ES2545352T3 - Derivados de la furopiridina - Google Patents

Derivados de la furopiridina Download PDF

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ES2545352T3
ES2545352T3 ES11738631T ES11738631T ES2545352T3 ES 2545352 T3 ES2545352 T3 ES 2545352T3 ES 11738631 T ES11738631 T ES 11738631T ES 11738631 T ES11738631 T ES 11738631T ES 2545352 T3 ES2545352 T3 ES 2545352T3
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mono
atoms
unsubstituted
nhet3
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Lars Burgdorf
Melanie Schultz
Tatjana Ross
Brian Hodous
Justin Potnick
Amanda E. Sutton
Bayard R. Huck
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Merck Patent GmbH
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Merck Patent GmbH
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
    • AHUMAN NECESSITIES
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    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4355Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
    • AHUMAN NECESSITIES
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    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
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    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
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    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53831,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

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  • Health & Medical Sciences (AREA)
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  • Physical Education & Sports Medicine (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Compuestos de la fórmula I **Fórmula** donde R1 designa Ar1 o Het1, R2 designa Ar2, Het2, NH(CH2)nAr2, O(CH2)nAr2 o NH(CH2)nHet2, Ar1 designa fenilo, naftilo o bifenilo, cada uno de ellos no-sustituido o mono-, di- o trisustituído por Hal, A, O(CH2)pCyc, Alk, (CH2)nOH, (CH2)nOA, (CH2)nCOOH, (CH2)nCOOA, S(O)mA, fenoxi, benciloxi, (CH2)nNH2, (CH2)nNHA, (CH2)nNA2, [C(R3)2]nCN, NO2, (CH2)nCONH2, (CH2)nCONHA, (CH2)nCONA2, SO2NH2, SO2NHA, SO2NA2, NHCONH2, (CH2)nNHCOA, (CH2)nNHCOAlk, NHCOCH>=CH(CH2)pNA2, CHO, COA, SO3H, 10 O(CH2)pNH2, O(CH2)pNHCOOA, O(CH2)pNHA, O(CH2)pNA2, NH(CH2)pNH2, NH(CH2)pNHCOOA, NH(CH2)pNHA, NH(CH2)pNA2, NHCOHet3, COHet3, (CH2)nHet3 O(CH2)nHet3 y/o O(CH2)nCH(OH)(CH2), Ar2 designa fenilo, naftilo o bifenilo, cada uno de ellos no-sustituido o mono-, di- o trisustituído por Hal, A, (CH2)nOH, (CH2)nOA, O(CH2)pCyc, OAr3, benciloxi, (CH2)nCOOH, (CH2)nCOOA, S(O)mA, (CH2)nNH2, (CH2)nNHA, (CH2)nNA2, [C(R3]nCN, NO2, CONH(CH2)pNH2, CONH(CH2)pNHA, CONH(CH2)pNA2, CONH(CH2)pOA, CONH(CH2)pOH, (CH2)nCONH2, (CH2)nCONHA, (CH2)nCONA2, SO2NH2, SO2NHA, SO2NA2, NHCONH2, (CH2)nNHCOA, (CH2)nNHCOAlk, CHO, COA, SO3H, O(CH2)pNH2, O(CH2)pNHA, O(CH2)pNA2, CONHAr3, NHCOAr3, CONH(CH2)nHet3, NHCOHet3, COHet3, (CH2)nHet3, S(CH2)nHet3 y/o O(CH2)nHet3, Het1 designa un heterociclo mono- o bicíclico aromático teniendo 1 a 4 átomos de N, O y/o S, que puede ser no-sustituido o mono- o disustituído por A, bencilo, Het4, OH y/o OA, Het2 designa un heterociclo mono- o bicíclico saturado, insaturado o aromático teniendo 1 a 4 átomos de N, O y/o S, que puede ser no-sustituido o mono-, di-, tri- o tetrasustituido por Hal, A, (CH2)nHet4, OHet4, NH(CH2)nHet4, (CH2)nCOOH, (CH2)nCOOA, fenilo, bencilo, CHO, COA, (CH2)nNH2, (CH2)nNHA, (CH2)nNA2, CN, (CH2)nOH, (CH2)nOA, (CH2)pCH(OH)(CH2)pOH, (CH2)pCH(OH)(CH2)pOA, NH(CH2)pNH2, NHSO2, NASO2A, SO2A y/o >=O, Het3 designa a mono- o bicíclico saturados, insaturados o aromático heterociclo teniendo 1 a 4 N, O y/o S átomos, que puede ser no-sustituido o mono-, di-, tri- o tetrasustituido por A, Hal, (CH2)nNH2, (CH2)nNHA, (CH2)nNA2, (CH2)nOH, (CH2)nOA, COOA, Ar3 y/o >=O, Het4 designa un heterociclo monocíclico saturado, insaturado o aromático teniendo 1 a 4 átomos de N, O y/o S, que puede ser no-sustituido o mono-, di- o trisustituído por A, R3 designa H o alquilo teniendo 1, 2, 3 o 4 átomos de C, A designa alquilo no-ramificado o ramificado teniendo 1-10 átomos de C, donde 1-7 átomos de H pueden reemplazarse por F y/o Cl y/o donde uno o dos grupos CH2 no-adyacentes pueden reemplazarse por grupos O, NH, S, SO, SO2 y/o CH>=CH, o alquilo cíclico teniendo 3-7 átomos de C, que puede estar no-sustituido o monosustituído por OH, NHCOOA o NH2, Cyc designa alquilo cíclico teniendo 3-7 átomos de C, Alk designa alquenilo o alquinilo teniendo 2, 3, 4, 5 ó 6 átomos de C, Ar3 designa fenilo, no sustituido o mono-, di- o trisustituído por Hal y/o A, Hal designa F, Cl, Br ó I, m designa 0, 1 ó 2, n designa 0, 1, 2, 3 ó 4, p designa 1, 2, 3 ó 4, 5 y solvatos, sales, tautómeros y estereoisómeros farmacéuticamente aceptables de estos.
ES11738631T 2010-08-27 2011-07-29 Derivados de la furopiridina Active ES2545352T3 (es)

