AR061888A1 - Herbicidas derivados de (1,2,4)-triazolo-(4,3-a)piridina - Google Patents
Herbicidas derivados de (1,2,4)-triazolo-(4,3-a)piridinaInfo
- Publication number
- AR061888A1 AR061888A1 ARP070103084A ARP070103084A AR061888A1 AR 061888 A1 AR061888 A1 AR 061888A1 AR P070103084 A ARP070103084 A AR P070103084A AR P070103084 A ARP070103084 A AR P070103084A AR 061888 A1 AR061888 A1 AR 061888A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- halogen
- haloalkyl
- cyano
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
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- 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)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Estos compuestos son adecuados para su uso como herbicidas. Reivindicacion 1: Un compuesto de formula (1) donde X1 es nitrogeno o CR1; X2 es nitrogeno si X1 es CR1 o es CR2 si X1 es nitrogeno; R1 y R2, independientemente entre sí, son hidrogeno, halogeno, hidroxi, mercapto, amino, azido, SF5, nitro, ciano, rodano, carbamoilo, carboxi, formilo, tri-alquil C1-4sililo, alquil C1-4-alcoxi C1-4fosfino o dialcoxi C1-4fosfono; o R1 y R2, independientemente entre sí, son un grupo -X6, -X5-X6 o -X4- X5-X6, donde X4 es alquileno C1-6, alquenileno C2-6 o alquinileno C2-6, que pueden estar mono- o polisustituidos con halogeno, hidroxi, alcoxi C1-6, cicloalcoxi C3-6, alcoxi C1-6-alcoxi C1-6, alcoxi C1-6-alcoxi C1-6-alcoxi C1-6 o alquilsulfoniloxi C1-2; o con un grupo alquileno C1-8 bivalente que puede estar interrumpido con 1 a 2 átomos de oxígeno, azufre o NRa26, donde dicho grupo alquileno C1-8 bivalente puede estar sustituido con sustituyentes del grupo que consta de halogeno, hidroxi, mercapto, amino, formilo, carboxi, nitro, ciano, carbamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6, haloalqueniloxi C2-6, ciano-alcoxi C1-6, alcoxi C1-6-alcoxi C1-6, alcoxi C1-6-alcoxi C1-6-alcoxi C1-6, alquiltio C1-6-alcoxi C1-6, alquilsulfinil C1-6-alcoxi C1-6, alquilsulfonil C1-6-alcoxi C1-6, alcoxi C1-6- carbonil-alcoxi C1-6, formiloxi, alquilcarboniloxi C1-6, alquilcarbonilo C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquiltio C1-6, haloalquilsulfinilo C1-6, haloalquilsulfonilo C1-6, alquiltiocarbonilo C1-6, alquilcarbonilo C1-6, di(alquil C1-6)amino, alquilsulfoniloxi C1-4, alquilcarbonilamino C1-4, N(alquil C1-4)-alquilcarbonilamino C1-4, alcoxicarbonilamino C1-4, N(alquil C1-4)-alcoxicarbonilamino C1-4, alquilsulfonilamino C1-4, N(alquil C1-4)- alquilsulfonilamino C1-4, OSO2-alquilo C1-4, rodano, tri-alquil C1-4sililo, alquil C1-4-alcoxi C1-4fosfino y dialcoxi C1-4fosfono; X5 es oxígeno, -OC(O)-, -OC(O)O-, -OC(O)N(R3)-, -ON(Ra21)-, -ON=C(Ra22)-, OS(O)2-, OS(O)2O-, OS(O)2N(R3)-, tio, sulfinilo, sulfonilo, -SO2N(R3)-, -S(O)2O-, -S(=NRa23)(O)-, -C(O)O-, -C(O)-, -C(O)N(R3)-, -C(Ra22)=NO-, -N(Ra21)o-, -N(R3)SO2-, -N(Ra24)-, -N(R3)C(O)-, -N(R3)C(O)O-, -N(R3)C(O)N(R3)-, -N(R3)SO2O-, -N(R3)SO2N(R3)-, -N=S(Ra25)(O)- o -S(Ra25)(O)=N-; X6 es alquilo C1-6, alquenilo C2-6 o alquinilo C2-6; o alquilo