HRP20190919T1 - Derivati n1-acil- 5-fluoropirimidinona - Google Patents
Derivati n1-acil- 5-fluoropirimidinona Download PDFInfo
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- HRP20190919T1 HRP20190919T1 HRP20190919TT HRP20190919T HRP20190919T1 HR P20190919 T1 HRP20190919 T1 HR P20190919T1 HR P20190919T T HRP20190919T T HR P20190919TT HR P20190919 T HRP20190919 T HR P20190919T HR P20190919 T1 HRP20190919 T1 HR P20190919T1
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- Prior art keywords
- alkyl
- benzyl
- optionally substituted
- phenyl
- compound
- Prior art date
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 21
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 18
- 150000001875 compounds Chemical class 0.000 claims 11
- -1 halothio Chemical group 0.000 claims 11
- 150000003839 salts Chemical class 0.000 claims 11
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 9
- 125000004122 cyclic group Chemical group 0.000 claims 9
- 125000005842 heteroatom Chemical group 0.000 claims 9
- 229920006395 saturated elastomer Polymers 0.000 claims 9
- 241000196324 Embryophyta Species 0.000 claims 8
- 229910052799 carbon Inorganic materials 0.000 claims 8
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 230000003287 optical effect Effects 0.000 claims 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 3
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 3
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 235000010290 biphenyl Nutrition 0.000 claims 3
- 239000004305 biphenyl Substances 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000004663 dialkyl amino group Chemical group 0.000 claims 3
- 244000053095 fungal pathogen Species 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 125000005843 halogen group Chemical group 0.000 claims 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims 3
- 125000001624 naphthyl group Chemical group 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- 239000004094 surface-active agent Substances 0.000 claims 3
- 241000209140 Triticum Species 0.000 claims 2
- 235000021307 Triticum Nutrition 0.000 claims 2
- 241001360088 Zymoseptoria tritici Species 0.000 claims 2
- 239000002671 adjuvant Substances 0.000 claims 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 2
- 235000017060 Arachis glabrata Nutrition 0.000 claims 1
- 244000105624 Arachis hypogaea Species 0.000 claims 1
- 235000010777 Arachis hypogaea Nutrition 0.000 claims 1
- 235000018262 Arachis monticola Nutrition 0.000 claims 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims 1
- 241000530549 Cercospora beticola Species 0.000 claims 1
- 241000233866 Fungi Species 0.000 claims 1
- 240000008790 Musa x paradisiaca Species 0.000 claims 1
- 235000018290 Musa x paradisiaca Nutrition 0.000 claims 1
- 241001281801 Mycosphaerella arachidis Species 0.000 claims 1
- 241001329956 Nothopassalora personata Species 0.000 claims 1
- 241000087479 Pseudocercospora fijiensis Species 0.000 claims 1
- 206010039509 Scab Diseases 0.000 claims 1
- 235000021536 Sugar beet Nutrition 0.000 claims 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims 1
- 241000228452 Venturia inaequalis Species 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 239000007900 aqueous suspension Substances 0.000 claims 1
