AR066938A1 - Derivados de 4-piridin-2-pirimidinil amino, una composicion fungicida que los comprende y un metodo para controlar los hongos fitopatogenicos de los cultivos que los emplea. - Google Patents
Derivados de 4-piridin-2-pirimidinil amino, una composicion fungicida que los comprende y un metodo para controlar los hongos fitopatogenicos de los cultivos que los emplea.Info
- Publication number
- AR066938A1 AR066938A1 ARP080102460A ARP080102460A AR066938A1 AR 066938 A1 AR066938 A1 AR 066938A1 AR P080102460 A ARP080102460 A AR P080102460A AR P080102460 A ARP080102460 A AR P080102460A AR 066938 A1 AR066938 A1 AR 066938A1
- Authority
- AR
- Argentina
- Prior art keywords
- unsubstituted
- substituted
- alkyl
- halogen atoms
- group
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 2
- 230000003032 phytopathogenic effect Effects 0.000 title abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 37
- -1 formyloxy group Chemical group 0.000 abstract 19
- 125000000217 alkyl group Chemical group 0.000 abstract 14
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 11
- 125000001188 haloalkyl group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 10
- 125000003545 alkoxy group Chemical group 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 4
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 3
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 2
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 abstract 1
- BYGMGMFGEVNKSJ-UHFFFAOYSA-N 4-[2-(ethylamino)pyridin-4-yl]-n-(5-piperazin-1-ylpyridin-2-yl)pyrimidin-2-amine Chemical compound C1=NC(NCC)=CC(C=2N=C(NC=3N=CC(=CC=3)N3CCNCC3)N=CC=2)=C1 BYGMGMFGEVNKSJ-UHFFFAOYSA-N 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 239000002184 metal Chemical class 0.000 abstract 1
- 229910052752 metalloid Inorganic materials 0.000 abstract 1
- 150000002738 metalloids Chemical class 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/14—Heterocyclic 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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Se proveen además composiciones fungicidas y métodos para combatir hongos fitopatogénicos que los emplea Reivindicacion 1: Un compuesto de formula (1): en la que Het representa un heterociclo saturado o insaturado, aromático o no aromático de 4, 5, 6 o 7 elementos que comprende hasta cuatro heteroátomos que pueden ser iguales o diferentes; Y independientemente representa un átomo de halogeno, un grupo nitro, un grupo hidroxi, un grupo oxo, un grupo ciano, un grupo amino, un grupo sulfenilo, un grupo pentafluoro-lambda6-sulfenilo, un grupo formilo, un grupo formiloxi, un grupo formilamino, un grupo carbamoílo, un grupo N-hidroxicarbamoílo, un grupo carbamato, un grupo (hidroxiimino)-alquil C1-6, un alquilo C1-8, un tri(alquil C1-8)sililo, un tri(alquil C1-8)silil-alquil C1-8 sustituido o no sustituido, un cicloalquilo C1-8 sustituido o no sustituido, tri(alquil C1-8)silil-cicloalquil C1-8 sustituido o no sustituido, un halogenoalquil C1-8 que tiene 1 a 5 átomos de halogeno, un halogenocicloalquilo C1-8 que tiene 1 a 5 átomos de halogeno, un alquenilo C2-8, un alquinilo C2-8, un alquenil C2-8-oxi, un alquinil C2-8-oxi, un alquil C1-8-amino, un di-alquil C1-8-amino, un alcoxi C1-8, un halogenoalcoxi C1-8 que tiene 1 a 5 átomos de halogeno, un alquil C1-8-sulfenilo, un