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PE20060488A1 - Compuestos heterociclicos como inhibidores de aspartil proteasa - Google Patents

Compuestos heterociclicos como inhibidores de aspartil proteasa

Info

Publication number
PE20060488A1
PE20060488A1 PE2005000668A PE2005000668A PE20060488A1 PE 20060488 A1 PE20060488 A1 PE 20060488A1 PE 2005000668 A PE2005000668 A PE 2005000668A PE 2005000668 A PE2005000668 A PE 2005000668A PE 20060488 A1 PE20060488 A1 PE 20060488A1
Authority
PE
Peru
Prior art keywords
alkyl
aspartile
compounds
protease inhibitors
heterocyclic compounds
Prior art date
Application number
PE2005000668A
Other languages
English (en)
Inventor
Zhaoning Zhu
Brian Mckittrick
Yuanzan C Ye
Corey Strickland
William J Greenlee
Ulrich Iserloh
John Caldwell
Lingyan Wang
Michelle L Morris
Dawit Tadesse
Gang Qian
Huizhong Gu
Rachael C Hunter
Suresh D Babu
Kurt W Saionz
Thuy X H Le
Tao Guo
Andrew Stamford
Jared Cumming
Robert Mazzola
Yusheng Wu
Elizabeth M Smith
Johannes H Voigt
Zhong-Yue Sun
Original Assignee
Schering Corp
Pharmacopeia Inc
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 Schering Corp, Pharmacopeia Inc filed Critical Schering Corp
Publication of PE20060488A1 publication Critical patent/PE20060488A1/es

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    • 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
    • C07D233/66—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 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
    • C07D233/88—Nitrogen atoms, e.g. allantoin
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4168—1,3-Diazoles having a nitrogen attached in position 2, e.g. clonidine
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    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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Abstract

SE REFIERE A COMPUESTOS DE FORMULA (I), EN DONDE W ES UN ENLACE, -C(=O), -C(=S)-, -S(O)-, -N(R5)-, -C(=N(R5))-, ENTRE OTROS; X ES -N(R5)-, -O- o -C(R6)(R7)-, CON LA CONDICION DE QUE CUANDO X ES -O-, U NO SEA -O-, S(O)(1-2)-, -C(=O)- O -C(=NR5)-; U ES -S(O)(1-2)-, -C(O)-, -C(=NR5)-, -(C(R6)(R7))b-, ENTRE OTROS; CON LA CONDICION DE QUE CUANDO W ES -S(O)(1-2)-, -O-, O -N(R5)-, U NO SEA ESTOS VALORES; Y QUE CUANDO X ES -N(R5)- Y W ES -S(O)(1-2), -O- O -N(R5)-, ENTONCES U NO SEA UN ENLACE; R1, R2 Y R5 SON INDEPENSIENTEMENTE H, ALQUILO, R21-ALQUILO, ENTRE OTROS; R3 Y R4 SON INDEPENDIENTEMENTE ARILO, HETEROARILO, HETEROARIL ALQUILO, CICLOALQUILALQUILO, ENTRE OTROS. SON PREFERIDOS (6S)-(6-BROMO-PRIRIDIN-2-IL)-2-IMINO-3,6-DIMETIL-TETRAHIDROPIRIMIDIN-4(1H)-ONA, 5-CICLOPROPIL-2-IMINO-5-(3-CLORO-5-METOXI-3'-METIL-1,1'-BIFENIL)-IMIDAZOLIDIN-4-ONA, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA, QUE ADEMAS PUEDE COMPRENDER UN INHIBIDOR DE COLINESTERASA, UN INHIBIDOR DE GAMMA SECRETASA, INHIBIDOR DE HMG-CoA REDUCTASA O UN ANTIINFLAMATORIO. ESTOS COMPUESTOS SON INHIBIDORES DE LA ASPARTIL PROTEASA, POR LO QUE SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES CARDIOVASCULARES, COGNICITIVAS, NEURODEGENERATIVAS TAL COMO LA ENFERMEDAD DE ALZHEIMER
PE2005000668A 2004-12-13 2005-06-10 Compuestos heterociclicos como inhibidores de aspartil proteasa PE20060488A1 (es)

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