CO5160241A1 - 2-aminopiridinas que contienen sustituyentes de tipo anillo condensado - Google Patents

2-aminopiridinas que contienen sustituyentes de tipo anillo condensado

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Publication number
CO5160241A1
CO5160241A1 CO00012733A CO00012733A CO5160241A1 CO 5160241 A1 CO5160241 A1 CO 5160241A1 CO 00012733 A CO00012733 A CO 00012733A CO 00012733 A CO00012733 A CO 00012733A CO 5160241 A1 CO5160241 A1 CO 5160241A1
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Colombia
Prior art keywords
group
ring
alkyl
aryl
aralkyl
Prior art date
Application number
CO00012733A
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English (en)
Inventor
Lowe Iii John Adams
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Pfizer Prod Inc
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Publication date
Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of CO5160241A1 publication Critical patent/CO5160241A1/es

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    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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 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
    • C07D213/72Nitrogen atoms
    • C07D213/73Unsubstituted amino or imino radicals
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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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links

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Abstract

La presente invención se refiere a derivados de 2-aminopiridina de la fórmula I:<EMI FILE="00012733_1" ID="1" IMF=JPEG >o sales farmacéuticamente aceptables de los mismos, en la que A y B son cada uno independientemente H, o juntos, A y B forman un anillo condensado al anillo de fenilo, siendo dicho anillo saturado o insaturado y contenido de 5 a 7 átomos en el anillo, donde dichos átomos en el anillo pueden opcionalmente comprender de 1 a 2 heteroátomos seleccionados independientemente del grupo constituido por N, O o S, siempre que los mismos de dos anillos adyacentes no sean heteroátomos; X es oxigeno o un enlace sencillo; Y es alquilo (C1-C6); R1 es hidrógeno, alquilo (C1-C6) o un grupo (alquilo C1-C6) sustituido con -NR2R3 en el que R2 y R3 se seleccionan bien independientemente del grupo constituido por H, alquilo, arilo, aralquilo o tetrahidronaftaleno, siendo dicho grupo arilo o dicho resto arilo de dicho grupo aralquilo fenilo o naftilo, conteniendo dicho grupo alquilo o dicho resto alquilo de dicho grupo aralquilo de uno a seis átomos de carbono y siendo una cadena lineal o ramificada, y estando dicho grupo arilo, dicho tetrahidronaftaleno o dicho resto arilo de dicho grupo aralquilo opcionalmente sustituido con uno a tres restos de halógeno, nitro, ciano, amino, alcoxi (C1-C4) y alquilamino (C1-C4), o bien R2 y R3 forman, junto con un nitrógeno al que están unidos, un anillo heterocíclíco, o un anillo cíclico o bicíclico que está saturado o insaturado. Los compuestos de la invención tienen la capacidad de inhibir la actividad de las síntasas de óxido nítrico (NOS), y por lo tanto, son útiles en el tratamiento de enfermedades, estados y trastornos del sistema nervioso central, entre otros.
CO00012733A 1999-02-25 2000-02-23 2-aminopiridinas que contienen sustituyentes de tipo anillo condensado CO5160241A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US12159799P 1999-02-25 1999-02-25

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CO5160241A1 true CO5160241A1 (es) 2002-05-30

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CO00012733A CO5160241A1 (es) 1999-02-25 2000-02-23 2-aminopiridinas que contienen sustituyentes de tipo anillo condensado

