CO5080801A1 - Inhibidores de proteasas - Google Patents

Inhibidores de proteasas

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Publication number
CO5080801A1
CO5080801A1 CO99030929A CO99030929A CO5080801A1 CO 5080801 A1 CO5080801 A1 CO 5080801A1 CO 99030929 A CO99030929 A CO 99030929A CO 99030929 A CO99030929 A CO 99030929A CO 5080801 A1 CO5080801 A1 CO 5080801A1
Authority
CO
Colombia
Prior art keywords
alkyl
phenyl
substituted
group
thiophene
Prior art date
Application number
CO99030929A
Other languages
English (en)
Inventor
William Edward Bondinell
Dennis Shinji Yamashita
Renee Louise Desjarlais
Daniel Frank Veber
Original Assignee
Smithkline Beecham Corp
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Filing date
Publication date
Application filed by Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of CO5080801A1 publication Critical patent/CO5080801A1/es

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    • C07D213/00Heterocyclic 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
    • 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
    • C07D213/89Heterocyclic 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 with hetero atoms directly attached to the ring nitrogen atom
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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    • A61P3/14Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
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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
    • C07D213/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/14Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/155Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
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    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/82Benzo [b] furans; Hydrogenated benzo [b] furans with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
    • C07D307/84Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
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    • C07K5/06Dipeptides
    • C07K5/06008Dipeptides with the first amino acid being neutral
    • C07K5/06017Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06026Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
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    • C07K5/06Dipeptides
    • C07K5/06139Dipeptides with the first amino acid being heterocyclic
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  • Animal Behavior & Ethology (AREA)
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  • Proteomics, Peptides & Aminoacids (AREA)
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  • Obesity (AREA)
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  • Diabetes (AREA)
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  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Furan Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
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Abstract

Un compuesto de fórmula I:<EMI FILE="99030929_1" ID="1" IMF=JPEG >R1 y R2 son independientemente H o alquilo C1-C6, siempre y cuando R1 y R2 no sean ambos alquilo C1-C6;P es<EMI FILE="99030929_2" ID="2" IMF=JPEG >R3 se elige entre el grupo formado por CH2CH(CH3)2, CH2CH2CH3, CH2CH=CH2 ó CH2Ph;R4 se elige entre el grupo formado por:alquilo C0-C6;N-piperizina;N-tetrahidroisoquinoleína;alquilo C0-C6; sustituido con fenilo, tiofeno, benzotiazol, 2-, 3-, 4-, 5-, 6- ó 7-quinoleína, naftilo, 1-(7-nitro-2,1,3-benzoxadiazol-4-il)-L-prolilo, alquil (C0-C6)pirazol, N-Cbz-2-(N,N-dimetilamino)etilglicil-, N-metilpirrol, benzoxazol, benciloxi, alcoxi C1-C6; 2, 3, ó 4-piridiniloxi; adamantilo, tieno[3, 2-b]tiofeno;fenilo; tiofeno; benzotiofeno; benzofurano, benzotiazol; 2-, 3-, 4-, 5-, 6- ó 7-quinoleína; naftilo y benzoxazol, cada uno de ellos independientemente sustituido con uno o más de los grupos alquilo C1-C6, halógeno nitro, ciano, hidroxi, alcoxi C1-C6, trifluorometilo, carboxilo, éster carboxi-alquilo (C1-C6), alquil (C0-C6 )2 N-alquilo C0 -C6, alquil (C0-C6 )2 N-alcoxi C0-C6, N-(C0-C6 )-N-piperizina, N-(N-alquil(C0-C6)-N-piperidina)-4-alquil(C0-C6)-amina, (alquil(C0-C6)2 N-alquil (C0-C6)-alquil (C0-C6)-amina, N-morfolino-alquilo C0-C6, N-morfolino-alcoxi C0-C6, fenilo, tiofeno, benzotiazol, 2, 3, 4, 5, 6, ó 7-quinoleína, naftilo, alquil (C0-C6)pirazol, N-metil-pirrol, benzoxazol;benciloxi sustituido con uno o más grupos alquilo (C1-C6), halógeno, nitro, ciano, hidroxi, alcoxi (C1-C6 ), trifluorometilo, carboxilo, éster carboxi alquilo (C1-C6), fenilo, tiofeno, benzotiazol, 2, 3, 4, 5, 6, ó 7 quinoleína, naftilo, alquil (C0 -C6 )pirazol, N-metil-pirrol, y benzoxazol; y pirazina;pirimidina;2,7-dimetilpirazolo [1, 5a ]pirimidina y - 2 -4,7-dimetilpirazolo [5,1-c][1,2,4]-triazina.R6 se elige entre el grupo formado por fenilo y fenilo sustituido con alquilo (C0-C6), N-piperidina, benzofurano; o 2, 3 ó 4 piridina;Q es<EMI FILE="99030929_3" ID="3" IMF=JPEG >En la que:R7 se elige entre el grupo formado por fenilo y fenilo sustituido con alquilo C0-C6), N-piperidina, benzofurano; o 2, 3 ó 4 piridina;R8 se elige entre el grupo formado por H, CH2CH(CH3)2, CH2CH2CH3 y CH2CH=CH2, CH2 Ph, cuando R9 es H; oR8 y R9 se eligen independientemente entre el grupo formado por alquilo (C1-C6); 3-(2-piridil)-fenilacetilo; 3-bifenil-acetilo; 3-(2-piridil)-fenilacetilo sustituido con 2-alquilo (C1-C6); 3-bifenil-acetilo sustituido con 2-alquilo (C1-C6); 3-(2-piridil)-fenilacetilo disustituido con 2,2-alquilo (C1-C6); 3-bifenil-acetilo disustituido con 2,2-alquilo (C1-C6), (C1-C6), fenil-sulfonilo; 2-, 3- ó 4-pirina-sulfonilo; fenilo; alquil (C0-C6)sulfonilo; alquil (C0-C6) carbonilo; yfenil-sulfonilo; fenilo; alquil (C0-C6) sulfonilo; o alquil(C0-C6)carbonilo sustituidos independientemente con uno o más grupos alquilo (C1-C6), halógeno, nitro, ciano, hidroxi, alcoxi (C1-C6), trifluorometilo, carboxilo, éster carboxialquilo (C1-C6 ), fenilo , tiofeno, benzotiazol, 2-, 3-, 4-, 5-, 6- ó 7-quinoleína, naftilo, alquil(C0-C6) pirazol, N-metil-pirrol, benzoxazol;y sus sales, hidratos y solvatos aceptables farmacéuticamente.Compuestos según la reivindicación 1 administrables a pacientes para inhibir proteasas del grupo formado por proteasa de cicteína y de serina.1Compuestos conforme a la reivindicación o punto 1 administrables en pacientes afectados por degradación excesiva de cartílago o de matriz.2Compuestos según la reivindicaciones 3 y 23 administrables contra la osteoporosis.2Compuestos según la reivindicación 3 y 23 administrables contra la artritis rumatoide.
CO99030929A 1998-05-21 1999-05-20 Inhibidores de proteasas CO5080801A1 (es)