- 239000012876 carrier material Substances 0.000 claims 1
- 239000012141 concentrate Substances 0.000 claims 1
- 235000008504 concentrate Nutrition 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 239000000428 dust Substances 0.000 claims 1
- 230000001804 emulsifying effect Effects 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 235000014666 liquid concentrate Nutrition 0.000 claims 1
- 239000002480 mineral oil Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 229920000847 nonoxynol Polymers 0.000 claims 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical group CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims 1
- 235000020232 peanut Nutrition 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000002689 soil Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 239000004546 suspension concentrate Substances 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 235000015112 vegetable and seed oil Nutrition 0.000 claims 1
- 239000008158 vegetable oil Substances 0.000 claims 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
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Claims (15)
1. Spoj s formulom II:
naznačen time što R1 je:
H;
C1-C6 alkil;
benzil; ili
-C(=O)R8;
R2 je:
H; ili
C1-C6 alkil;
alternativno R1 i R2 se mogu uzeti zajedno tako da tvore =CR11N(R12)R13;
R3 je:
-C(=O)R8; ili
-C(=S)R8;
R5 je neovisno halogen, C1-C6 alkil, C1-C6 haloalkil, C1-C6 alkoksi, C1-C6 haloalkoksi, C1-C6 alkiltio, C1-C6 haloalkiltio, halotio, amino, C1-C6 alkilamino, C2-C6 dialkilamino, C2-C6 alkoksikarbonil, C2-C6 alkilkarbonil, nitro, hidroksil, ili cijano;
R8 je H, etil, propil, butil, izopropil, izobutil, tercijarni butil, pentil, heksil, ciklopropil, ciklobutil, ciklopentil, cikloheksil, C2-C6 alkenil, C3-C6 alkinil, C1-C6 haloalkil, C1-C6 alkoksialkil, fenil ili benzil pri čemu svaki fenil ili benzil može biti po izboru supstituiran s 1-3 R5, ili s 5- ili 6-eročlanim zasićenim ili nezasićenim prstenastim sustavom, ili s 5-6 kondenziranim prstenastim sustavom, ili s 6-6 kondenziranim prstenastim sustavom koji svaki sadrži 1-3 heteroatoma pri čemu svaki prsten može biti po izboru supstituiran s 1-3 R5, bifenil ili naftil proizvoljno supstituiran s 1-3 R5;
R11 je H ili C1-C4 alkil;
R12 je H, cijano, hidroksil, C1-C4 alkil, C1-C6 alkoksi, C2-C6 alkilkarbonil, fenil ili benzil pri čemu svaki fenil ili benzil može biti po izboru supstituiran s 1-3 R5;
alternativno R11 i R12 se mogu uzeti zajedno tako da tvore 5- ili 6-eročlani zasićeni ili nezasićeni prsten koji sadrži 1-3 heteroatoma pri čemu svaki prsten može biti po izboru supstituiran s 1-3 R5;
R13 je H, C1-C4 alkil, C1-C6 alkoksi, C2-C6 alkilkarbonil, fenil ili benzil pri čemu svaki fenil ili benzil može biti po izboru supstituiran s 1-3 R5; i
alternativno R12 i R13 se mogu uzeti zajedno tako da tvore 5- ili 6-eročlani zasićeni ili nezasićeni prsten koji sadrži 1-3 heteroatoma pri čemu svaki prsten može biti po izboru supstituiran s 1-3 R5, ili
optički izomer, njegova sol ili hidrat,
pri čemu je alkil razgranati, nerazgranati, ili ciklički ugljikov lanac.
2. Spoj prema zahtjevu 1, naznačen time što je spoj odabran iz skupine koja sadrži:
ili optički izomer, njegova sol ili hidrat.
