FI865257A - Derivat av nya //4-/4-(4-fenyl -piperazinyl) fenoximetyl/-1,3-dioxolan-2-yl/metyl-1h-imidazoler och 1h-1,2,4-triazoler. - Google Patents

Derivat av nya //4-/4-(4-fenyl -piperazinyl) fenoximetyl/-1,3-dioxolan-2-yl/metyl-1h-imidazoler och 1h-1,2,4-triazoler. Download PDF

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Publication number
FI865257A
FI865257A FI865257A FI865257A FI865257A FI 865257 A FI865257 A FI 865257A FI 865257 A FI865257 A FI 865257A FI 865257 A FI865257 A FI 865257A FI 865257 A FI865257 A FI 865257A
Authority
FI
Finland
Prior art keywords
triazoler
phenoximethyl
imidazoler
dioxolan
piperazinyl
Prior art date
Application number
FI865257A
Other languages
English (en)
Other versions
FI88505B (fi
FI865257A0 (fi
FI88505C (fi
Inventor
Jan Heeres
Leo J J Backx
Jozef Bertha August Thijssen
Alfonsus Guilielmus Knaeps
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.)
Filing date
Publication date
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of FI865257A0 publication Critical patent/FI865257A0/fi
Publication of FI865257A publication Critical patent/FI865257A/fi
Publication of FI88505B publication Critical patent/FI88505B/fi
Application granted granted Critical
Publication of FI88505C publication Critical patent/FI88505C/fi

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic 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
    • C07D231/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic 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
    • C07D233/56—Heterocyclic 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)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
FI865257A 1985-12-23 1986-12-22 Foerfarande foer framstaellning av nya, terapeutiskt anvaendbara //4-/4-(4-fenyl-1-piperazinyl)fenoximetyl/-1,3-dioxolan-2-yl/metyl-1H-imidazol- och -1H-1,2,4-triazolderivat FI88505C (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US81267085A 1985-12-23 1985-12-23
US81267085 1985-12-23

Publications (4)

Publication Number Publication Date
FI865257A0 FI865257A0 (fi) 1986-12-22
FI865257A true FI865257A (fi) 1987-06-24
FI88505B FI88505B (fi) 1993-02-15
FI88505C FI88505C (fi) 1993-05-25

Family

ID=25210297

Family Applications (1)

Application Number Title Priority Date Filing Date
FI865257A FI88505C (fi) 1985-12-23 1986-12-22 Foerfarande foer framstaellning av nya, terapeutiskt anvaendbara //4-/4-(4-fenyl-1-piperazinyl)fenoximetyl/-1,3-dioxolan-2-yl/metyl-1H-imidazol- och -1H-1,2,4-triazolderivat

Country Status (18)