halogenoalquil C1-8-sulfenilo que tiene 1 a 5 átomos de halogeno, un alquenil C2-8-oxi, un halogenoalquenil C2-8-oxi que tiene 1 a 5 átomos de halogeno, un alquinil C3-8-oxi, un halogenoalquinil C3-8-oxi que tiene 1 a 5 átomos de halogeno, un alquil C1-8carbonilo, un halogenoalquil C1-8-carbonilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-carbamoílo, un di-alquil C1-8-carbamoílo, un alquil N-C1-8-oxicarbamoílo, un alcoxi C1-8-carbamoílo, un N-alquil C1-8-alcoxi C1-8-carbamoílo, un alcoxi C1-8-carbonilo, un halogenoalcoxi C1-8-carbonilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-carboniloxi, un halogenoalquil C1-8-carboniloxi que tiene 1 a 5 átomos de halogeno, un alquil C1-8-carbonilamino, un halogenoalquil C1-8-carbonilamino que tiene 1 a 5 átomos de halogeno, un alquil C1-8-aminocarboniloxi, un di-alquil C1-8-aminocarboniloxi, un alquil C1-8-oxicarboniloxi, un alquil C1-8-sulfenilo, un halogenoalquil C1-8-sulfenilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-sulfinilo, un halogenoalquil C1-8-sulfinilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-sulfonilo, un halogenoalquil C1-8-sulfonilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-aminosulfamoílo, un dialquil C1-8-aminosulfamoílo, un (alcoxi C1-6-imino)-alquil C1-6, un alquenil (C1-6-oxiimino)-alquil C1-6, un alquinil (C1-6-oxiimino)-alquil C1-6, un 2-oxopirrolidin-1-ilo, (benciloxiimino)-alquil C1-6 sustituido o no sustituido, alcoxialquil C1-8 sustituido o no sustituido, halogenoalcoxialquilo C1-8 sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, benciloxi sustituido o no sustituido, bencilsulfenilo sustituido o no sustituido, bencilamino sustituido o no sustituido, fenoxi sustituido o no sustituido, fenilsulfenilo sustituido o no sustituido o fenilamino sustituido o no sustituido; p representa 0, 1, 2, 3, 4, 5 o 6; Ra representa un átomo de hidrogeno, un grupo ciano, un grupo formilo, un grupo formiloxi, un alcoxi C1-8-carbonilo, un halogenoalcoxi C1-8-carbonilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-carbonilo, un halogenoalquil C1-8-carbonilo que tiene 1 a 5 átomos de halogeno, un alquil C1-8-sulfonilo, un halogenoalquil C1-8-sulfonilo que tiene 1 a 5 átomos de halogeno, un alquilo C1-8, un cicloalquilo C1-8, un halogenoalquilo C1-8 que tiene 1 a 5 átomos de halogeno, un halogenocicloaquilo C1-8 que tiene 1 a 5 átomos de halogeno, un alquenilo C2-8, un alquinilo C2-8, un alcoxialquilo C1-8, un halogenoalcoxialquilo C1-8 que tiene 1 a 5 átomos e halogeno; Rb y Rc independientemente representan un átomo de hidrogeno, un átomo de halogeno, un ciano, un alquilo C1-8, un cicloalquilo C1-8, un halogenoalquilo C1-8 que tiene 1 a 5 átomos de halogeno, un halogenocicloalquilo C1-8 que tiene 1 a 5 átomos de halogeno; X independientemente representa un alquilo C1-10, un halogenoalquilo C1-10, un átomo de halogeno o un ciano; n representa 0,1,2 o 3; L1 y L2 independientemente representan un átomo de hidrogeno, un grupo ciano, un grupo hidroxi, un grupo amino, un grupo formilo, un grupo formiloxi, un grupo formilamino, un grupo carbamoilo, un grupo N-hidroxicarbamoílo, un grupo carbamato, un grupo (hidroxiimino)-alquil C1-6 sustituido o no sustituido, alquilo C1-8-sustituido o no sustituido, tri( alquil C1-8-)sililo, tri(alquil C1-8)silil-alquil C1-8 sustituido o no sustituido, cicloalquilo