3. Spoj prema zahtjevu 1 ili 2 u obliku soli, naznačen time što je sol hidroklorid, hidrobromid, ili hidrojodid.
4. Pripravak za suzbijanje ili sprječavanje napada gljivičnog patogena na biljku koji sadrži spoj s formulom I:
naznačen time što R1 je:
H;
C1-C6 alkil;
benzil; ili
-C(=O)R8;
R2 je:
H; ili
C1-C6 alkil;
alternativno R1 i R2 se mogu uzeti zajedno tako da tvore =CR11N(R12)R13;
R3 je:
-C(=O)R8; ili
-C(=S)R8;
R5 je neovisno halogen, C1-C6 alkil, C1-C6 haloalkil, C1-C6 alkoksi, C1-C6 haloalkoksi, C1-C6 alkiltio, C1-C6 haloalkiltio, halotio, amino, C1-C6 alkilamino, C2-C6 dialkilamino, C2-C6 alkoksikarbonil, C2-C6 alkilkarbonil, nitro, hidroksil, ili cijano;
R8 je H, C1-C6 alkil, C2-C6 alkenil, C3-C6 alkinil, C1-C6 haloalkil, C1-C6 alkoksialkil, fenil ili benzil pri čemu svaki fenil ili benzil može biti po izboru supstituiran s 1-3 R5, ili s 5- ili 6-eročlanim zasićenim ili nezasićenim prstenastim sustavom, ili s 5-6 kondenziranim prstenastim sustavom, ili s 6-6 kondenziranim prstenastim sustavom koji svaki sadrži 1-3 heteroatoma pri čemu svaki prsten može biti po izboru supstituiran s 1-3 R5, bifenil ili naftil po izboru supstituiran s 1-3 R5;
R11 je H ili C1-C4 alkil;
R12 je H, cijano, hidroksil, C1-C4 alkil, C1-C6 alkoksi, C2-C6 alkilkarbonil, fenil ili benzil pri čemu svaki fenil ili benzil može biti po izboru supstituiran s 1-3 R5;
alternativno R11 i R12 se mogu uzeti zajedno tako da tvore 5- ili 6-eročlani zasićeni ili nezasićeni prsten koji sadrži 1-3 heteroatoma pri čemu svaki prsten može biti po izboru supstituiran s 1-3 R5;
R13 je H, C1-C4 alkil, C1-C6 alkoksi, C2-C6 alkilkarbonil, fenil ili benzil pri čemu svaki fenil ili benzil može biti po izboru supstituiran s 1-3 R5; i
alternativno R12 i R13 se mogu uzeti zajedno tako da tvore 5- ili 6-eročlani zasićeni ili nezasićeni prsten koji sadrži 1-3 heteroatoma pri čemu svaki prsten može biti po izboru supstituiran s 1-3 R5; ili
optički izomer, njegova sol ili hidrat i fitološki prihvatljiv materijal nosača,
pri čemu je alkil razgranati, nerazgranati ili ciklički ugljikov lanac.
5. Pripravak prema zahtjevi 4, naznačen time što je spoj s Formulom I u obliku soli, pri čemu je sol hidroklorid, hidrobromid, ili hidrojodid.
6. Pripravak prema zahtjevi 4 ili 5, naznačen time što je patogena gljivica krastavost jabuke (Venturia inaequalis), smeđa pjegavost pšenice (Septoria tritici), pjegavost lišća šećerne repe (Cercospora beticola), pjegavost lišća kikirikija (Cercospora arachidicola i Cercosporidium personatum), ili crna sigatoka banane (Mycosphaerella fijiensis).
7. Pripravak prema zahtjevi 6, naznačen time što je patogena gljivica smeđa pjegavost pšenice (Septoria tritici).
8. Pripravak prema bilo kojem od zahtjeva 4-7, naznačen time što pripravak također sadrži adjuvantni surfaktant.
9. Pripravak prema zahtjevi 8, naznačen time što je adjuvantni surfaktant odabran između etoksiliranih nonil fenola, etoksiliranih sintetskih ili prirodnih alkohola, soli estera ili sulfosukcinskih kiselina, etoksiliranih organosilikona, etoksiliranih masnih amina i smjesa surfaktanata s mineralnim ili biljnim uljima.
10. Pripravak prema bilo kojem od zahtjeva 4-9, naznačen time što je pripravak formuliran kao otopina, prašina, granulat, vlažni prašak, tekući koncentrat, emulgirajući koncentrat, koncentrat za suspenziju, vodena suspenzija, ili emulzija.