C1-6, alquenilo C2-6 o alquinilo C2-6 mono- o polisustituido con halogeno, hidroxi, mercapto, amino, formilo, carboxi, nitro, ciano, carbamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6, haloalqueniloxi C2-6, cianoalcoxi C1-6, alcoxi C1-6-alcoxi C1-6, alcoxi C1-6-alcoxi C1-6-alcoxi C1-6, alquiltio C1-6-alcoxi C1-6, alquilsulfinil C1-6-alcoxi C1-6, alquilsulfonil C1-6-alcoxi C1-6, alcoxi C1-6-carbonil-alcoxi C1-6, formiloxi, alquilcarboniloxi C1-6, alquilcarbonilo C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquiltio C1-6, haloalquilsulfinilo C1-6 o haloalquilsulfonilo C1-6, alquiltiocarbonilo C1-6, alquilamino C1-6, di(alquil C1-6)amino, alquilsulfoniloxi C1-4, alquilcarbonilamino C1-4, N(alquil C1-4)- alquilcarbonilamino C1-4, alcoxicarbonilamino C1-4, N(alquil C1-4)-alcoxicarbonilamino C1-4, alquilsulfonilamino C1-4, N(alquil C1-4)-alquilsulfonilamino C1-4, OSO2-alquilo C1-4, rodano, tri-alquil C1-4sililo, alquil C1-4-alcoxi C1-4fosfino o dialcoxi C1-4fosfono; o X6 es un sistema anular mono- o bicíclico de 3 a 10 miembros, que puede ser aromático, saturado o parcialmente saturado y puede contener de 1 a 4 heteroátomos seleccionados del grupo que consta de nitrogeno, oxígeno, azufre, - S(O)-, -S(O)2-, -N(Ra26)-, -C(O)- y C(=NORa7), y cada sistema anular puede contener no más de dos átomos de oxígeno y no más de dos átomos de azufre, y el sistema anular en sí mismo puede estar mono- o polisustituido con alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, hidroxi, alcoxi C1-6, haloalcoxi C1-6, alqueniloxi C3-6, alquiniloxi C3-6, mercapto, alquiltio C1-6, haloalquiltio C1-6, alqueniltio C3-6, haloalqueniltio C3-6, alquiniltio C3-6, alcoxialquiltio C2-5, acetilalquiltio C3-5, alcoxicarbonilalquiltio C3-6, cianoalquiltio C2-4, alquilsulfinilo C1-6, haloalquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, aminosulfonilo, alquilaminosulfonilo C1- 4, di(alquil C1-4)aminosulfonilo, amino, alquilamino C1-4, di(alquil C1-4)amino, halogeno, ciano, nitro, fenilo, fenoxi, feniltio, benciloxi y/o con benciltio, siendo posible que los grupos fenilo a su vez estén sustituidos en el anillo fenilo con alquilo C1-3, haloalquilo C1-3, alcoxi C1-3, haloalcoxi C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, aminosulfonilo, alquilaminosulfonilo C1-2, di(alquil C1-2)aminosulfonilo, di(alquil C1-4)amino, alcoxicarbonilo C1-4, halogeno, ciano o nitro; R3 es hidrogeno, alquilo C1-4, haloalquilo C1-4, alcoxi C1-2-alquilo C1-2 o fenilo, que a su vez puede estar mono- o polisustituido con alquilo C1-3, haloalquilo C1-3, alcoxi C1-3, haloalcoxi C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1- 3, aminosulfonilo, alquilaminosulfonilo C1-2, di(alquil C1-2)aminosulfonilo, di(alquil C1-4)amino, alcoxicarbonilo C1-4, halogeno, ciano o nitro; Ra21 es hidrogeno, alquilo C1-4 o alcoxi C1-2-alquilo C1-2; Ra22 es hidrogeno, alquilo C1-4 o fenilo, que puede estar mono- o polisustituido con alquilo C1-3, haloalquilo C1-3, alcoxi C1-3, haloalcoxi