AR073560A1 - Compuestos de triazol y su uso como antimicotico - Google Patents
Compuestos de triazol y su uso como antimicoticoInfo
- Publication number
- AR073560A1 AR073560A1 ARP090103454A ARP090103454A AR073560A1 AR 073560 A1 AR073560 A1 AR 073560A1 AR P090103454 A ARP090103454 A AR P090103454A AR P090103454 A ARP090103454 A AR P090103454A AR 073560 A1 AR073560 A1 AR 073560A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkynyl
- alkenyl
- phenyl
- oxy
- Prior art date
Links
- QWENRTYMTSOGBR-UHFFFAOYSA-N 1H-1,2,3-Triazole Chemical class C=1C=NNN=1 QWENRTYMTSOGBR-UHFFFAOYSA-N 0.000 title 1
- 230000000416 anti-micotic effect Effects 0.000 title 1
- -1 phenoxy, phenyl Chemical group 0.000 abstract 20
- 125000000217 alkyl group Chemical group 0.000 abstract 15
- 125000000304 alkynyl group Chemical group 0.000 abstract 10
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 9
- 125000001188 haloalkyl group Chemical group 0.000 abstract 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 9
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 6
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 5
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 5
- 125000006717 (C3-C10) cycloalkenyl group Chemical group 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 abstract 2
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 abstract 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 abstract 2
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 2
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 abstract 1
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 abstract 1
- 125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 125000001931 aliphatic 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
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 1
- 125000005529 alkyleneoxy 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
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 1
- 125000005844 heterocyclyloxy group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- ZSOVXEHFNLKBCP-UHFFFAOYSA-N nitro peroxycyanate Chemical compound C(#N)OO[N+](=O)[O-] ZSOVXEHFNLKBCP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 abstract 1
- 125000005702 oxyalkylene group Chemical group 0.000 abstract 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Pulmonology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Reivindicacion 1: Compuestos caracterizados porque tienen la formula 1 en donde las variables presentan los siguientes significados: R1 es alquilo C1-10, haloalquilo C1-10, alquenilo C2-10, halogenalquenilo C2-10, alquinilo C2-10, halogenalquinilo C3-10, cicloalquilo C3-8, halogencicloalquilo C3-8, cicloalquenilo C3-10, halogencicloalquenilo C3-10, en donde los grupos previamente mencionados no están sustituidos o pueden contener 1, 2, 3, 4 o 5 sustituyentes seleccionados de modo independiente de halogeno, hidroxi, alquilo C1-8, halogenalquilo C1-8, alquenilo C2-8, halogenalquenilo C2-8, alquinilo C2-8, halogenalquinilo C3-8 y fenilo, en donde el fenilo no está, a su vez, sustituido o está sustituido con 1, 2, 3, 4 o 5 sustituyentes L seleccionados de modo independiente; o arilo de 6 a 10 miembros, que no está sustituido o está sustituido con 1, 2, 3, 4 o 5 sustituyentes L seleccionados de modo independiente, en donde L es halogeno, ciano, nitro, hidroxi, cianato (OCN), alquilo C1-8, halogenalquilo C1-8, alquenilo C2-8, halogenalquenilo C2-8, alquinilo C2-8, halogenalquinilo C3-8, alcadienilo C4-10, halogenalcadienilo C4-10, alcoxi C1-8, halogenalcoxi C1-8, alquil C1-8-carboniloxi, alquil C1-8-sulfoniloxi, alquenil C2-8-oxi, halogenalquenil C2-8-oxi, alquinil C2-8-oxi, halogenalquinil C3-8-oxi, cicloalquilo C3-8, halogencicloalquilo C3-8, cicloalquenilo C3-8, halogencicloalquenilo C3-8, cicloalcoxi C3-8, cicloalquenil C3-6-oxi, hidroxiimino-alquilo C1-8, alquileno C1-6, oxi-alquileno C2-4, oxi-alquilen C1-3-oxi, alcoximino C1-8-alquilo C1-8, alquenil C2-8-oximino-alquilo C1-8, alquinil C2-8-oximino-alquilo C1-8, S(=O)nA1, C(=O)A2, C(=S)A2, NA3A4, fenoxi, fenilo, heteroariloxi, heterocicliloxi, heteroarilo, heterociclilo, en