Country Link
EP (1) EP0228125B1 (fi)
JP (2) JPH0749428B2 (fi)
AT (1) ATE73799T1 (fi)
AU (2) AU589726B2 (fi)
CA (1) CA1292472C (fi)
CY (1) CY1825A (fi)
DE (1) DE3684431D1 (fi)
DK (2) DK164167C (fi)
ES (1) ES2032381T3 (fi)
FI (1) FI88505C (fi)
GR (1) GR3004114T3 (fi)
HK (1) HK46295A (fi)
IE (1) IE59564B1 (fi)
IL (1) IL81054A (fi)
NO (1) NO167917C (fi)
NZ (1) NZ218553A (fi)
PT (1) PT84007B (fi)
ZA (1) ZA869637B (fi)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ223799A (en) * 1987-03-25 1989-12-21 Janssen Pharmaceutica Nv Azolylmethyl-dioxolanylmethoxyphenyl-piperazinyl-phenyl-triazolones and antimicrobial compositions
CA1331757C (en) 1988-02-29 1994-08-30 Janssen Pharmaceutica Naamloze Vennootschap 5-lipoxygenase inhibiting 4-(4-phenyl-1-piperazinyl)phenols
GR1000302B (el) * 1988-07-01 1992-05-12 Janssen Pharmaceutica Nv Μεθοδος παρασκευης παραγωγων 2,4-διυδρο-3η-1,2,4-τριαζολ-3-ονης.
GR1000298B (el) * 1988-07-01 1992-05-12 Janssen Pharmaceutica Nv Μεθοδος παρασκευης παραγωγων 2,4-διυδρο-3η-1,2,4-τριαζολ-3-ονης.
GR1000330B (el) * 1988-07-01 1992-06-25 Janssen Pharmaceutica Nv Μεθοδος παρασκευης παραγωγων 2,4 διυδρο-3η-1,2,4-τριαζολ-3-ονης.
GR1000297B (el) * 1988-07-01 1992-05-12 Janssen Pharmaceutica Nv Μεθοδος παρασκευης παραγωγων 2,4-διυδρο-3η-1,2,4-τριαζολ-3-ονης.
GB8903592D0 (en) * 1989-02-16 1989-04-05 Boots Co Plc Therapeutic agents
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
CA2076257A1 (en) * 1991-09-13 1993-03-14 Jan Heeres 4-¬4-¬4-(4-hydroxyphenyl)-1- piperazinyl|phenyl|-5-methyl-3h -1,2,4-triazol-3-one derivatives
TW279864B (fi) * 1993-02-19 1996-07-01 Janssen Pharmaceutica Nv
CO4520281A1 (es) * 1993-12-21 1997-10-15 Schering Corp Antifungicos de tetrahidrofurano
KR100352147B1 (ko) * 1994-01-24 2002-11-11 얀센 파마슈티카 엔.브이. 수용성아졸항진균제
US5571811A (en) * 1994-07-12 1996-11-05 Janssen Pharmaceutica N.V. Sulfonamide derivatives of azolones
CN1068000C (zh) * 1994-10-27 2001-07-04 詹森药业有限公司 阿朴脂蛋白－b合成抑制剂
US5625064A (en) * 1995-04-19 1997-04-29 Schering Corporation Process for the preparation of triazolones
TW457240B (en) * 1995-04-20 2001-10-01 Janssen Pharmaceutica Nv Novel triazolones as apolipoprotein-B synthesis inhibitors
WO1997000248A1 (en) * 1995-06-19 1997-01-03 Schering Corporation Hydroxyalkyl-substituted triazolones antifungals
JP2001504121A (ja) * 1996-11-12 2001-03-27 セプラコール，インク． ２ｒ，４ｓ，ｒ，ｓ―および２ｓ，４ｒ，ｒ，ｓ―ヒドロキシイトラコナゾール―およびヒドロキシサパーコナゾール誘導体
AU773405B2 (en) * 1996-11-12 2004-05-27 Sepracor, Inc. Hydroxyitraconazole enantiomer mixtures
JP4473350B2 (ja) * 1997-07-11 2010-06-02 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ ２，４，４−三置換−１，３−ジオキソラン抗菌・抗カビ剤
TW593312B (en) * 1997-07-11 2004-06-21 Janssen Pharmaceutica Nv 2,4,4-trisubstituted-1,3-dioxolane antifungals
WO1999018111A1 (en) * 1997-10-07 1999-04-15 Schering Corporation Crystalline antifungal glycine ester polymorph
BR0010279A (pt) 1999-05-04 2002-05-14 Janssen Phamaceutica N V éteres antifúngicos
KR100342383B1 (ko) * 1999-06-17 2002-12-06 한국화학연구원 이소옥사졸리딘 유도체, 그의 제조 방법 및 그를 포함하는 살균제 조성물
US9040539B2 (en) * 2010-05-19 2015-05-26 Sandoz Ag Process for the preparation of chiral triazolones
JP6669751B2 (ja) 2014-12-05 2020-03-18 プルモシデ リミテド 抗真菌化合物
JP6811727B2 (ja) 2015-05-21 2021-01-20 プルモシデ リミテド 抗真菌性の４−（４−（４−（（（３ｒ，５ｒ）−５−（（１ｈ−１，２，４−トリアゾール−１−イル）メチル）−５−（２，４−ジフルオロフェニル）テトラヒドロフラン−３−イル）メトキシ）−３−メチルフェニル）ピペラジン−１−イル）−ｎ−（２−ヒドロキシシクロヘキシル）ベンズアミド、又はその医薬として許容し得る塩

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4144346A (en) * 1977-01-31 1979-03-13 Janssen Pharmaceutica N.V. Novel 1-(1,3-dioxolan-2-ylmethyl)-1H-imidazoles
US4267179A (en) * 1978-06-23 1981-05-12 Janssen Pharmaceutica, N.V. Heterocyclic derivatives of (4-phenylpiperazin-1-yl-aryloxymethyl-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

Also Published As

Publication number Publication date
DK74691D0 (da) 1991-04-23
CY1825A (en) 1995-12-01
DK164167B (da) 1992-05-18
NO167917C (no) 1991-12-27
FI88505B (fi) 1993-02-15
AU589726B2 (en) 1989-10-19
FI865257A0 (fi) 1986-12-22
FI88505C (fi) 1993-05-25
ES2032381T3 (es) 1993-02-16
DK74691A (da) 1991-04-23
NZ218553A (en) 1990-06-26
DK625586A (da) 1987-06-24
AU1607688A (en) 1988-08-04
DK164167C (da) 1992-10-12
HK46295A (en) 1995-04-07
EP0228125A1 (en) 1987-07-08
AU6685386A (en) 1987-06-25
GR3004114T3 (fi) 1993-03-31
DE3684431D1 (de) 1992-04-23
CA1292472C (en) 1991-11-26
ZA869637B (en) 1988-08-31
NO167917B (no) 1991-09-16
DK625586D0 (da) 1986-12-22
NO865235L (no) 1987-06-24
AU593736B2 (en) 1990-02-15
PT84007B (pt) 1989-06-30
PT84007A (en) 1987-01-01
JPH07285963A (ja) 1995-10-31
EP0228125B1 (en) 1992-03-18
IL81054A (en) 1992-03-29
NO865235D0 (no) 1986-12-22
IE59564B1 (en) 1994-03-09
IE863369L (en) 1987-06-23
ATE73799T1 (de) 1992-04-15
DK167356B1 (da) 1993-10-18
JPH0749428B2 (ja) 1995-05-31
IL81054A0 (en) 1987-03-31
JP2574656B2 (ja) 1997-01-22
JPS62158275A (ja) 1987-07-14

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FG Patent granted

Owner name: JANSSEN PHARMACEUTICA N.V.

BB Publication of examined application
MM Patent lapsed

Owner name: JANSSEN PHARMACEUTICA N.V.