PE20070017A1 - Derivados n-amida de 8-azabiciclo[3.2.1]oct-3-ilo como antagonistas de ccr1 - Google Patents

Derivados n-amida de 8-azabiciclo[3.2.1]oct-3-ilo como antagonistas de ccr1

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Publication number
PE20070017A1
PE20070017A1 PE2006000656A PE2006000656A PE20070017A1 PE 20070017 A1 PE20070017 A1 PE 20070017A1 PE 2006000656 A PE2006000656 A PE 2006000656A PE 2006000656 A PE2006000656 A PE 2006000656A PE 20070017 A1 PE20070017 A1 PE 20070017A1
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PE
Peru
Prior art keywords
alkyl
halogen
alcoxy
octan
azabicyclo
Prior art date
Application number
PE2006000656A
Other languages
English (en)
Inventor
Forner Maria Dolors Fernandez
Toribio Maria Estrella Lozoya
Belart Emma Terricabras
Original Assignee
Almirall Prodesfarma Sa
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 Almirall Prodesfarma Sa filed Critical Almirall Prodesfarma Sa
Publication of PE20070017A1 publication Critical patent/PE20070017A1/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D451/00Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/439Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
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Abstract

SE REFIERE A COMPUESTOS N-AMIDA DE 8-AZABICICLO[3.2.1]OCT-3-ILO DE FORMULA (I) DONDE n ES DE 1 A 4; m ES DE 1 A 3; p ES DE 0 A 2; R1, R2 Y R3 SON H O ALQUILO(C1-C4); Q ES UN ENLACE DIRECTO, CONR9, OCONR9, NR9, ENTRE OTROS, DONDE R9 ES H O ALQUILO(C1-C4); R4 ES H, ALQUILO(C1-C4) OPCIONALMENTE SUSTITUIDO CON COOH, FENILO O SCH3; R5 Y R6 SON H, ALQUILO(C1-C4), FENILO O R5 Y R6 JUNTO CON EL ATOMO DE CARBONO AL QUE ESTAN UNIDOS FORMAN UN CICLOALQUILO(C3-C8); R7 Y R8 SON H, HALOGENO O ALCOXI(C1-C4); A ES UN COMPUESTO DE FORMULA (i) O (ii), DONDE D ES UN ENLACE DIRECTO, O U CH2CH2; R11 ES H, HALOGENO, ALCOXI(C1-C4), NITRO, ENTRE OTROS; R12 ES CIANO, ALQUILO(C1-C4), ALCOXI(C1-C4), HALOGENO O CF3; q ES DE 0 A 2; R13 ES H O ALQUILO(C1-C4); R14 ES H O HALOGENO. SON COMPUESTOS PREFERIDOS: 5-CLORO-2-(3-((3-ENDO)-8-(4-CLOROBENCIL)-8-AZABICICLO[3.2.1]OCTAN-3-ILAMINO)-3-OXOPROPOXI)-N-METILBENZAMIDA, 3-(4-CLORO-2-UREIDOFENOXI)-N-((3-ENDO)-8-(4-CLOROBENCIL)-8-AZABICICLO[3.2.1]OCTAN-3-IL)PROPANAMIDA, 5-CLORO-2-(4-((3-ENDO)-8-(4-CLOROBENCIL)-8-AZABICICLO[3.2.1]OCTAN-3-ILAMINO)-4-OXOBUTOXI)-N-METILBENZAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DEL RECEPTOR DE QUIMIOQUINA CCR1 SIENDO UTILES EN EL TRATAMIENTO DE ARTRITIS REUMATOIDE, ASMA ALERGICA, FIBROSIS PULMONAR, GLOMERULONEFRITIS, ATEROSCLEROSIS
PE2006000656A 2005-06-14 2006-06-12 Derivados n-amida de 8-azabiciclo[3.2.1]oct-3-ilo como antagonistas de ccr1 PE20070017A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES200501431A ES2277745B1 (es) 2005-06-14 2005-06-14 Derivados n-amida de 8-azabiciclo /3.2.1/oct-3-ilo como antagonistas de ccr1.

Publications (1)

Publication Number Publication Date
PE20070017A1 true PE20070017A1 (es) 2007-02-05

Family

ID=35740673

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2006000656A PE20070017A1 (es) 2005-06-14 2006-06-12 Derivados n-amida de 8-azabiciclo[3.2.1]oct-3-ilo como antagonistas de ccr1

Country Status (12)

Country Link
US (1) US20090130090A1 (es)
EP (1) EP1891064B1 (es)
JP (1) JP2008543795A (es)
CN (1) CN101228158A (es)
AR (1) AR057651A1 (es)
AT (1) ATE441647T1 (es)
DE (1) DE602006008937D1 (es)
ES (2) ES2277745B1 (es)
PE (1) PE20070017A1 (es)
TW (1) TW200716626A (es)
UY (1) UY29572A1 (es)
WO (1) WO2006133802A1 (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007102768A1 (en) * 2006-03-07 2007-09-13 Astrazeneca Ab Piperidine derivatives, their process for preparation, their use as therapeutic agents and pharmaceutical compositions containing them .
NZ599853A (en) 2008-04-11 2012-08-31 Janssen Pharmaceutica Nv Process for the preparation of meso-N-[(3-endo)-8-benzyl-8-azabicyclo[3.2.1]oct-3-yl]acetamide and its derivatives
WO2010091104A1 (en) * 2009-02-06 2010-08-12 Exelixis, Inc. Glucosylceramide synthase inhibitors
EP2430019B1 (en) 2009-05-14 2013-09-18 Janssen Pharmaceutica, N.V. Compounds with two fused bicyclic heteroaryl moieties as modulators of leukotriene a4 hydrolase
US8697691B2 (en) * 2009-12-21 2014-04-15 Vanderbilt University Alkyl 3-((2-amidoethyl)amino)-8-azabicyclo[3.2.1]octane-8-carboxylate analogs as selective M1 agonists and methods of making and using same
EP2771484A1 (en) 2011-10-28 2014-09-03 Galderma Research & Development New leukocyte infiltrate markers for rosacea and uses thereof
EP2875023B1 (en) * 2012-07-19 2017-04-05 Janssen Pharmaceutica NV Octahydro-cyclopentapyrrolyl antagonists of ccr2

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6140338A (en) * 1996-07-29 2000-10-31 Banyu Pharmaceutical, Co., Ltd. Chemokine receptor antagonists
PE20001420A1 (es) * 1998-12-23 2000-12-18 Pfizer Moduladores de ccr5
SE0200919D0 (sv) * 2002-03-25 2002-03-25 Astrazeneca Ab Chemical compounds
BR0312699A (pt) * 2002-07-18 2005-04-26 Pfizer Prod Inc Derivados de piperidina bicìclica como antagonistas de receptor de quimiocina ccr1
SE0301369D0 (sv) * 2003-05-09 2003-05-09 Astrazeneca Ab Chemical compounds

Also Published As

Publication number Publication date
JP2008543795A (ja) 2008-12-04
CN101228158A (zh) 2008-07-23
ES2277745A1 (es) 2007-07-16
EP1891064B1 (en) 2009-09-02
DE602006008937D1 (de) 2009-10-15
UY29572A1 (es) 2006-12-29
ATE441647T1 (de) 2009-09-15
US20090130090A1 (en) 2009-05-21
ES2332819T3 (es) 2010-02-12
AR057651A1 (es) 2007-12-12
WO2006133802A1 (en) 2006-12-21
EP1891064A1 (en) 2008-02-27
ES2277745B1 (es) 2008-06-01
TW200716626A (en) 2007-05-01

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