JP2007502312A5 - - Google Patents
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- Publication number
- JP2007502312A5 JP2007502312A5 JP2006529790A JP2006529790A JP2007502312A5 JP 2007502312 A5 JP2007502312 A5 JP 2007502312A5 JP 2006529790 A JP2006529790 A JP 2006529790A JP 2006529790 A JP2006529790 A JP 2006529790A JP 2007502312 A5 JP2007502312 A5 JP 2007502312A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- haloalkyl
- chlorine
- alkoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000460 chlorine Substances 0.000 claims 36
- 229910052801 chlorine Inorganic materials 0.000 claims 35
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 28
- 239000011737 fluorine Substances 0.000 claims 28
- 229910052731 fluorine Inorganic materials 0.000 claims 28
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 26
- 229910052736 halogen Inorganic materials 0.000 claims 23
- 125000001424 substituent group Chemical group 0.000 claims 23
- 125000005843 halogen group Chemical group 0.000 claims 21
- 125000004432 carbon atom Chemical group C* 0.000 claims 20
- 229910052739 hydrogen Inorganic materials 0.000 claims 20
- 239000001257 hydrogen Substances 0.000 claims 20
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 19
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 17
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 16
- 125000000753 cycloalkyl group Chemical group 0.000 claims 15
- 125000001246 bromo group Chemical group Br* 0.000 claims 13
- -1 cyano, nitro, amino, hydroxyl Chemical group 0.000 claims 13
- 150000002431 hydrogen Chemical class 0.000 claims 13
- 239000003085 diluting agent Substances 0.000 claims 11
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 10
- 229910052794 bromium Inorganic materials 0.000 claims 10
- CRLKPYDHBFGVFB-UHFFFAOYSA-N 2-(difluoromethyl)-n-phenylbenzamide Chemical compound FC(F)C1=CC=CC=C1C(=O)NC1=CC=CC=C1 CRLKPYDHBFGVFB-UHFFFAOYSA-N 0.000 claims 9
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 8
- 125000000623 heterocyclic group Chemical group 0.000 claims 8
- 239000011630 iodine Chemical group 0.000 claims 8
- 229910052740 iodine Inorganic materials 0.000 claims 8
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
- 239000002253 acid Substances 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 6
- 150000002367 halogens Chemical class 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 239000011230 binding agent Substances 0.000 claims 5
- 239000003054 catalyst Substances 0.000 claims 5
- 125000001188 haloalkyl group Chemical group 0.000 claims 5
- 244000005700 microbiome Species 0.000 claims 5
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 claims 5
- WGLLSSPDPJPLOR-UHFFFAOYSA-N 2,3-dimethylbut-2-ene Chemical group CC(C)=C(C)C WGLLSSPDPJPLOR-UHFFFAOYSA-N 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 3
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims 3
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims 3
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims 2
- 239000004067 bulking agent Substances 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 125000006413 ring segment Chemical group 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 1
- VZLPLYDPKXQAIA-UHFFFAOYSA-N 2-(difluoromethyl)benzonitrile Chemical compound FC(F)C1=CC=CC=C1C#N VZLPLYDPKXQAIA-UHFFFAOYSA-N 0.000 claims 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- 125000001054 5 membered carbocyclic group Chemical group 0.000 claims 1
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 claims 1
- 150000001345 alkine derivatives Chemical class 0.000 claims 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000005087 alkynylcarbonyl group Chemical group 0.000 claims 1
- 125000005133 alkynyloxy group Chemical group 0.000 claims 1