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US (2) US6211208B1 (es)
EP (1) EP1155000B1 (es)
JP (1) JP3825636B2 (es)
KR (1) KR20010114213A (es)
CN (1) CN1341099A (es)
AP (1) AP2001002251A0 (es)
AR (1) AR018979A1 (es)
AT (1) ATE245143T1 (es)
AU (1) AU767593B2 (es)
BG (1) BG105855A (es)
BR (1) BR0008569A (es)
CA (1) CA2364719C (es)
CO (1) CO5160241A1 (es)
CR (1) CR6438A (es)
CZ (1) CZ20013036A3 (es)
DE (1) DE60003893T2 (es)
DK (1) DK1155000T3 (es)
DZ (1) DZ3017A1 (es)
EA (1) EA003941B1 (es)
EE (1) EE200100454A (es)
ES (1) ES2200813T3 (es)
GT (1) GT200000021A (es)
HN (1) HN2000000016A (es)
HR (1) HRP20010597A2 (es)
HU (1) HUP0200163A3 (es)
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IL (1) IL144308A0 (es)
IS (1) IS6005A (es)
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NO (1) NO20014095L (es)
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PA (1) PA8490901A1 (es)
PE (1) PE20001482A1 (es)
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SV (1) SV2002000026A (es)
TN (1) TNSN00034A1 (es)
TR (1) TR200102481T2 (es)
WO (1) WO2000050400A1 (es)
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US20010049379A1 (en) * 1997-08-27 2001-12-06 Lowe John Adams 2-aminopyridines containing fused ring substituents
TR200102481T2 (tr) * 1999-02-25 2002-01-21 Pfizer Products Inc. Fazlı zincir muadili içeren 2-aminopiridinler.
KR20020084278A (ko) 2000-03-31 2002-11-04 코센시스 인크 항경련제 및 나트륨 통로 차단제로서의 아미노피리딘과이의 용도
US20040092741A1 (en) * 2002-11-08 2004-05-13 Pfizer Inc Substituted pyridines via boronic acid coupling
US8729107B2 (en) * 2002-12-06 2014-05-20 Purdue Research Foundation Pyridines for treating injured mammalian nerve tissue
EP1567497B1 (en) * 2002-12-06 2009-09-23 Purdue Research Foundation Pyridines for treating injured mammalian nerve tissue
US20050192321A1 (en) * 2003-09-15 2005-09-01 Meythaler Jay M. Treatment of neuropathy with rapid release aminopyridine
WO2014138460A1 (en) * 2013-03-07 2014-09-12 Northwestern University 2-aminopyridine-based selective neuronal nitric oxide synthase inhibitors
US9951014B2 (en) 2014-11-04 2018-04-24 Northwestern University Mammalian and bacterial nitric oxide synthase inhibitors
US10759791B2 (en) 2014-11-04 2020-09-01 Northwestern University Mammalian and bacterial nitric oxide synthase inhibitors
US9585867B2 (en) 2015-08-06 2017-03-07 Charles Everett Ankner Cannabinod formulation for the sedation of a human or animal

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AU4515696A (en) * 1994-12-12 1996-07-03 Merck & Co., Inc. Substituted 2-aminopyridines as inhibitors of nitric oxide synthase
JPH101435A (ja) * 1995-09-14 1998-01-06 Nippon Kayaku Co Ltd 2−アミノピリジン類を有効成分とする一酸化窒素合成酵素阻害剤
DK0891332T3 (da) * 1996-03-29 2004-07-05 Pfizer 6-phenylpyridyl-2-aminderivater
HN1997000027A (es) 1996-12-06 1997-06-05 Pfizer Prod Inc Derivados de 6-fenil piridil - 2 amina
JP3505189B2 (ja) * 1997-02-10 2004-03-08 ファイザー・プロダクツ・インク 2−アミノ−6−(2−置換−4−フェノキシ)−置換ピリジン
HN1998000118A (es) * 1997-08-27 1999-02-09 Pfizer Prod Inc 2 - aminopiridinas que contienen sustituyentes de anillos condensados.
HN1998000125A (es) * 1997-08-28 1999-02-09 Pfizer Prod Inc 2-aminopiridinas con sustituyentes alcoxi ramificados
SK17912000A3 (sk) * 1998-06-03 2001-09-11 Pfizer Products Inc. 2-aminopyridny obsahujce kondenzovan cyklick substituenty ako inhibtory syntzy oxidu dusnatho
TR200102481T2 (tr) * 1999-02-25 2002-01-21 Pfizer Products Inc. Fazlı zincir muadili içeren 2-aminopiridinler.

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BG105855A (en) 2002-04-30
ZA200106974B (en) 2002-10-14
PA8490901A1 (es) 2001-04-30
IL144308A0 (en) 2002-05-23
JP2002537381A (ja) 2002-11-05
ATE245143T1 (de) 2003-08-15
NO20014095L (no) 2001-10-24
YU58301A (sh) 2004-05-12
GT200000021A (es) 2001-08-17
PE20001482A1 (es) 2001-01-03
HUP0200163A3 (en) 2002-11-28
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SK12022001A3 (sk) 2002-07-02
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AU2124300A (en) 2000-09-14
TR200102481T2 (tr) 2002-01-21
IS6005A (is) 2001-07-13
TNSN00034A1 (fr) 2005-11-10
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KR20010114213A (ko) 2001-12-31
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CN1341099A (zh) 2002-03-20
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