C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, aminosulfonilo, alquilaminosulfonilo C1-2, di(alquil C1-2)aminosulfonilo, di(alquil C1-4)amino, alcoxicarbonilo C1-4, halogeno, ciano o nitro; Ra23 es hidrogeno, formilo, alquilo C1-4, alquilcarbonilo C1-4, haloalquilcarbonilo C1-4 o alcoxicarbonilo C1-4; Ra25 es alquilo C1-4, o es bencilo que puede estar mono- o polisustituido con alquilo C1- 3, haloalquilo C1-3, alcoxi C1-3, haloalcoxi C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, aminosulfonilo, alquilaminosulfonilo C1-2, di(alquil C1-2)aminosulfonilo, di(alquil C1-4)amino, alcoxicarbonilo C1-4, halogeno, ciano o nitro; Ra24 y Ra26 independientemente entre sí, son hidrogeno, alquilo C1-4, alquiltiocarbonilo C1-4, alcoxicarbonilo C1-4, alquilcarbonilo C1-4, cicloalquilcarbonilo C3-4, fenilcarbonilo o fenilo, siendo posible que los grupos fenilo a su vez estén mono- o polisustituidos con alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, alquilcarbonilo C1-4, alcoxicarbonilo C1-4, alquilamino C1-4, di-alquilamino C1-4, alquil C1-4-S, alquil C1-4-S(O), alquil C1-4-SO2, alquil C1-4-S(O)2O, haloalquil C1- 4-S, haloalquil C1-4-S(O), haloalquil C1-4-SO2, haloalquil C1-4-S(O)2O, alquil C1-4-S(O)2NH, alquil C1-4-S(O)2N(alquil C1-4), halogeno, nitro o con ciano; R4 es hidrogeno, hidroxi, halogeno, ciano, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquiltio C1-6, haloalquilsulfinilo C1-6, haloalquilsulfonilo C1-6, alquilcarbonilsulfonilo C1-6, di-alquilaminosulfonilo C2-6, alquilsulfoniloxi C1-6, amino, alquilsulfonilamino C1-4, N(alquil C1-4)-alquilsulfonilamino C1-4, nitro, triazolilo, furilo o fenilo, siendo posible que el fenilo a su vez esté mono- o polisustituido con alquilo C1-3, haloalquilo C1-3, alcoxi C1-3, haloalcoxi C1-3, alquilsulfonilo C1-3, haloalquilsulfonilo C1-3, aminosulfonilo, alquilaminosulfonilo C1-2, di(alquil C1-2)aminosulfonilo, di(alquil C1-4)amino, alcoxicarbonilo C1-4, halogeno, ciano o nitro, R5 es H, halogeno, alquilo C1-3, haloalquilo C1-3 o alcoxi C1-3; Q es un grupo de formula (2) donde A1 es C(R11R12) o NR13; A2 es C(R14R15)m, C(O), O, NR16 o S(O)q; A3 es C(R17R18) o NR19 con la salvedad que A2 es diferente de S(O)q cuando A1 es NR13 y/o A3 es NR19; R6 es hidroxi, O-M+, donde M+ es un cation metálico o un cation amonio; halogeno o S(O)nR9, donde m es 1 o 2; q, n y k son cada uno, independientemente de los demás, 0, 1 o 2; R9 es alquilo C1-12, alquenilo C2-12, alquinilo C2-12, alenilo C3-12, cicloalquilo C3-12, cicloalquenilo C5-12, R10-alquileno C1-12 o R10-alquenileno C1-12, donde alquileno o alquenileno pueden estar interrumpidos con -O-, -S(O)k y/o -C(O)- y pueden estar mono- o polisustituidos con hidroxi, halogeno, alquilo C1-6, alcoxi C1-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, ciano, carbamoilo, carboxi, alcoxicarbonilo C1-4 o fenilo; siendo posible que el fenilo esté sustituido con halogeno, alquilo C1-3, haloalquilo C1-3, hidroxi, alcoxi C1- 3, haloalcoxi C1-3, ciano o nitro; o R9 es fenilo o heteroarilo, donde cada uno puede estar