C1-8 sustituido o no sustituido, tri(alquil C1-8)silil-cicloalquil C1-8 sustituido o no sustituido, halogenoalquil C1-8 sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, halogenocicloalquil C1-8 sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, un alquenilo C2-8, alquinilo C2-8 sustituido o no sustituido, alquilamino C1-8 sustituido o no sustituido, di-alquil C1-8-amino sustituido o no sustituido, alcoxi C1-8 sustituido o no sustituido, halogenoalcoxi C1-8 sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquenil C2-8-oxi sustituido o no sustituido, alquinil C2-8-oxi sustituido o no sustituido, alquenil C2-8-oxi sustituido o no sustituido, halogenoalquenil C2-8-oxi sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquinil C3-8-oxi sustituido o no sustituido, halogenoalquinil C3-8-oxi sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-carbonilo sustituido o no sustituido, halogenoalquil C1-8-carbonilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-carbamoílo sustituido o no sustituido, dialquil C1-8-carbamoílo sustituido o no sustituido, N-alquil C1-8-oxicarbamoílo sustituido o no sustituido, alcoxi C1-8-carbamoílo sustituido o no sustituido, N-alquil C1-8-alcoxi C1-8-carbamoílo sustituido o no sustituido, alcoxi C1-8-carbonilo sustituido o no sustituido, halogenoalcoxi C1-8-carbonilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-carboniloxi sustituido o no sustituido, halogenoalquil C1-8-carboniloxi sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-carbonilamino sustituido o no sustituido, halogenoalquil C1-8-carbonilamino sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-aminocarboniloxi sustituido o no sustituido, di-alquil C1-8-aminocarboniloxi sustituido o no sustituido, alquil C1-8-oxicarboniloxi sustituido o no sustituido, alquil C1-8-sulfenilo sustituido o no sustituido, halogenoalquil C1-8-sulfenilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-sulfinilo sustituido o no sustituido, halogenoalquil C1-8-sulfinilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-sulfonilo sustituido o no sustituido, halogenoalquil C1-8-sulfonilo sustituido o no sustituido que tiene 1 a 5 átomos de halogeno, alquil C1-8-aminosulfamoílo sustituido o no sustituido, di-alquil C1-8-aminosulfamoílo sustituido o no sustituido, (alcoxi C1-6-imino)-alquil C1-6 sustituido o no sustituido, (alquenil C1-6-oxiimino)-alquil C1-6 sustituido o no sustituido, (alquinil C1-6-oxiimino)-alquil C1-6 sustituido o no sustituido, (2-oxopirrolidin-1-il) alquil C1-8, (2-oxopirrolidin-1-il) halogenoalquil C1-8 que tiene 1 a 5 átomos de halogeno, (2-oxopiperidin-1-il) alquil C1-8, (2-oxopiperidin-1-il) halogenoalquil C1-8 que tiene 1 a 5 átomos de halogeno, (2-oxoazepan-1-il) alquil C1-8,(2-oxoazepan-1-il) halogenoalquil C1-8 que tiene 1 a 5 átomos de halogeno, (benciloxiimino)-alquil C1-6 sustituido o no sustituido; L1 y L2 pueden formar conjuntamente un heterociclo que incluye N, de 4, 5, 6 o 7 elementos, sustituido o no sustituido, aromático o no aromático, saturado o insaturado, que comprende hasta 4 heteroátomos seleccionados independientemente en la lista consistente en N, O, S; así como sales, N-oxidos, complejos metálicos, complejos metaloides y sus isomeros opticamente activos o geométricos; con la condicion de que esté excluido el compuesto siguiente: 4-[2-(etilamino)-4-piridinil]-N-[5-(-piperazinil)-2-piridinil]-2-pirimidinamina.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07356077 | 2007-06-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR066938A1 true AR066938A1 (es) | 2009-09-23 |
