AR073476A1 - Anilinopirimidinas alcoxi y alquiltio sustituidas - Google Patents
Anilinopirimidinas alcoxi y alquiltio sustituidasInfo
- Publication number
- AR073476A1 AR073476A1 ARP090103356A ARP090103356A AR073476A1 AR 073476 A1 AR073476 A1 AR 073476A1 AR P090103356 A ARP090103356 A AR P090103356A AR P090103356 A ARP090103356 A AR P090103356A AR 073476 A1 AR073476 A1 AR 073476A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- alkyl
- unsubstituted
- alkoxy
- haloalkyl
- Prior art date
Links
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 16
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 11
- 239000001257 hydrogen Substances 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 8
- -1 alkylthio anilinopyrimidines Chemical class 0.000 abstract 7
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 5
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 239000001301 oxygen Substances 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 239000011593 sulfur Substances 0.000 abstract 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 2
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
- 241000233866 Fungi Species 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 229910052731 fluorine Inorganic materials 0.000 abstract 2
- 239000011737 fluorine Substances 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 230000003032 phytopathogenic effect Effects 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 abstract 1
- 108010081348 HRT1 protein Hairy Proteins 0.000 abstract 1
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 238000003898 horticulture Methods 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 125000006217 methyl sulfide group Chemical group [H]C([H])([H])S* 0.000 abstract 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000006299 oxetan-3-yl group Chemical group [H]C1([H])OC([H])([H])C1([H])* 0.000 abstract 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000005415 substituted alkoxy group Chemical group 0.000 abstract 1
- ZBZJXHCVGLJWFG-UHFFFAOYSA-N trichloromethyl(.) Chemical compound Cl[C](Cl)Cl ZBZJXHCVGLJWFG-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Las sales agroquímicamente activas de los mismos, su uso y procedimientos y composiciones para controlar hongos perjudiciales fitopatogenos en y/o sobre plantas o en y/o sobre semillas, procedimientos para preparar tales composiciones y tratar semillas y su uso para controlar hongos perjudiciales fitopatogenos en agricultura, horticultura y silvicultura, en la proteccion de materiales y en el campo doméstico y de la higiene. La presente se refiere, además, a procedimientos para la preparacion de anilinopirimidinas alcoxi y alquiltio sustituidas de la formula (1). Reivindicacion 1: Compuestos de la formula (1), en la cual uno o más de los símbolos tienen uno de los significados siguientes: R1 a R5, independientemente unos de otros, son hidrogeno, alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, alcoxi C1-4-alquilo C1-4, alcoxi C1-4-alcoxi C1-4 o halogeno, donde, de modo preciso, uno de los radicales R2 o R3 representa un grupo de la formula E1, E2 o E3, en las cuales uno o más de los símbolos tienen uno de los significados siguientes: X es oxígeno, NR14, azufre, SO o SO2, Y es un enlace directo, oxígeno, NR14, azufre, SO o SO2, n es 0,1 o 2, R6 es hidrogeno, alquilo C1-2, alcoxi C1-4-alquilo C1-4, trialquilsililo C1-4, trialquilsililetilo C1-4, dialquilmonofenilsililo C1-4, formilo, (alquilo C1-4)carbonilo, (alcoxi C1-4-alquilo C1-4)carbonilo, (alqueniloxi C3- 6)carbonilo, (cicloalquilo C3-6)carbonilo, (haloalcoxi C1-4-alquilo C1-4)carbonilo, (haloalquilo C1-4)carbonilo, (alcoxi C1-4)carbonilo, (haloalcoxi C1-4)carbonilo, benciloxicarbonilo, bencilo sustituido o no sustituido, alquenilo C2-6 sustituido o no sustituido, alquinilo C2-6 sustituido o no sustituido, alquilsulfinilo C1-2 o alquilsulfonilo C1-2, donde los sustituyentes, independientemente unos de otros, se seleccionan de entre