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Application Number Priority Date Filing Date Title
EP10008928 2010-08-27
EP10008928 2010-08-27
PCT/EP2011/003831 WO2012025187A2 (en) 2010-08-27 2011-07-29 Furopyridine derivatives

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ES2545352T3 true ES2545352T3 (es) 2015-09-10

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US (1) US9006440B2 (es)
EP (1) EP2609100B1 (es)
JP (1) JP5789300B2 (es)
KR (1) KR20130108318A (es)
CN (1) CN103052640B (es)
AR (1) AR082727A1 (es)
AU (1) AU2011295441B2 (es)
BR (1) BR112013004624A2 (es)
CA (1) CA2809333C (es)
EA (1) EA201300283A1 (es)
ES (1) ES2545352T3 (es)
IL (1) IL224870A (es)
MX (1) MX2013002199A (es)
SG (1) SG187956A1 (es)
WO (1) WO2012025187A2 (es)

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EP3942045A1 (en) 2019-03-21 2022-01-26 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
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WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
MX2022013619A (es) 2020-05-01 2022-11-16 Gilead Sciences Inc Compuestos de 2,4-dioxopirimidina que inhiben cd73.
WO2024033280A1 (en) 2022-08-09 2024-02-15 Merck Patent Gmbh Furopyridin and furopyrimidin, inhibitors of pi4k, for use in the treatment of parasite infection and malaria
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IL224870A (en) 2016-05-31
AU2011295441A1 (en) 2013-04-11
CA2809333C (en) 2018-09-25
MX2013002199A (es) 2013-03-18
BR112013004624A2 (pt) 2016-07-05
AR082727A1 (es) 2012-12-26
SG187956A1 (en) 2013-03-28
US9006440B2 (en) 2015-04-14
JP2013536208A (ja) 2013-09-19
EP2609100A2 (en) 2013-07-03
AU2011295441B2 (en) 2015-04-09
WO2012025187A2 (en) 2012-03-01
EP2609100B1 (en) 2015-06-24
CN103052640A (zh) 2013-04-17
CA2809333A1 (en) 2012-03-01
WO2012025187A3 (en) 2012-06-21
CN103052640B (zh) 2017-06-30
US20130225569A1 (en) 2013-08-29
EA201300283A1 (ru) 2013-08-30
KR20130108318A (ko) 2013-10-02
JP5789300B2 (ja) 2015-10-07

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