donde en los grupos previamente mencionados el heteroarilo es un heterociclo aromático de cinco, seis o siete miembros y el heterociclilo es un heterociclo saturado o parcialmente insaturado de cinco, seis o siete miembros, que contienen, en cada caso, uno, dos, tres o cuatro heteroátomos del grupo O, N y S; en donde n, A1, A2, A3, A4 son: n es 0, 1 o 2; A1 es hidrogeno, hidroxi, alquilo C1-8, halogenalquilo C1-8, amino, alquil C1-8-amino, di-alquil C1-8-amino, fenilo, fenilamino o fenil-alquil C1-8-amino; A2 es uno de los grupos mencionados en A1 o es alquenilo C2-8, halogenalquenilo C2-8, alquinilo C2-8, halogenalquinilo C3-8, alcoxi C1-8, halogenalcoxi C1-8, alquenil C2-8-oxi, halogenalquenil C2-8-oxi, alquinil C2-8-oxi, halogenalquinil C3-8-oxi, cicloalquilo C3-8, halogencicloalquilo C3-8, cicloalcoxi C3-8 o halogencicloalcoxi C3-8; A3, A4 son, de modo independiente entre si, hidrogeno, alquilo C1-8, halogenalquilo C1-8, alquenilo C2-8, halogenalquenilo C2-8, alquinilo C2-8, halogenalquinilo C3-8, cicloalquilo C3-8, halogencicloalquilo C3-8, cicloalquenilo C3-8 o halogencicloalquenilo C3-8, fenilo o heteroarilo de 5 o 6 miembros con uno, dos, tres o cuatro heteroátomos del grupo O, N y S en el heterociclo; los grupos alifáticos y/o alicíclicos y/o aromáticos de las definiciones de los radicales de L pueden llevar, a su vez, uno, dos, tres o cuatro grupos RL iguales o diferentes: RL es halogeno, hidroxi, ciano, nitro, alquilo C1-8, halogenalquilo C1-8, alcoxi C1-8, halogenalcoxi C1-8, cicloalquilo C3-8, halogencicloalquilo C3-8, cicloalquenilo C3-8, cicloalcoxi C3-8, halogencicloalcoxi C3-8, alquileno C1-6, oxi-alquileno C2-4, oxi-alquilen C1-3-oxi, alquil C1-8-carbonilo, alquil C1-8-carboniloxi, alcoxi C1-8-carbonilo, amino, alquil C1-8-amino, di-alquil C1-8-amino; R2 es hidrogeno, alquilo C1-10, halogenalquilo C1-10, alquenilo C2-10, halogenalquenilo C2-10, alquinilo C2-10, halogenalquinilo C3-10, alcadienilo C4-10, halogenalcadienilo C4-10, cicloalquilo C3-10, halogencicloalquilo C3-10, cicloalquenilo C3-10, halogencicloalquenilo C3-10; R3 es hidrogeno, alquilo C1-10, halogenalquilo C1-10, alquenilo C2-10, halogenalquenilo C2-10, alquinilo C2-10, halogenalquinilo C3-10, alcadienilo C4-10, halogenalcadienilo C4-10, cicloalquilo C3-10, halogencicloalquilo C3-10, cicloalquenilo C3-10, halogencicloalquenilo C3-10; carboxilo, formilo, Si(A5A6A7), C(O)R?, C(O)OR?, C(S)OR?, C(O)SR?, C(S)SR?, C(NRA)SR?, C(S)R?, C(NR?)N-NA3A4, C(NR?)RA, C(NR?)ORA, C(O)NA3A4, C(S)NA3A4 o S(=O)nA1; en donde R? es alquilo C1-8, alquenilo C3-8, alquinilo C3-8, cicloalquilo C3-6, cicloalquenilo C3-6 o fenilo; RA es alquilo C1-8, alquenilo C3-8, alquinilo C3-8, cicloalquilo C3-6, cicloalquenilo C3-6 o fenilo; A5, A6, A7 son, de modo independiente entre sí, alquilo C1-10, alquenilo C3-8, alquinilo C3-8, cicloalquilo C3-6, cicloalquenilo C3-6 o fenilo; en donde R?, RA, A5, A6 y A7, siempre que no se indique otra cosa, de modo independiente entre sí, no están sustituidos o están sustituidos con uno, dos, tres, cuatro o cinco L, tal corno se definio con anterioridad; R4 es hidrogeno, alquilo C1-10, halogenalquilo C1-10, alquenilo C2-10, halogenalquenilo C2-10, alquinilo C2-10, halogenalquinilo C3-10, alcadienilo C4-10, halogenalcadienilo C4-10, cicloalquilo C3-10, halogencicloalquilo C3-10, cicloalquenilo C3-10, halogencicloalquenilo C3-10; R2, R3 y R4 siempre que no se indique otra cosa, de modo independiente entre sí, no están sustituidos o están sustituidos con uno, dos, tres, cuatro o cinco L, tal como se definio con anterioridad; con la condicion de que R1 no sea fenilo no sustituido cuando R2 y R3 son H, y R1 no sea fenilo no sustituido cuando R2 y R4 son H, y R1 no es 4-fluorofenilo, 3-clorofenilo, 4-clorofenilo, 3-trifluoroetilfenilo o 2,4-diclorofenoilo cunado R2 y R3 H y R4 metilo, alquenilo C2-10 o alquinilo C2-10, y R1 no es 2-fluorofenilo, 4-fluorofenilo, 2-clorofenilo, 3-clorofenilo, 4-clorofenilo, 2-metoxifenilo, 3-metoxifenilo, 4-metoxifenilo, 3-metilfenilo, 3-n-butoxifenilo, 3-ter-butoxifenilo, 4-fenoxifenilo, 3-(2-fluorofenoxi)fenilo, 3-(3-clorofenoxi)fenilo, 2-metilfenilo, 3-metilfenilo, 4-metilfenilo, 2-n-propilfenilo, 3-iso-propilfenilo, 4-iso-propilfenilo, 3-ter-butilfenilo, 3-trifluoroetilfenilo, 4-trifluoroetilfenilo, 3-fenilfenilo, 3-(3-clorofenil)fenilo, 3-(4-clorofenil)fenilo, 2,4-diclorofenoilo, 2,6-diclorofenoilo, 3,5-diclorofenoilo o 2,4,6-triclorofenilo cuando R2, R3 y R4 son H; y sus sales de tolerancia en agricultura.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08163963 | 2008-09-09 | ||
