido, halo, nitro, ciano, hidroxi, trifluorometoxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, alcoxi C1-4, alcanoilo C1-4, alcanoiloxi C1-4, N-(alquilC1-4)amino, N,N-(alquilC1-4)2amino, alcanoilamino C1-4, N-(alquilC1-4)carbamoilo, N,N-(alquilC1-4)2carbamoilo, alquilC1-4S(O)a, en donde a es entre 0 y 2, alcoxicarboniloC1-4, N-(alquilC1-4)sulfamoilo, N,N-(alquilC1-4)2sulfamoilo, alquilsulfonilamino C1-4, alcoxicarbonilamino C1-4, carbociclil-R14- o heterociclil-R15-; en donde R12 en forma independiente entre sí pueden estar opcionalmente sustituidos sobre carbono por uno o más R16; y en donde si dicho heterociclilo contiene una porcion -NH- dicho nitrogeno puede estar opcionalmente sustituido por un grupo seleccionado entre R17; R9, R13 y R17 se seleccionan en forma independiente entre alquilo C1-4, alcanoilo C1-4, alquilsulfonilo C1-4, alcoxicarbonilo C1-4, carbamoilo, N-(alquilC1-4)carbamoilo, N,N-(alquilC1-4)carbamoilo, bencilo, benciloxicarbonilo, benzoílo y fenilsulfonilo; R10, R11, R14 y R15 se seleccionan en forma independiente entre un enlace directo, -O-, -N(R18)-, -C(O)-, - N(R19)C(O)-, -C(O)N(R20)-, -S(O)p-, -SO2N(R21)- o -N(R22)SO2-; en donde R18, R19, R20, R21 y R22 se seleccionan en forma independiente entre hidrogeno o alquilo C1-4 y p es 0-2; R16 se selecciona entre halo, nitro, ciano, hidroxi, trifluorometoxi, trifluorometilo, amino, carboxi, carbamoilo, mercapto, sulfamoilo, metilo, etilo, etenilo, etinilo, metoxi, etoxi, acetilo, acetoxi, metilamino, etilamino, dimetilamino, dietilamino, N-metil-N- etilamino; acetilamino, N-metilcarbamoilo, N-etilcarbamoilo, N,N-dimetilcarbamoilo, N,N- dietilcarbamoilo, N-metil-N-etilcarbamoilo, metiltio, etiltio, metilsulfinilo, etilsulfinilo, mesilo, etilsulfonilo, metoxicarbonilo, etoxicarbonilo, N- metilsulfamoilo, N-etilsulfamoilo, N,N-dimetilsulfamoilo, N,N-dietilsulfalmoilo o N-metil-N-etilsulfamoilo; o una de sus sales aceptables para uso farmacéutico.
ARP060100590A 2005-02-18 2006-02-17 Derivados de piperidina con actividad antibacteriana AR053683A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US65467005P 2005-02-18 2005-02-18

Publications (1)

Publication Number Publication Date
AR053683A1 true AR053683A1 (es) 2007-05-16

Family

ID=36218455

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP060100590A AR053683A1 (es) 2005-02-18 2006-02-17 Derivados de piperidina con actividad antibacteriana

Country Status (22)

Country Link
US (2) US8399489B2 (es)
EP (1) EP1853586B1 (es)
JP (4) JP4058106B2 (es)
KR (2) KR101422432B1 (es)
CN (1) CN101163693B (es)
AR (1) AR053683A1 (es)
AU (1) AU2006215399B2 (es)
BR (1) BRPI0607756A2 (es)
CA (1) CA2598423C (es)
ES (1) ES2430569T3 (es)
HK (1) HK1114376A1 (es)
IL (1) IL185306A (es)
MX (1) MX2007010072A (es)
NO (1) NO20074703L (es)
NZ (1) NZ561613A (es)
RU (1) RU2424240C2 (es)
SA (1) SA06270020B1 (es)
TW (1) TWI402263B (es)
UA (1) UA94901C2 (es)
UY (1) UY29384A1 (es)
WO (1) WO2006087543A1 (es)
ZA (1) ZA200706920B (es)

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CN101163693B (zh) 2013-03-06
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NZ561613A (en) 2010-12-24
KR20130093174A (ko) 2013-08-21
JP2008024715A (ja) 2008-02-07
KR101422432B1 (ko) 2014-07-22
MX2007010072A (es) 2008-01-28
US8399489B2 (en) 2013-03-19
EP1853586A1 (en) 2007-11-14
UA94901C2 (ru) 2011-06-25
WO2006087543A1 (en) 2006-08-24
IL185306A0 (en) 2008-02-09
EP1853586B1 (en) 2013-07-24
RU2007134380A (ru) 2009-03-27
UY29384A1 (es) 2006-10-02
ES2430569T3 (es) 2013-11-21
BRPI0607756A2 (pt) 2010-05-18
WO2006087543A8 (en) 2007-10-18
US20100179150A1 (en) 2010-07-15
CA2598423C (en) 2014-05-27
AU2006215399A1 (en) 2006-08-24
AU2006215399B2 (en) 2010-12-09
JP2007326883A (ja) 2007-12-20
JP2008500321A (ja) 2008-01-10
HK1114376A1 (en) 2008-10-31
SA06270020B1 (ar) 2010-10-23
IL185306A (en) 2012-05-31
JP2007326882A (ja) 2007-12-20
CN101163693A (zh) 2008-04-16
JP4058106B2 (ja) 2008-03-05
KR20070113233A (ko) 2007-11-28
CA2598423A1 (en) 2006-08-24
RU2424240C2 (ru) 2011-07-20
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ZA200706920B (en) 2008-06-25
US20130150366A1 (en) 2013-06-13

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