mono-, di- o trisustituido con halogeno, alquilo C1-3, haloalquilo C1-3, hidroxi, alcoxi C1-3, haloalcoxi C1-3, ciano o nitro; R10 es halogeno, ciano, rodano, hidroxi, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, alqueniltio C2-6, alquiniltio C2-6, alquilsulfoniloxi C1-6, fenilsulfoniloxi, alquilcarboniloxi C1-6, benzoiloxi, alcoxicarboniloxi C1-4, alquilcarbonilo C1-6, alcoxicarbonilo C1-4, benzoílo, aminocarbonilo, alquilaminocarbonilo C1-4, cicloalquilo C3-6, fenilo, fenoxi, feniltio, fenilsulfinilo o fenilsulfonilo; siendo posible que los grupos que contienen fenilo a su vez estén mono- o polisustituidos con halogeno, alquilo C1-3, haloalquilo C1-3, hidroxi, alcoxi C1-3, haloalcoxi C1-3, ciano o nitro; R11 y R17 son cada uno independientemente del otro hidrogeno, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, alcoxicarbonilo C1-4, hidroxi, alcoxi C1-4, alqueniloxi C3-4, alquiniloxi C3-4, hidroxi-
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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EP06014495 | 2006-07-12 |
Publications (1)
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AR061888A1 true AR061888A1 (es) | 2008-10-01 |
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ARP070103084A AR061888A1 (es) | 2006-07-12 | 2007-07-11 | Herbicidas derivados de (1,2,4)-triazolo-(4,3-a)piridina |
Country Status (6)
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US (1) | US20100035756A1 (es) |
EP (1) | EP2046788A1 (es) |
AR (1) | AR061888A1 (es) |
AU (1) | AU2007272009A1 (es) |
CA (1) | CA2656855A1 (es) |
WO (1) | WO2008006540A1 (es) |
Families Citing this family (61)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
AR059898A1 (es) | 2006-03-15 | 2008-05-07 | Janssen Pharmaceutica Nv | Derivados de 3-ciano-piridona 1,4-disustituida y su uso como moduladores alostericos de los receptores mglur2 |
AU2007291190A1 (en) * | 2006-08-30 | 2008-03-06 | Cellzome Limited | Triazole derivatives as kinase inhibitors |
TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
AU2008297876B2 (en) | 2007-09-14 | 2011-07-07 | Addex Pharma S.A. | 1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones |
BRPI0816767B8 (pt) | 2007-09-14 | 2021-05-25 | Addex Pharmaceuticals Sa | composto 4-fenil-3,4,5,6-tetra-hidro-2h,1'h-[1,4']bipiridi¬nil-2'-onas 1',3'-dissubstituídas, composição farmacêutica e uso dos mesmos |
CN101801930B (zh) | 2007-09-14 | 2013-01-30 | 奥梅-杨森制药有限公司 | 1,3-二取代的-4-苯基-1h-吡啶-2-酮 |
ES2637794T3 (es) | 2007-11-14 | 2017-10-17 | Janssen Pharmaceuticals, Inc. | Derivados de imidazo[1,2-A]piridina y su uso como moduladores alostéricos positivos de receptores MGLUR2 |
BRPI0819606A2 (pt) | 2007-11-27 | 2017-05-09 | Cellzome Ltd | amino triazóis como inobidores de pi3k |
WO2009126624A1 (en) | 2008-04-11 | 2009-10-15 | Bristol-Myers Squibb Company | Triazolo compounds useful as dgat1 inhibitors |
WO2009126861A2 (en) | 2008-04-11 | 2009-10-15 | Bristol-Myers Squibb Company | Triazolopyridine compounds useful as dgat1 inhibitors |