11. Postupak za suzbijanje ili sprječavanje napada gljivica na biljku, te postupak obuhvaća korake:
primjenu fungicidno učinkovite količine barem jednog spoja s Formulom I:
pri čemu R1 je:
H;
C1-C6 alkil;
benzil; ili
-C(=O)R8;
R2 je:
H; ili
C1-C6 alkil;
alternativno R1 i R2 se mogu uzeti zajedno tako da tvore =CR11N(R12)R13;
R3 je:
-C(=O)R8; ili
-C(=S)R8;
R5 je neovisno halogen, C1-C6 alkil, C1-C6 haloalkil, C1-C6 alkoksi, C1-C6 haloalkoksi, C1-C6 alkiltio, C1-C6 haloalkiltio, halotio, amino, C1-C6 alkilamino, C2-C6 dialkilamino, C2-C6 alkoksikarbonil, C2-C6 alkilkarbonil, nitro, hidroksil, ili cijano;
R8 je H, C1-C6 alkil, C2-C6 alkenil, C3-C6 alkinil, C1-C6 haloalkil, C1-C6 alkoksialkil, fenil ili benzil pri čemu svaki fenil ili benzil može biti po izboru supstituiran s 1-3 R5, ili sa 5- ili 6-eročlanim zasićenim ili nezasićenim prstenastim sustavom, ili s 5-6 kondenziranim prstenastim sustavom, ili s 6-6 kondenziranim prstenastim sustavom koji svaki sadrži 1-3 heteroatoma pri čemu svaki prsten može biti po izboru supstituiran s 1-3 R5, bifenilom ili naftilom proizvoljno supstituiran s 1-3 R5;
R11 je H ili C1-C4 alkil;
R12 je H, cijano, hidroksil, C1-C4 alkil, C1-C6 alkoksi, C2-C6 alkilkarbonil, fenil ili benzil pri čemu svaki fenil ili benzil može biti po izboru supstituiran s 1-3 R5;
alternativno R11 i R12 se mogu uzeti zajedno tako da tvore 5- ili 6-eročlani zasićeni ili nezasićeni prsten koji sadrži 1-3 heteroatoma pri čemu svaki prsten može biti po izboru supstituiran s 1-3 R5;
R13 je H, C1-C4 alkil, C1-C6 alkoksi, C2-C6 alkilkarbonil, fenil ili benzil pri čemu svaki fenil ili benzil može biti po izboru supstituiran s 1-3 R5;
i
alternativno R12 i R13 se mogu uzeti zajedno tako da tvore 5- ili 6-eročlani zasićeni ili nezasićeni prsten koji sadrži 1-3 heteroatoma pri čemu svaki prsten može biti po izboru supstituiran s 1-3 R5, ili
optički izomer, njegova sol ili hidrat,
na barem jedno od biljke, područje uz biljku, tlo prilagođeno da podrži rast biljke, korijen biljke, lišće biljke, i sjeme prilagođeno za proizvodnju biljke,
pri čemu je alkil razgranati, nerazgranati, ili ciklički ugljikov lanac.
12. Postupak prema zahtjevu 11, naznačen time što je spoj s Formulom I u obliku soli, pri čemu je sol hidroklorid, hidrobromid, ili hidrojodid.
13. Postupak prema zahtjevu 11 ili 12, naznačen time što je koncentracija spoja s Formulom I koja se primjenjuje od 0.1 do 1000 ppm.
14. Postupak prema bilo kojem od zahtjeva 11-13, naznačen time što je koncentracija spoja s Formulom I koja se primjenjuje od 1 do 500 ppm.
