BRPI9811679B8 - antifúngicos de 1-{4-[4-(4-{[4-fenil-4-(1 h-1,2,4-triazol-1-ilmetil)-1,3-dioxolan-2-il]metóxi}fenil)piperazin-1-il]fenil}imidazolidin-2-onas substituídas - Google Patents

antifúngicos de 1-{4-[4-(4-{[4-fenil-4-(1 h-1,2,4-triazol-1-ilmetil)-1,3-dioxolan-2-il]metóxi}fenil)piperazin-1-il]fenil}imidazolidin-2-onas substituídas

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Publication number
BRPI9811679B8
BRPI9811679B8 BRPI9811679A BR9811679A BRPI9811679B8 BR PI9811679 B8 BRPI9811679 B8 BR PI9811679B8 BR PI9811679 A BRPI9811679 A BR PI9811679A BR 9811679 A BR9811679 A BR 9811679A BR PI9811679 B8 BRPI9811679 B8 BR PI9811679B8
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BR
Brazil
Prior art keywords
phenyl
antifungals
aryl
alkyl
hydrogen
Prior art date
Application number
BRPI9811679A
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English (en)
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BR9811679A (pt
BRPI9811679B1 (pt
Inventor
Christopher Odds Frank
Florent Adolf Vanden Bossche Hugo
Heeres Jan
Meerpoel Lieven
Jozef Elisabeth Van Der Veken Louis
Original Assignee
Janssen Pharmaceutica Nv
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.)
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Publication date
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of BR9811679A publication Critical patent/BR9811679A/pt
Publication of BRPI9811679B1 publication Critical patent/BRPI9811679B1/pt
Publication of BRPI9811679B8 publication Critical patent/BRPI9811679B8/pt

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic 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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pyrrole Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

patente de invenção: <b>"antifúngicos de 1,3-dioxolanos 2,4,4-trissubstituídos"<d>. a invenção refere-se a novos compostos de fórmula (i), a uma forma n-óxido, a um sal de adição de ácido farmaceuticamente aceitável ou a uma forma estereoquimicamente isomérica dos compostos, nos quais n é zero, 1, 2 ou 3; x é n ou ch; cada r¹ independentemente é halo, nitro, ciano, amino, hidroxi, c~ 1-4~ alquila, c~ 1-4~ alquiloxi ou trifluormetila; r² é hidrogênio; c~ 3-7~ alquenila; c~ 3-7~ alquinila, arila; c~ 3-7~ cicloalquila; opcionalmente c~ 1-6~ alquila substituída; r³ e r^ 4^ cada um independentemente são hidrogênio, c~ 1-6~ alquila, c~ 3-7~ cicloalquila ou arila; ou r³ e r^ 4^ tomados juntamente formam um radical bivalente -r³ -r^ 4^- de fórmula (a), (b), (c), (d) ou (e), onde r^ 5a^, r^ 5b^, r^ 5c^ e r^ 5d^, cada um independentemente, são hidrogênio, c~ 1-6~ alquila ou arila; e arila é fenila opcionalmente substituída; como antifúngicos; sua preparação, composições que contêm os compostos e seu uso como medicamento.
BRPI9811679A 1997-07-11 1998-07-07 antifúngicos de 1-{4-[4-(4-{[4-fenil-4-(1 h-1,2,4-triazol-1-ilmetil)-1,3-dioxolan-2-il]metóxi}fenil)piperazin-1-il]fenil}imidazolidin-2-onas substituídas BRPI9811679B8 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP97202181 1997-07-11
PCT/EP1998/004194 WO1999002523A1 (en) 1997-07-11 1998-07-07 2,4,4-trisubstituted-1,3-dioxolane antifungals

Publications (3)

Publication Number Publication Date
BR9811679A BR9811679A (pt) 2000-09-19
BRPI9811679B1 BRPI9811679B1 (pt) 2016-10-18
BRPI9811679B8 true BRPI9811679B8 (pt) 2021-05-25

Family

ID=8228553

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI9811679A BRPI9811679B8 (pt) 1997-07-11 1998-07-07 antifúngicos de 1-{4-[4-(4-{[4-fenil-4-(1 h-1,2,4-triazol-1-ilmetil)-1,3-dioxolan-2-il]metóxi}fenil)piperazin-1-il]fenil}imidazolidin-2-onas substituídas

Country Status (34)