AU2009289784B2 (en) | 2008-09-02 | 2012-03-22 | Addex Pharma S.A. | 3-azabicyclo[3.1.0]hexyl derivatives as modulators of metabotropic glutamate receptors |
WO2010043396A1 (en) | 2008-10-16 | 2010-04-22 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
WO2010060589A1 (en) | 2008-11-28 | 2010-06-03 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors |
SI2379548T1 (sl) * | 2008-12-19 | 2016-06-30 | Leo Pharma A/S | Triazolopiridini kot fosfodiesterazni inhibitorji za zdravljenje kožnih bolezni |
US8946205B2 (en) | 2009-05-12 | 2015-02-03 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
MY161325A (en) * | 2009-05-12 | 2017-04-14 | Janssen Pharmaceuticals Inc | 1, 2, 4-triazolo[4,3-a]pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders |
MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
WO2010141796A2 (en) | 2009-06-05 | 2010-12-09 | Cephalon, Inc. | PREPARATION AND USES OF 1,2,4-TRIAZOLO [1,5a] PYRIDINE DERIVATIVES |
SI2448938T1 (sl) | 2009-06-29 | 2014-08-29 | Incyte Corporation Experimental Station | Pirimidinoni kot zaviralci pi3k |
PE20120629A1 (es) | 2009-07-17 | 2012-05-30 | Japan Tobacco Inc | Compuesto triazolopiridina y su accion como inhibidor de prolil hidroxilasa e inductor de la produccion de eritropoyetina |
AU2010276537B2 (en) * | 2009-07-27 | 2015-04-16 | Gilead Sciences, Inc. | Fused heterocyclic compounds as ion channel modulators |
EP2343294A1 (en) | 2009-11-30 | 2011-07-13 | Bayer Schering Pharma AG | Substituted triazolopyridines |
AR079529A1 (es) * | 2009-12-18 | 2012-02-01 | Incyte Corp | Derivados arilo y heteroarilo sustituidos y fundidos como inhibidores de la pi3k |
WO2011075643A1 (en) | 2009-12-18 | 2011-06-23 | Incyte Corporation | Substituted heteroaryl fused derivatives as pi3k inhibitors |
US9193721B2 (en) | 2010-04-14 | 2015-11-24 | Incyte Holdings Corporation | Fused derivatives as PI3Kδ inhibitors |
WO2011163195A1 (en) | 2010-06-21 | 2011-12-29 | Incyte Corporation | Fused pyrrole derivatives as pi3k inhibitors |
MX2012015096A (es) | 2010-07-02 | 2013-05-28 | Gilead Sciences Inc | Compuestos heterociclicos fusionados como moduladores del canal ion. |
US8981116B2 (en) | 2010-07-23 | 2015-03-17 | Solvay Sa | Process for the preparation of esters of 1-substituted-3-fluoroalkyl-pyrazole-4-carboxylic acids |
CN103261195B (zh) | 2010-11-08 | 2015-09-02 | 杨森制药公司 | 1,2,4-三唑并[4,3-a]吡啶衍生物及其作为MGLUR2受体的正变构调节剂的用途 |
AU2011328203B2 (en) | 2010-11-08 | 2015-03-19 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
PL2649069T3 (pl) * | 2010-11-08 | 2016-01-29 | Janssen Pharmaceuticals Inc | Pochodne 1,2,4-triazolo[4,3-a]pirydyny i ich zastosowanie jako dodatnich allosterycznych modulatorów receptorów mGluR2 |
WO2012065297A1 (en) * | 2010-11-16 | 2012-05-24 | Impact Therapeutics, Inc. | 3-ARYL-6-ARYL-[1,2,4]TRIAZOLO[4,3-a]PYRIDINES AS INHIBITORS OF CELL PROLIFERATION AND THE USE THEREOF |
CN103370316B (zh) * | 2010-11-16 | 2015-06-24 | 南京英派药业有限公司 | 作为细胞增殖抑制剂的3-芳基-6-芳基-[1,2,4]三唑并[4,3-a]吡啶及其应用 |