15. Postupak prema bilo kojem od zahtjeva 11-14, naznačen time što se spoj s Formulom I primjenjuje u rasponu od 0.01 do 0.45 g/m2 spoja.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23222309P | 2009-08-07 | 2009-08-07 | |
| EP10807171.3A EP2519512B1 (en) | 2009-08-07 | 2010-08-05 | N1-acyl- 5-fluoropyrimidinone derivatives |
| PCT/US2010/044576 WO2011017538A1 (en) | 2009-08-07 | 2010-08-05 | N1-acyl-5-fluoropyrimidinone derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20190919T1 true HRP20190919T1 (hr) | 2019-09-20 |
Family
ID=43535292
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HRP20190919TT HRP20190919T1 (hr) | 2009-08-07 | 2019-05-17 | Derivati n1-acil- 5-fluoropirimidinona |
Country Status (34)
| Country | Link |
|---|---|
| US (1) | US8470839B2 (hr) |
| EP (1) | EP2519512B1 (hr) |
| JP (1) | JP5748754B2 (hr) |
| KR (1) | KR101792285B1 (hr) |
| CN (1) | CN102548981B (hr) |
| AU (1) | AU2010279402B2 (hr) |
| BR (1) | BR112012002810B1 (hr) |
| CA (1) | CA2768510C (hr) |
| CL (1) | CL2012000316A1 (hr) |
| CO (1) | CO6491117A2 (hr) |
| CR (1) | CR20120030A (hr) |
| CY (1) | CY1122115T1 (hr) |
| DK (1) | DK2519512T3 (hr) |
| EA (1) | EA023411B1 (hr) |
| EC (1) | ECSP12011653A (hr) |
| ES (1) | ES2728966T3 (hr) |
| HK (1) | HK1172894A1 (hr) |
| HN (1) | HN2012000269A (hr) |
| HR (1) | HRP20190919T1 (hr) |
| HU (1) | HUE045290T2 (hr) |
| IL (1) | IL217952A (hr) |
| IN (1) | IN2012DN00539A (hr) |
| LT (1) | LT2519512T (hr) |
| MX (1) | MX2012001620A (hr) |
| NI (1) | NI201200022A (hr) |
| NZ (1) | NZ597570A (hr) |
| PE (1) | PE20120688A1 (hr) |
| PL (1) | PL2519512T3 (hr) |
| PT (1) | PT2519512T (hr) |
| SI (1) | SI2519512T1 (hr) |
| TR (1) | TR201908180T4 (hr) |
| UA (1) | UA106889C2 (hr) |
| WO (1) | WO2011017538A1 (hr) |
| ZA (1) | ZA201200819B (hr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2769073C (en) * | 2009-08-07 | 2018-07-24 | Dow Agrosciences Llc | N1-sulfonyl-5-fluoropyrimidinone derivatives |
| JP6128658B2 (ja) * | 2011-08-17 | 2017-05-17 | アダマ・マクテシム・リミテッド | ５−フルオロ−４−イミノ−３−（置換）−３，４−ジヒドロピリミジン−２−（１ｈ）−オン誘導体 |
| RU2015131149A (ru) | 2012-12-28 | 2017-02-03 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | N-(замещенные)-5-фтор-4-имино-3-метил-2-оксо-3,4-дигидропиримидин-1(2н)-карбоксамидные производные |
| MX2015008441A (es) | 2012-12-28 | 2015-09-23 | Dow Agrosciences Llc | Derivados de n-(sustituido)-5-fluoro-4-imino-3-metil-2-oxo-3, 4-dihidropirimidin-1 (2h)-carboxilato. |
| CN104994859B (zh) * | 2012-12-28 | 2018-10-26 | 阿达玛马克西姆股份有限公司 | 1-(取代的苯甲酰基)-5-氟-4-亚氨基-3-甲基-3,4-二氢嘧啶-2(1h)-酮衍生物 |
| MX2015008565A (es) | 2012-12-31 | 2015-09-07 | Dow Agrosciences Llc | Derivados de 3-alquil-5-fluoro-4-sustituido-imino-3,4-dihidropirim idin-2(1h)-ona como fungicidas. |
| WO2015103142A1 (en) | 2013-12-31 | 2015-07-09 | Dow Agrosciences Llc | 5-fluoro-4-imino-3-(alkyl/substituted alkyl)-1- (arylsulfonyl)-3,4-dihydropyrimidin-2(1h)-one and processes for their preparation |