Family
ID=38912671
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP080102460A AR066938A1 (es) | 2007-06-08 | 2008-06-09 | Derivados de 4-piridin-2-pirimidinil amino, una composicion fungicida que los comprende y un metodo para controlar los hongos fitopatogenicos de los cultivos que los emplea. |
Country Status (17)
Country | Link |
---|---|
US (1) | US8273759B2 (es) |
EP (1) | EP2164841A1 (es) |
JP (1) | JP2010529959A (es) |
KR (1) | KR20100020454A (es) |
CN (1) | CN101679376A (es) |
AR (1) | AR066938A1 (es) |
AU (1) | AU2008258508A1 (es) |
BR (1) | BRPI0809896A2 (es) |
CA (1) | CA2685588A1 (es) |
CL (1) | CL2008001693A1 (es) |
CO (1) | CO6270256A2 (es) |
IL (1) | IL201623A0 (es) |
MX (1) | MX2009013262A (es) |
RU (1) | RU2471793C2 (es) |
TW (1) | TW200911780A (es) |
WO (1) | WO2008148889A1 (es) |
ZA (1) | ZA200907610B (es) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011503006A (ja) | 2007-11-06 | 2011-01-27 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 殺菌性複素環アミン |
BRPI0916056A2 (pt) * | 2008-11-13 | 2015-08-11 | Bayer Cropscience Ag | Derivado de piridilazinilamino, composto, uso de um composto, composição fungicida, método de controle dos fungos fitopatogênicos de safras e método de combate a fungos fitopatogênicos e produtores de micotoxinas |
EP3075730B1 (en) | 2010-06-04 | 2018-10-24 | Genentech, Inc. | Aminopyrimidine derivatives as lrrk2 modulators |
TW201302733A (zh) | 2010-11-10 | 2013-01-16 | Hoffmann La Roche | 作為lrrk2調節劑之吡唑胺基嘧啶衍生物 |
WO2012101065A2 (en) * | 2011-01-28 | 2012-08-02 | Novartis Ag | Pyrimidine biaryl amine compounds and their uses |
WO2013106614A1 (en) | 2012-01-13 | 2013-07-18 | Bristol-Myers Squibb Company | Triazolyl-substituted pyridyl compounds useful as kinase inhibitors |
WO2013106612A1 (en) | 2012-01-13 | 2013-07-18 | Bristol-Myers Squibb Company | Heterocyclic-substituted pyridyl compounds useful as kinase inhibitors |
ES2575604T3 (es) | 2012-01-13 | 2016-06-29 | Bristol-Myers Squibb Company | Compuestos de piridilo sustituidos con tiazolilo o tiadiazolilo útiles como inhibidores cinasa |
UA116774C2 (uk) | 2012-03-01 | 2018-05-10 | Еррей Біофарма Інк. | Інгібітори серин/треонінкінази |
US9657009B2 (en) | 2012-11-08 | 2017-05-23 | Bristol-Myers Squibb Company | Heteroaryl substituted pyridyl compounds useful as kinase modulators |
EP2922840B1 (en) | 2012-11-08 | 2016-12-21 | Bristol-Myers Squibb Company | Bicyclic heterocycle substituted pyridyl compounds useful as kinase modulators |
UY35935A (es) | 2014-01-03 | 2015-06-30 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | Compuestos de nicotinamida sustituida con heteroarilo como inhibidores de quinasa y moduladores de irak-4 |
US10294229B2 (en) | 2015-06-24 | 2019-05-21 | Bristol-Myers Squibb Company | Heteroaryl substituted aminopyridine compounds |
UY36747A (es) | 2015-06-24 | 2016-12-30 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | Compuestos de aminopiridina sustituida con heteroarilo como inhibidores de quinasa y modulantes de irak-4 y composiciones farmacéuticas que los contienen |