JP5961187B2 (ja) | 2010-12-20 | 2016-08-02 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Pi3k阻害剤としてのn−(1−(置換フェニル)エチル)−9h−プリン−6−アミン |
US9108984B2 (en) | 2011-03-14 | 2015-08-18 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors |
WO2012135009A1 (en) | 2011-03-25 | 2012-10-04 | Incyte Corporation | Pyrimidine-4,6-diamine derivatives as pi3k inhibitors |
EP2707361B1 (en) | 2011-05-10 | 2017-08-23 | Gilead Sciences, Inc. | Fused heterocyclic compounds as sodium channel modulators |
NO3175985T3 (es) | 2011-07-01 | 2018-04-28 | ||
TWI622583B (zh) | 2011-07-01 | 2018-05-01 | 基利科學股份有限公司 | 作為離子通道調節劑之稠合雜環化合物 |
CA2846652C (en) | 2011-09-02 | 2019-11-05 | Incyte Corporation | Heterocyclylamines as pi3k inhibitors |
EP2757882B1 (en) | 2011-09-22 | 2020-11-04 | Merck Sharp & Dohme Corp. | Imidazopyridyl compounds as aldosterone synthase inhibitors |
EP2757883B1 (en) * | 2011-09-22 | 2021-01-13 | Merck Sharp & Dohme Corp. | Triazolopyridyl compounds as aldosterone synthase inhibitors |
AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
AU2014271662B2 (en) | 2013-05-31 | 2018-03-01 | Nissan Chemical Corporation | Heterocyclic amide compound |
JO3368B1 (ar) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2 |
JO3367B1 (ar) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2 |
TWI652014B (zh) | 2013-09-13 | 2019-03-01 | 美商艾佛艾姆希公司 | 雜環取代之雙環唑殺蟲劑 |
UA121965C2 (uk) | 2014-01-21 | 2020-08-25 | Янссен Фармацевтика Нв | Комбінації, які містять позитивні алостеричні модулятори або ортостеричні агоністи метаботропного глутаматергічного рецептора 2 підтипу, та їх застосування |
KR102461134B1 (ko) | 2014-01-21 | 2022-10-28 | 얀센 파마슈티카 엔.브이. | 대사 조절형 글루탐산 작동성 수용체 제2아형의 양성 알로스테릭 조절제 또는 오르토스테릭 작동제를 포함하는 조합 및 그 용도 |
JP6462703B2 (ja) * | 2014-01-24 | 2019-01-30 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 1−アルキル−3−ジフルオロメチル−5−フルオロ−1h−ピラゾール−4−カルバルデヒド類及び1−アルキル−3−ジフルオロメチル−5−フルオロ−1h−ピラゾール−4−カルボキシレート類を調製する方法 |
WO2015191677A1 (en) | 2014-06-11 | 2015-12-17 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors |
ES2843522T3 (es) | 2015-02-27 | 2021-07-19 | Incyte Corp | Sales del inhibidor de PI3K y procesos para su preparación |
CN107635984B (zh) | 2015-03-11 | 2021-04-13 | Fmc公司 | 杂环取代的二环唑杀有害生物剂 |
BR112017019326B1 (pt) | 2015-03-12 | 2022-04-26 | Fmc Corporation | Composto, composição e método para controlar uma praga invertebrada |
WO2016183060A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
WO2016183063A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Crystalline forms of a pi3k inhibitor |
EP3359545B1 (en) | 2015-10-08 | 2024-03-20 | FMC Corporation | Heterocycle-substituted bicyclic azole pesticides |
WO2021008607A1 (zh) * | 2019-07-18 | 2021-01-21 | 青岛清原化合物有限公司 | 取代的1,2,4-三唑并[4,3-a]吡啶衍生物及其制备方法、除草组合物和应用 |
WO2021152055A1 (en) * | 2020-01-31 | 2021-08-05 | Solvay Sa | Process for the manufacture of haloalkyl substituted pyridine compounds |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1670140A1 (de) * | 1966-08-31 | 1970-10-29 | Boehringer Mannheim Gmbh | Verfahren zur Herstellung von 3-[2-(5-Nitrofuryl-2)-vinyl]-s-triazolo[4,3-a]pyridin-Derivaten |