| EP09155511 | 2009-03-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR073560A1 true AR073560A1 (es) | 2010-11-17 |
Family
ID=41171131
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090103454A AR073560A1 (es) | 2008-09-09 | 2009-09-09 | Compuestos de triazol y su uso como antimicotico |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20110160056A1 (es) |
| EP (1) | EP2328878A1 (es) |
| JP (1) | JP2012502001A (es) |
| CN (1) | CN102149691A (es) |
| AR (1) | AR073560A1 (es) |
| BR (1) | BRPI0919142A2 (es) |
| UY (1) | UY32102A (es) |
| WO (1) | WO2010029000A1 (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2513067A1 (en) | 2009-12-18 | 2012-10-24 | Basf Se | Method for producing triazolinthione derivatives and intermediates thereof |
| WO2011110583A2 (en) | 2010-03-10 | 2011-09-15 | Basf Se | Fungicidal mixtures comprising triazole derivatives |
| EA201201288A1 (ru) | 2010-03-16 | 2013-04-30 | Басф Се | Способ применения реактивов гриньяра |
| WO2012041858A1 (en) | 2010-09-30 | 2012-04-05 | Basf Se | A process for the synthesis of thio-triazolo-group containing compounds |
| WO2012130823A1 (en) | 2011-03-30 | 2012-10-04 | Basf Se | Suspension concentrates |
| US10058542B1 (en) | 2014-09-12 | 2018-08-28 | Thioredoxin Systems Ab | Composition comprising selenazol or thiazolone derivatives and silver and method of treatment therewith |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3019049A1 (de) * | 1980-05-19 | 1981-12-03 | Basf Ag, 6700 Ludwigshafen | Neue azolverbindungen |
| DE3126022A1 (de) * | 1981-07-02 | 1983-01-13 | Basf Ag, 6700 Ludwigshafen | Azolverbindungen, verfahren zu ihrer herstellung und diese enthaltende fungizide |
| DE3151440A1 (de) * | 1981-12-24 | 1983-07-07 | Bayer Ag, 5090 Leverkusen | Antimykotische mittel |
| DE3321023A1 (de) * | 1983-06-10 | 1984-12-13 | Basf Ag, 6700 Ludwigshafen | Triazolylalkohole, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| DE3416444A1 (de) * | 1984-05-04 | 1985-11-07 | Basf Ag, 6700 Ludwigshafen | Verfahren zur diastereoselektiven reduktion von (alpha)-triazolylketonen zu ss-triazolylcarbinolen |
| DE3437919A1 (de) * | 1984-10-17 | 1986-04-17 | Basf Ag, 6700 Ludwigshafen | Benzyloxyalkylazole und diese enthaltende fungizide |
| DE3601430A1 (de) * | 1986-01-20 | 1987-07-23 | Basf Ag | Halogenierte azolverbindungen und diese enthaltende fungizide |
| DE3606947A1 (de) * | 1986-03-04 | 1987-09-10 | Basf Ag | Verfahren zur herstellung von phenoxyalkanoltriazolverbindungen und zwischenprodukte hierfuer |
| DE3724645A1 (de) * | 1987-07-25 | 1989-02-02 | Basf Ag | Hydroxyethyl-azol-derivate und ihre verwendung als fungizide |
-
2009
- 2009-09-03 CN CN200980135032XA patent/CN102149691A/zh active Pending
- 2009-09-03 EP EP09782532A patent/EP2328878A1/de not_active Withdrawn
- 2009-09-03 BR BRPI0919142A patent/BRPI0919142A2/pt not_active Application Discontinuation
- 2009-09-03 JP JP2011525543A patent/JP2012502001A/ja not_active Withdrawn
- 2009-09-03 US US13/062,524 patent/US20110160056A1/en not_active Abandoned
- 2009-09-03 WO PCT/EP2009/061368 patent/WO2010029000A1/de active Application Filing
- 2009-09-09 UY UY0001032102A patent/UY32102A/es unknown
- 2009-09-09 AR ARP090103454A patent/AR073560A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2328878A1 (de) | 2011-06-08 |
| JP2012502001A (ja) | 2012-01-26 |
| BRPI0919142A2 (pt) | 2015-12-08 |
| UY32102A (es) | 2010-03-26 |
| CN102149691A (zh) | 2011-08-10 |
| US20110160056A1 (en) | 2011-06-30 |
| WO2010029000A1 (de) | 2010-03-18 |
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