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US (1) US6518267B1 (es)
EP (1) EP1067894A4 (es)
JP (1) JP2002515411A (es)
AR (1) AR018370A1 (es)
AU (1) AU4092799A (es)
CA (1) CA2332531A1 (es)
CO (1) CO5080801A1 (es)
DZ (1) DZ2796A1 (es)
MA (1) MA26631A1 (es)
WO (1) WO1999059526A2 (es)

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US6586466B2 (en) 1995-10-30 2003-07-01 Smithkline Beecham Corporation Carbohydrazide-protease inhibitors
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US20030144175A1 (en) 1998-12-23 2003-07-31 Smithkline Beecham Corporation Protease inhibitors
US6596715B1 (en) 1999-11-10 2003-07-22 Smithkline Beecham Corporation Protease inhibitors
AU1474801A (en) 1999-11-10 2001-06-06 Smithkline Beecham Corporation Protease inhibitors
US6583137B1 (en) 1999-11-10 2003-06-24 Smithkline Beecham Corporation Protease inhibitors
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KR20040097375A (ko) * 2002-04-23 2004-11-17 시오노기 앤드 컴파니, 리미티드 피라졸로[1, 5-에이]피리미딘 유도체 및 이를 함유한엔에이디(피)에이취 산화효소 저해제
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UY29101A1 (es) * 2004-09-07 2006-03-31 Smithkline Beecham Corp 1,3-diaminas aceclicas y usos de las mismas
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CN104311408B (zh) * 2014-09-12 2019-11-08 沈阳化工研究院有限公司 4,4’-二苯醚二甲酸的制备方法
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MA26618A1 (fr) * 1998-04-09 2004-12-20 Smithkline Beecham Corp Composes et compositions pharmaceutiques pour le traitement du paludisme

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DZ2796A1 (fr) 2003-12-01
MA26631A1 (fr) 2004-12-20
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