| UA124962C2 (uk) | 2013-12-31 | 2021-12-22 | Адама Махтешім Лтд. | Синергічні фунгіцидні суміші та композиції для контролю грибків |
| CN107001397B (zh) | 2014-09-26 | 2020-10-13 | 科慕埃弗西有限公司 | 异氰酸酯衍生的有机硅烷 |
| BR112020000953A2 (pt) | 2017-07-17 | 2020-07-14 | Adama Makhteshim Ltd. | polimorfos de 5-fluoro-4-imino-3-metil-1-tosil-3,4-di-hidropirimidin-2-ona |
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| CH421973A (de) * | 1962-05-01 | 1966-10-15 | Hoffmann La Roche | Verfahren zur Herstellung eines Cytosin-Derivates |
| US3309359A (en) | 1965-10-22 | 1967-03-14 | Hoffmann La Roche | N-mono-acyl-5-fluorocytosine derivatives and process |
| US3368938A (en) * | 1966-01-13 | 1968-02-13 | Hoffmann La Roche | Controlling fungi with 5-fluorocytosine |
| US3868373A (en) | 1970-01-27 | 1975-02-25 | Hoffmann La Roche | 4-Amino-5-fluoro-2-tri(lower alkyl) silyloxypyrimidines |
| CH579057A5 (hr) | 1973-09-07 | 1976-08-31 | Hoffmann La Roche | |
| FR2530636A1 (fr) | 1982-07-23 | 1984-01-27 | Rhone Poulenc Agrochimie | Nouveaux derives de la tetrahydro-2,3,6,7 5h-thiazolo (3,2-a) pyrimidine, leur preparation et leur utilisation comme herbicides |
| EP0139613A1 (de) | 1983-08-29 | 1985-05-02 | Ciba-Geigy Ag | N-(2-Nitrophenyl)-4-aminopyrimidin-Derivate, deren Herstellung und Verwendung |
| US4845081A (en) | 1984-10-18 | 1989-07-04 | University Of Florida | Aminomethyl derivatives of biologically active substances, and enhanced delivery thereof across topical membranes |
| DE58908159D1 (de) | 1988-03-09 | 1994-09-15 | Ciba Geigy Ag | Mittel zum Schutz von Pflanzen gegen Krankheiten. |
| DE3821711A1 (de) | 1988-06-28 | 1990-02-08 | Bayer Ag | Thiazolopyrimidin-derivate, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel |
| JP3217191B2 (ja) | 1992-07-16 | 2001-10-09 | ビーエーエスエフ アクチェンゲゼルシャフト | ヘテロ芳香族化合物およびこれを含有する植物保護剤 |
| PL324486A1 (en) | 1995-07-05 | 1998-05-25 | Du Pont | Fungicidal pyrimidinones |
| CN1213373A (zh) | 1996-03-11 | 1999-04-07 | 诺瓦提斯公司 | 农药用嘧啶－4－酮衍生物 |
| HRP970239B1 (en) | 1997-05-09 | 2004-04-30 | Inst Ru Er Bouekovic | Process for the preparation of sulfonyl-pyrimidine derivatives with antitumor activity |
| GT199900185A (es) | 1998-11-06 | 2001-04-18 | Novedosa pirimidin-4-enamina como fungicida. | |
| WO2003018051A1 (en) | 2001-08-27 | 2003-03-06 | Vic Jira | Anti-fungal composition |
| JPWO2005095419A1 (ja) | 2004-04-01 | 2008-02-21 | 武田薬品工業株式会社 | チアゾロピリミジン誘導体 |
| EP2044086A2 (en) | 2006-06-30 | 2009-04-08 | Janssen Pharmaceutica N.V. | Thiazolopyrimidine modulators of trpv1 |
| US9174970B2 (en) | 2008-01-22 | 2015-11-03 | Dow Agrosciences Llc | 5-fluoro pyrimidine derivatives |
| US20100029482A1 (en) | 2008-08-01 | 2010-02-04 | Benko Zoltan L | Use of 5-fluorocytosine as a fungicide |
| CA2750413C (en) | 2009-01-23 | 2016-06-21 | Northlake Biosciences Llc | Hydroxamic acid derivatives |
| CA2769073C (en) | 2009-08-07 | 2018-07-24 | Dow Agrosciences Llc | N1-sulfonyl-5-fluoropyrimidinone derivatives |
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