hidrogeno, fluor, cloro o bromo, alquilo C1-4, alcoxi C1-4, hidroxilo, haloalquilo C1-4 o ciano, R7 es hidrogeno, alquilo C1-3, ciano o haloalquilo C1-3, R8 es metilo, fluor, cloro, bromo, SMe, SOMe, SO2Me, yodo, CCl3, CH2F, CHF2 o CF3, R9 es hidrogeno, alquilo C1-3 de cadena lineal o ramificado, 2-metoxietan-1-ilo, prop-2-en-1-ilo, alcoxi C1-4-alquilo C1-4, (alquil C1-4)carbonilo de cadena lineal o ramificado, (haloalquil C1-4)carbonilo, bencilo sustituido o no sustituido, trialquilsililo C1-6, trialquilsililetilo C1-4, dialquilmonofenilsililo C1-4, (alcoxi C1-4)carbonilo, alquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfinilo C1-6 o haloalquilsulfonilo C1-6, donde los sustituyentes, independientemente unos de otros, se seleccionan de entre hidrogeno, halogeno, nitro, alquilo C1-4, alcoxi C1-4, hidroxilo, haloalquilo C1-4 o ciano, R10 es alquilo C1-7 de cadena lineal o ramificado, sustituido o no sustituido, haloalquilo C2-7 de cadena lineal o ramificado, sustituido o no sustituido, cicloalquilo C3-7 sustituido o no sustituido, cicloalquilo C3-7-alquilo C1-3 de cadena lineal o ramificado, sustituido o no sustituido, alquenilo C3-7 de cadena lineal o ramificado, sustituido o no sustituido, alquinilo C3-7 de cadena lineal o ramificado, sustituido o no sustituido, alcoxi C1-4-alquilo C1-4 de cadena lineal o ramificado, sustituido o no sustituido, haloalcoxi C1-4-alquilo C1-4 de cadena lineal o ramificado, sustituido o no sustituido, 2-metil-1-(metilsulfanil)propan-2-ilo u oxetan-3-ilo, o R9 y R10 conjuntamente con el átomo de nitrogeno al que están unidos forman un ciclo saturado de 3 a 7 miembros, sustituido o no sustituido, que puede contener hasta un heteroátomo adicional seleccionado de entre oxígeno, azufre o nitrogeno, donde los sustituyentes de R10, independientemente unos de otros, se seleccionan de entre metilo, etilo, isopropilo, ciclopropilo, átomos de fluor, átomos de cloro y/o átomos de bromo, metoxi, etoxi, metilmercapto, etilmercapto, ciano, hidroxilo, CF3; R11 y R12. independientemente uno de otro, son hidrogeno, halogeno, alquilo C1-6, cicloalquilo C3-6 sustituido o no sustituido, cicloalquilo C3-6-alquilo C1-4 sustituido o no sustituido, haloalquilo C1-3, alcoxi C1-4-alquilo C1-4, alquenilo C2-4 sustituido o no sustituido, alquinilo C2-4 sustituido o no sustituido, fenilo sustituido o no sustituido o bencilo sustituido o no sustituido, donde los sustituyentes, independientemente unos de otros, se seleccionan de entre halogeno, alquilo C1-4 o haloalquilo C1-4, o R11 y R12 conjuntamente forman un grupo metileno = CH2; R13 es hidrogeno, alquilo C1-6, cicloalquilo C3-6 sustituido o no sustituido, cicloalquilo C3-6-alquilo C1-4 sustituido o no sustituido, haloalquilo C1-3, alcoxi C1-4-alquilo C1-4, alquenilo C2-4 sustituido o no sustituido, alquinilo C2-4 sustituido o no sustituido, fenilo sustituido o no sustituido o bencilo sustituido o no sustituido, donde los sustituyentes, independientemente unos de otros, se seleccionan de entre halogeno, alquilo C1-4 o haloalquilo C1-4, R14 es H, alquilo C1-6, alcoxi C1-4-alquilo C1-4 o bencilo sustituido o no sustituido, donde los sustituyentes, independientemente unos de otros, se seleccionan de entre halogeno, alquilo C1-4 o haloalquilo C1-4, y sales agroquímicamente activas de los mismos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08163607 | 2008-09-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR073476A1 true AR073476A1 (es) | 2010-11-10 |
Family
ID=41172469
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090103356A AR073476A1 (es) | 2008-09-03 | 2009-09-01 | Anilinopirimidinas alcoxi y alquiltio sustituidas |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20110245284A1 (es) |
| EP (1) | EP2331512A1 (es) |
| JP (1) | JP2012501980A (es) |
| KR (1) | KR20110049913A (es) |
| CN (1) | CN102203070A (es) |
| AR (1) | AR073476A1 (es) |
| BR (1) | BRPI0918078A2 (es) |
| EA (1) | EA201100439A1 (es) |
| TW (1) | TW201022211A (es) |
