PE20011318A1 - SUBSTITUTE PHENYL COMPOUNDS, PHARNESILTRANSFERASE INHIBITORS - Google Patents

SUBSTITUTE PHENYL COMPOUNDS, PHARNESILTRANSFERASE INHIBITORS

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Publication number
PE20011318A1
PE20011318A1 PE2001000384A PE2001000384A PE20011318A1 PE 20011318 A1 PE20011318 A1 PE 20011318A1 PE 2001000384 A PE2001000384 A PE 2001000384A PE 2001000384 A PE2001000384 A PE 2001000384A PE 20011318 A1 PE20011318 A1 PE 20011318A1
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PE
Peru
Prior art keywords
methyl
alkylene
cycloalkyl
alkyl
inhibitors
Prior art date
Application number
PE2001000384A
Other languages
Spanish (es)
Inventor
W Hutchins Charles
T Wang Gary
M Sullivan Gerard
L Sham Hing
A Hasvold Lisa
Taka Jennings Nelson Lissa
Wang Xilu
Lin Nan-Horng
Li Qun
A Fakhoury Stephen
J O Connor Stephen
L Gwaltney Ii Stephen
Wang Wei-Bo
L Curtin Michael
Original Assignee
Abbott Lab
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Application filed by Abbott Lab filed Critical Abbott Lab
Publication of PE20011318A1 publication Critical patent/PE20011318A1/en

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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30Oxygen atoms
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    • A61P17/06Antipsoriatics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
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    • 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
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • 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
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    • C07D233/64Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
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    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
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    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
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  • Chemical & Material Sciences (AREA)
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  • Ophthalmology & Optometry (AREA)
  • Dermatology (AREA)
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  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

SE REFIERE A COMPUESTOS FENILO SUSTITUIDOS DE FORMULA I DONDE A1 ES L1-M1-L2, ALQUILENO, DONDE EL ALQUILENO PUEDE ESTAR SUSTITUIDOS CON OH, OXO, Q1-Q2-R3, CON LA CONDICION QUE CUANDO A1 ES METILENO, EL METILENO ESTA SUSTITUIDO; L1 Y L2 SON ALQUILENO CON ALQUILO, CICLOALQUILO, CICLOALQUILALQUILO, ENTRE OTROS; M1 ES O, N(R4), N(R5)SO2, SO2N(R5), N(R5)C(O), ENTRE OTROS; Q1 ES O, N(R4), N(R5)C(O), N(R5)SO2, ENTRE OTROS; Q2 ES ALQUILENO, ALQUENILENO, ALQUINILENO; R1 ES HALO, CICLOALQUILO, ARILO, HETEROARILO; R2 ES HETEROARILO TAL COMO IMIDAZOLILO, PIRAZOLILO, PIRROLILO, ENTRE OTROS; R3 ES ALQUILO, CICLOALQUILO, ARILO, ENTRE OTROS; R4 ES H, ALQUILO, ALQUENILO, ALQUINILO, ALCANOILO, ENTRE OTROS; R5 ES H, ALQUILO, ARILO, ARILALQUILO, CICLOALQUILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS CLORHIDRATO DE 5-(BENCILOXI)(6-FLUORO-2'METIL(1,1'-BIFENIL)-3-IL)METIL)-1-METIL-1H-IMIDAZOL,CLORHIDRATO DE 2'-METIL(1,1'-BIFENIL)-3-IL)(-1-METIL-1H-IMIDAZOL-5-IL)METILETER BENCILICO,CLORHIDRATO DE 5-(BENCILOXI)(6-CLORO-2'METIL(1,1'-BIFENIL)-3-IL)METIL)-1-METIL-1H-IMIDAZOL, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO PARA LA PREPARACION Y A COMPOSICIONES FARMACEUTICAS. LOS COMPUESTOS FENILO SUSTITUIDOS SON INHIBIDORES DE LA FARNESIL TRANSFERASA UTILES PARA EL TRATAMIENTO DE CANCERREFERS TO SUBSTITUTED PHENYL COMPOUNDS OF FORMULA I WHERE A1 IS L1-M1-L2, ALKYLENE, WHERE THE ALKYLENE MAY BE SUBSTITUTED WITH OH, OXO, Q1-Q2-R3, WITH THE CONDITION THAT WHEN A1 IS METHYLENE, METHYLENE IS SUBSTITUTED ; L1 AND L2 ARE ALKYLENE WITH ALKYL, CYCLOALKYL, CYCLOALKYLALKYL, AMONG OTHERS; M1 IS O, N (R4), N (R5) SO2, SO2N (R5), N (R5) C (O), AMONG OTHERS; Q1 IS O, N (R4), N (R5) C (O), N (R5) SO2, AMONG OTHERS; Q2 IS ALKYLENE, ALKENYLENE, ALKYLENE; R1 IS HALO, CYCLOALKYL, ARYL, HETEROARYL; R2 IS HETEROARYL SUCH AS IMIDAZOLIL, PYRAZOLIL, PYRROLYL, AMONG OTHERS; R3 IS ALKYL, CYCLOALKYL, ARYL, AMONG OTHERS; R4 IS H, ALKYL, ALKENYL, ALKINYL, ALCANOYL, AMONG OTHERS; R5 IS H, ALKYL, ARYL, ARYLALKYL, CYCLOALKYL, AMONG OTHERS. PREFERRED COMPOUNDS 5- (BENZYLOXY) (6-FLUORO-2'-METHYL (1,1'-BIPHENYL) -3-IL) METHYL) -1-METHYL-1H-IMIDAZOLE HYDROCHLORIDE, 2'-METHYL HYDROCHLORIDE (1 , 1'-BIPHENYL) -3-IL) (- 1-METHYL-1H-IMIDAZOL-5-IL) BENZYL METHYLETER, 5- (BENZYLOXY) (6-CHLORO-2'-METHYL (1,1'-BIPHENYL) HYDROCHLORIDE ) -3-IL) METHYL) -1-METHYL-1H-IMIDAZOLE, AMONG OTHERS. IT ALSO REFERS TO A PROCEDURE FOR THE PREPARATION AND TO PHARMACEUTICAL COMPOSITIONS. THE SUBSTITUTED PHENYL COMPOUNDS ARE INHIBITORS OF FARNESIL TRANSFERASE USEFUL FOR THE TREATMENT OF CANCER

PE2001000384A 2000-04-27 2001-04-27 SUBSTITUTE PHENYL COMPOUNDS, PHARNESILTRANSFERASE INHIBITORS PE20011318A1 (en)

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US82220501A 2001-04-02 2001-04-02

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JP (1) JP2004509064A (en)
AU (1) AU2001259218A1 (en)
CA (1) CA2407093A1 (en)
HK (1) HK1053833A1 (en)
MX (1) MXPA02010608A (en)
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WO (1) WO2001081316A2 (en)

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