JP6720355B2 (ja) | 2015-06-24 | 2020-07-08 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | ヘテロアリール置換のアミノピリジン化合物 |
HUE056493T2 (hu) | 2017-05-11 | 2022-02-28 | Bristol Myers Squibb Co | Tienopiridinek és benzotiofének, amelyek hasznosak IRAK4 inibitorokként |
Family Cites Families (8)
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EP1019366B1 (de) * | 1995-12-27 | 2002-03-13 | Basf Aktiengesellschaft | Iminooxyphenylessigsäurederivate, verfahren und zwischenprodukte zu ihrer herstellung und ihre verwendung |
EP1254903B1 (en) * | 2001-04-20 | 2005-06-08 | Ciba SC Holding AG | 4-Amino-2-(pyridin-2-yl)pyrimidine as microbicidal active substances |
GB0123589D0 (en) * | 2001-10-01 | 2001-11-21 | Syngenta Participations Ag | Organic compounds |
GB0129476D0 (en) | 2001-12-10 | 2002-01-30 | Syngenta Participations Ag | Organic compounds |
ATE433967T1 (de) * | 2003-01-17 | 2009-07-15 | Warner Lambert Co | 2-aminopyridin-substituierteheterocyclen als inhibitoren der zellulären proliferation |
GB0307268D0 (en) | 2003-03-28 | 2003-05-07 | Syngenta Ltd | Organic compounds |
US6969726B2 (en) * | 2003-06-03 | 2005-11-29 | Rib X Pharmaceuticals Inc | Biaryl heterocyclic compounds and methods of making and using the same |
ES2229928B1 (es) * | 2003-10-02 | 2006-07-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de pirimidin-2-amina. |
-
2008
- 2008-06-06 WO PCT/EP2008/057126 patent/WO2008148889A1/en active Application Filing
- 2008-06-06 KR KR1020097024533A patent/KR20100020454A/ko not_active Application Discontinuation
- 2008-06-06 CN CN200880019145A patent/CN101679376A/zh active Pending
- 2008-06-06 EP EP08760695A patent/EP2164841A1/en not_active Withdrawn
- 2008-06-06 AU AU2008258508A patent/AU2008258508A1/en not_active Abandoned
- 2008-06-06 US US12/451,941 patent/US8273759B2/en not_active Expired - Fee Related
- 2008-06-06 JP JP2010510826A patent/JP2010529959A/ja not_active Withdrawn
- 2008-06-06 RU RU2009149497/04A patent/RU2471793C2/ru not_active IP Right Cessation
- 2008-06-06 CA CA002685588A patent/CA2685588A1/en not_active Abandoned
- 2008-06-06 BR BRPI0809896-4A2A patent/BRPI0809896A2/pt not_active Application Discontinuation
- 2008-06-06 MX MX2009013262A patent/MX2009013262A/es not_active Application Discontinuation
- 2008-06-09 TW TW097121437A patent/TW200911780A/zh unknown
- 2008-06-09 AR ARP080102460A patent/AR066938A1/es not_active Application Discontinuation
- 2008-06-09 CL CL2008001693A patent/CL2008001693A1/es unknown
-
2009
- 2009-10-19 IL IL201623A patent/IL201623A0/en unknown
- 2009-10-29 ZA ZA200907610A patent/ZA200907610B/xx unknown
-
2010
- 2010-01-07 CO CO10001461A patent/CO6270256A2/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
KR20100020454A (ko) | 2010-02-22 |
JP2010529959A (ja) | 2010-09-02 |
US8273759B2 (en) | 2012-09-25 |
EP2164841A1 (en) | 2010-03-24 |
CO6270256A2 (es) | 2011-04-20 |
CL2008001693A1 (es) | 2009-03-06 |
AU2008258508A1 (en) | 2008-12-11 |
ZA200907610B (en) | 2010-07-28 |
IL201623A0 (en) | 2010-05-31 |
CN101679376A (zh) | 2010-03-24 |
TW200911780A (en) | 2009-03-16 |
RU2471793C2 (ru) | 2013-01-10 |
CA2685588A1 (en) | 2008-12-11 |
BRPI0809896A2 (pt) | 2014-10-07 |
US20100204229A1 (en) | 2010-08-12 |
MX2009013262A (es) | 2010-01-25 |
WO2008148889A1 (en) | 2008-12-11 |
RU2009149497A (ru) | 2011-07-20 |
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