| WO (1) | WO2010025833A1 (es) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0914682B8 (pt) | 2008-06-27 | 2021-05-25 | Avila Therapeutics Inc | compostos de heteroarila e composições compreendendo os referidos compostos |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| US11351168B1 (en) | 2008-06-27 | 2022-06-07 | Celgene Car Llc | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| US9908884B2 (en) | 2009-05-05 | 2018-03-06 | Dana-Farber Cancer Institute, Inc. | EGFR inhibitors and methods of treating disorders |
| NZ607845A (en) | 2010-08-10 | 2015-03-27 | Celgene Avilomics Res Inc | Besylate salt of a btk inhibitor |
| US9238629B2 (en) | 2010-11-01 | 2016-01-19 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| CN103269704B (zh) | 2010-11-01 | 2018-07-06 | 西建卡尔有限责任公司 | 杂环化合物和其用途 |
| EP2637502B1 (en) | 2010-11-10 | 2018-01-10 | Celgene CAR LLC | Mutant-selective egfr inhibitors and uses thereof |
| TW201325593A (zh) | 2011-10-28 | 2013-07-01 | Celgene Avilomics Res Inc | 治療布魯頓（ｂｒｕｔｏｎ’ｓ）酪胺酸激酶疾病或病症之方法 |
| CN108658873B (zh) | 2012-03-15 | 2021-09-14 | 西建卡尔有限责任公司 | 表皮生长因子受体激酶抑制剂的固体形式 |
| JP6317320B2 (ja) | 2012-03-15 | 2018-04-25 | セルジーン シーエーアール エルエルシー | 上皮成長因子受容体キナーゼ阻害剤の塩 |
| EP2935226A4 (en) | 2012-12-21 | 2016-11-02 | Celgene Avilomics Res Inc | HETEROARYL COMPOUNDS AND USES THEREOF |
| CA2900012A1 (en) | 2013-02-08 | 2014-08-14 | Celgene Avilomics Research, Inc. | Erk inhibitors and uses thereof |
| US9492471B2 (en) | 2013-08-27 | 2016-11-15 | Celgene Avilomics Research, Inc. | Methods of treating a disease or disorder associated with Bruton'S Tyrosine Kinase |
| US9415049B2 (en) | 2013-12-20 | 2016-08-16 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| MX2016007898A (es) | 2013-12-20 | 2016-10-07 | Signal Pharm Llc | Compuestos diaminopirimidilo sustituidos, las composiciones de estos y los metodos de tratamiento con estos. |
| DK3179858T3 (da) | 2014-08-13 | 2019-07-22 | Celgene Car Llc | Forme og sammensætninger af en ERK-inhibitor |
| US9922507B2 (en) * | 2015-04-28 | 2018-03-20 | Ncr Corporation | Self-learning suppression of secondary barcodes |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4029650A1 (de) * | 1990-09-19 | 1992-03-26 | Hoechst Ag | 2-anilino-pyrimidine, verfahren zu ihrer herstellung, sie enthaltene mittel und ihre verwendung als fungizide |
| RS20050363A (sr) * | 2002-11-28 | 2007-11-15 | Schering Aktiengesellschaft, | Chk-,Pdk- I Akt-INHIBITORNI PIRIMIDINI, NJIHOVA PROIZVODNJA I UPOTREBA KAO FARMACEUTSKIH SREDSTAVA |
| DE102005008310A1 (de) * | 2005-02-17 | 2006-08-24 | Schering Ag | Verwendung von CDKII Inhibitoren zur Fertilitätskontrolle |
| DE102007010801A1 (de) * | 2007-03-02 | 2008-09-04 | Bayer Cropscience Ag | Diaminopyrimidine als Fungizide |
| JP2010522186A (ja) * | 2007-03-20 | 2010-07-01 | スミスクライン ビーチャム コーポレーション | 化合物 |
-
2009
- 2009-08-21 BR BRPI0918078A patent/BRPI0918078A2/pt not_active Application Discontinuation
- 2009-08-21 EP EP09778017A patent/EP2331512A1/de not_active Withdrawn
- 2009-08-21 US US13/061,896 patent/US20110245284A1/en not_active Abandoned
- 2009-08-21 JP JP2011525437A patent/JP2012501980A/ja not_active Withdrawn
- 2009-08-21 KR KR1020117007610A patent/KR20110049913A/ko not_active Withdrawn
- 2009-08-21 WO PCT/EP2009/006057 patent/WO2010025833A1/de not_active Ceased
- 2009-08-21 CN CN2009801435474A patent/CN102203070A/zh active Pending
- 2009-08-21 EA EA201100439A patent/EA201100439A1/ru unknown
- 2009-09-01 AR ARP090103356A patent/AR073476A1/es unknown
- 2009-09-02 TW TW098129479A patent/TW201022211A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2012501980A (ja) | 2012-01-26 |
| WO2010025833A1 (de) | 2010-03-11 |
| BRPI0918078A2 (pt) | 2016-06-14 |
| US20110245284A1 (en) | 2011-10-06 |
| EP2331512A1 (de) | 2011-06-15 |
| CN102203070A (zh) | 2011-09-28 |
| KR20110049913A (ko) | 2011-05-12 |
| TW201022211A (en) | 2010-06-16 |
| EA201100439A1 (ru) | 2011-12-30 |
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