Country Link
US (1) US6387906B1 (pt)
EP (1) EP1068200B1 (pt)
KR (1) KR100540460B1 (pt)
AP (1) AP1379A (pt)
AR (1) AR015130A1 (pt)
AT (1) ATE289303T1 (pt)
AU (1) AU749760B2 (pt)
BG (1) BG64314B1 (pt)
BR (1) BRPI9811679B8 (pt)
CA (1) CA2295090C (pt)
CZ (1) CZ297453B6 (pt)
DE (1) DE69829082T2 (pt)
DK (1) DK1068200T3 (pt)
EA (1) EA002828B1 (pt)
EE (1) EE04155B1 (pt)
ES (1) ES2238765T3 (pt)
GE (1) GEP20033054B (pt)
HK (1) HK1032404A1 (pt)
HR (1) HRP20000007B1 (pt)
HU (1) HU225159B1 (pt)
ID (1) ID23783A (pt)
IL (1) IL133919A (pt)
MY (1) MY118844A (pt)
NO (1) NO318328B1 (pt)
NZ (1) NZ501982A (pt)
PL (1) PL193703B1 (pt)
PT (1) PT1068200E (pt)
SI (1) SI1068200T1 (pt)
SK (1) SK285321B6 (pt)
TR (1) TR200000154T2 (pt)
TW (1) TW593312B (pt)
UA (1) UA71543C2 (pt)
WO (1) WO1999002523A1 (pt)
ZA (1) ZA986160B (pt)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19945982A1 (de) * 1999-09-24 2001-03-29 Knoll Ag Geschwindigkeitsbestimmte Partikel
US20040086567A1 (en) * 2002-10-30 2004-05-06 Pawan Seth Bioequivalent composition of itraconazole and a hydrophilic polymer
AU2009223833A1 (en) * 2008-03-03 2009-09-17 Stiefel Laboratories, Inc. Processes for preparing enantiomerically pure diol and dioxolane compounds
US8431699B2 (en) * 2009-02-27 2013-04-30 Vertichem Corporation Method for manufacture of 2-oxoimidazolidines
CN105777486B (zh) * 2016-03-30 2018-09-11 浙江大学宁波理工学院 一种2-[2-(2,4-二氟苯基)-2-丙烯-1-基]-1,3-丙二醇的合成方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4218458A (en) * 1978-06-23 1980-08-19 Janssen Pharmaceutica, N.V. Heterocyclic derivatives of (4-aryloxy-methyl-1,3-dioxolan-2-yl)methyl-1H-imidazoles and 1H-1,2,4-triazoles
US4619931A (en) * 1983-02-28 1986-10-28 Janssen Pharmaceutica, N.V. [[4-[4-(4-phenyl-1-piperazinyl)phenoxymethyl]-1,3-dioxolan-2-yl]methyl]-1H-imidazoles and 1H-1,2,4-triazoles
CA1292472C (en) 1985-12-03 1991-11-26 Alfonsus Guilielmus Knaeps Derivatives of ¬¬4-¬4-(4-phenyl-1-piperazinyl)- phenoxymethyl|-1,3-dioxolan-2-yl|methyl|-1h-imidazoles and 1h-1,2,4-triazoles
US4788190A (en) 1986-12-24 1988-11-29 Schering Corporation 2,4,4-tri- and 2,2,4,4-tetra substituted-1,3-dioxolane antifungal, antiallergy compounds
NZ233502A (en) * 1989-06-09 1991-11-26 Janssen Pharmaceutica Nv 4-(1,2,4-triazole- or imidazole-phenyl-substituted) -1-(1,3-dioxolan-4-ylmethoxyphenyl) piperazine derivatives; preparatory processes: fungicidal and antiviral compositions
IL103558A0 (en) 1991-10-30 1993-03-15 Schering Corp Tri-substituted tetrahydrofuran antifungals
PL181947B1 (en) * 1994-01-24 2001-10-31 Janssen Pharmaceutica Nv Water-soluble azole-type antimycotic agents

Also Published As

Publication number Publication date
ID23783A (id) 2000-05-11
SI1068200T1 (pt) 2005-08-31
GEP20033054B (en) 2003-08-25
IL133919A0 (en) 2001-04-30
TR200000154T2 (tr) 2000-06-21
EA200000116A1 (ru) 2000-08-28
MY118844A (en) 2005-01-31
CA2295090C (en) 2009-09-08
HRP20000007B1 (en) 2008-12-31
CA2295090A1 (en) 1999-01-21
HUP0004459A2 (hu) 2002-04-29
DK1068200T3 (da) 2005-06-20
ES2238765T3 (es) 2005-09-01
WO1999002523A1 (en) 1999-01-21
TW593312B (en) 2004-06-21
AR015130A1 (es) 2001-04-18
HUP0004459A3 (en) 2002-11-28
AP1379A (en) 2005-03-29
PL193703B1 (pl) 2007-03-30
EE200000020A (et) 2000-10-16
AU8857698A (en) 1999-02-08
NO318328B1 (no) 2005-03-07
CZ463799A3 (cs) 2000-04-12
EA002828B1 (ru) 2002-10-31
NO20000114L (no) 2000-03-13
US6387906B1 (en) 2002-05-14
IL133919A (en) 2002-02-10
UA71543C2 (uk) 2004-12-15
CZ297453B6 (cs) 2006-12-13
EP1068200B1 (en) 2005-02-16
ATE289303T1 (de) 2005-03-15
PT1068200E (pt) 2005-07-29
SK285321B6 (sk) 2006-11-03
NZ501982A (en) 2000-10-27
KR100540460B1 (ko) 2006-01-12
NO20000114D0 (no) 2000-01-10
BG103982A (en) 2000-08-31
BR9811679A (pt) 2000-09-19
PL338009A1 (en) 2000-09-25
BRPI9811679B1 (pt) 2016-10-18
HK1032404A1 (en) 2001-07-20
DE69829082D1 (de) 2005-03-24
EP1068200A1 (en) 2001-01-17
HU225159B1 (en) 2006-07-28
HRP20000007A2 (en) 2000-12-31
SK184199A3 (en) 2000-07-11
BG64314B1 (bg) 2004-09-30
AP2000001730A0 (en) 2000-03-31
EE04155B1 (et) 2003-10-15
DE69829082T2 (de) 2005-12-29
AU749760B2 (en) 2002-07-04
KR20010020576A (ko) 2001-03-15
ZA986160B (en) 2000-01-10

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