DE1670139A1 (de) * | 1966-08-31 | 1970-10-29 | Boehringer Mannheim Gmbh | Verfahren zur Herstellung von 3-(5-Nitrofuryl-2)-s-triazolo[4.3-a]pyridin-Derivaten |
DE2025427A1 (en) * | 1970-05-25 | 1971-12-09 | Badische Anilin- & Soda-Fabrik Ag, 6700 Ludwigshafen | 2,6-dihydroxy-3-oxo-pyridine cpds prodn- from 2,6-dihydroxy cpds, - starting materials for dyes and pesticides |
US4650872A (en) * | 1985-08-01 | 1987-03-17 | Merrell Dow Pharmaceuticals Inc. | 5-chloro-s-triazolo[4,3-a]-pyridine-7-carboxylic acids, useful as antiallergic agents |
CA1340284C (en) * | 1987-03-19 | 1998-12-22 | Zeneca Inc. | Herbicidal substituted cyclic diones |
DE4007025A1 (de) * | 1990-03-02 | 1991-09-05 | Schering Ag | Mittel mit herbizider wirkung mit einem gehalt an in 3-stellung aliphatisch substituierten 1,2,4-triazolo (4,3-a)pyridinen |
IL96432A0 (en) * | 1989-11-30 | 1991-08-16 | Schering Ag | Pesticidal compositions containing pyridine derivatives and novel pyridine derivatives |
EP0684823A4 (en) * | 1993-02-22 | 1997-07-09 | Merck & Co Inc | FIBRINOGEN RECEPTOR ANTAGONISTS. |
US5332718A (en) * | 1993-03-15 | 1994-07-26 | E. I. Du Pont De Nemours And Company | Herbicidal substituted bicyclic triazoles for plantation crops |
US5571775A (en) * | 1994-07-11 | 1996-11-05 | Dowelanco | N-aryl[1,2,4]triazolo[1,5-a]pyridine-2-sulfonamide herbicides |
EP0922032A1 (en) * | 1996-06-06 | 1999-06-16 | E.I. Du Pont De Nemours And Company | Herbicidal pyridinyl and pyrazolylphenyl ketones |
ATE296803T1 (de) * | 1998-09-15 | 2005-06-15 | Syngenta Participations Ag | Als herbicide verwendbare pyridin-ketone |
JP2002544201A (ja) * | 1999-05-07 | 2002-12-24 | ビーエーエスエフ アクチェンゲゼルシャフト | ベンゾヘテロシクリルシクロヘキセノン |
US6506772B1 (en) * | 2000-12-15 | 2003-01-14 | Hoffmann-La Roche Inc. | Substituted [1,2,4]triazolo[1,5a]pyridine derivatives with activity as adenosine receptor ligands |
MY139563A (en) * | 2002-09-04 | 2009-10-30 | Bristol Myers Squibb Co | Heterocyclic aromatic compounds useful as growth hormone secretagogues |
CA2582482A1 (en) * | 2004-10-07 | 2006-04-13 | Warner-Lambert Company Llc | Triazolopyridine derivatives as antibacterial agents |
EP1971594A2 (en) * | 2005-11-21 | 2008-09-24 | Biogen Idec MA Inc. | Substituted pyrazalones |
-
2007
- 2007-07-10 US US12/373,309 patent/US20100035756A1/en not_active Abandoned
- 2007-07-10 EP EP07785956A patent/EP2046788A1/en not_active Withdrawn
- 2007-07-10 AU AU2007272009A patent/AU2007272009A1/en not_active Abandoned
- 2007-07-10 CA CA002656855A patent/CA2656855A1/en not_active Abandoned
- 2007-07-10 WO PCT/EP2007/006086 patent/WO2008006540A1/en active Application Filing
- 2007-07-11 AR ARP070103084A patent/AR061888A1/es not_active Application Discontinuation
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EP2046788A1 (en) | 2009-04-15 |
AU2007272009A1 (en) | 2008-01-17 |
WO2008006540A1 (en) | 2008-01-17 |
US20100035756A1 (en) | 2010-02-11 |
CA2656855A1 (en) | 2008-01-17 |
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