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 150000001642 boronic acid derivatives Chemical class 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000012320 chlorinating reagent Substances 0.000 claims 1
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 1
- 230000018044 dehydration Effects 0.000 claims 1
- 238000006297 dehydration reaction Methods 0.000 claims 1
- 125000004983 dialkoxyalkyl group Chemical group 0.000 claims 1
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 1
- 125000005202 dialkylaminocarbonyloxy group Chemical group 0.000 claims 1
- CSJLBAMHHLJAAS-UHFFFAOYSA-N diethylaminosulfur trifluoride Chemical compound CCN(CC)S(F)(F)F CSJLBAMHHLJAAS-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 125000000262 haloalkenyl group Chemical group 0.000 claims 1
- 125000005291 haloalkenyloxy group Chemical group 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 1
- 125000004995 haloalkylthio group Chemical group 0.000 claims 1
- 150000002430 hydrocarbons Chemical group 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 125000005188 oxoalkyl group Chemical group 0.000 claims 1
- 125000005702 oxyalkylene group Chemical group 0.000 claims 1
- 229910052763 palladium Inorganic materials 0.000 claims 1
- 125000003884 phenylalkyl group Chemical group 0.000 claims 1
- 125000004660 phenylalkylthio group Chemical group 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 0 *c(c(*)c1*)c(*)c(*)c1N* Chemical compound *c(c(*)c1*)c(*)c(*)c1N* 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10322909 | 2003-05-21 | ||
| DE10325438A DE10325438A1 (de) | 2003-05-21 | 2003-06-05 | Difluormethylbenzanilide |
| PCT/EP2004/005067 WO2004103953A1 (de) | 2003-05-21 | 2004-05-12 | Difluormethylbenzanilide und deren verwendung zur bekämpfung bon mikroorganismen, sowie zwischen produkte und deren herstellung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007502312A JP2007502312A (ja) | 2007-02-08 |
| JP2007502312A5 true JP2007502312A5 (cg-RX-API-DMAC7.html) | 2007-07-12 |
Family
ID=33477511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006529790A Pending JP2007502312A (ja) | 2003-05-21 | 2004-05-12 | ジフロオロメチルベンズアニリド類 |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP1628948A1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2007502312A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20060017605A (cg-RX-API-DMAC7.html) |
| AU (1) | AU2004240721A1 (cg-RX-API-DMAC7.html) |
| BR (1) | BRPI0410443A (cg-RX-API-DMAC7.html) |
| CA (1) | CA2526358A1 (cg-RX-API-DMAC7.html) |
| MX (1) | MXPA05012438A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2004103953A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10352067A1 (de) * | 2003-10-23 | 2005-05-25 | Bayer Cropscience Ag | Isopentylcarboxanilide |
| DE102005009457A1 (de) * | 2005-03-02 | 2006-09-07 | Bayer Cropscience Ag | Verfahren zum Herstellen von Alkylaniliden |
| DE102005022147A1 (de) * | 2005-04-28 | 2006-11-02 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| US10183948B2 (en) | 2013-03-29 | 2019-01-22 | Ogeda Sa | N-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists |
| JP6316932B2 (ja) | 2013-03-29 | 2018-04-25 | オゲダ エス．エー． | 選択的ＮＫ−３受容体拮抗薬としての新規なＮ−アシル−（３位置換）−（８位置換）−５，６−ジヒドロ−［１，２，４］トリアゾロ［４，３−ａ］ピラジン、医薬組成物、ＮＫ−３受容体媒介性障害における使用方法 |
| CN111699182A (zh) * | 2018-01-17 | 2020-09-22 | 米加尔-加利里研究院有限公司 | 新型蛋氨酸代谢途径抑制剂 |
| CN111662269B (zh) * | 2019-03-07 | 2021-05-07 | 湖南化工研究院有限公司 | 1-吡啶基吡唑酰胺类化合物及其制备方法与应用 |
| WO2021001825A1 (en) * | 2019-07-04 | 2021-01-07 | Migal Galilee Research Institute Ltd. | Methionine metabolic pathway inhibitors |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2369252B1 (fr) * | 1976-10-29 | 1979-02-23 | Inst Nat Rech Chimique | Composes a,a-difluoroalkylbenzenes substitues et leur fabricationÿ |
| JPS53132536A (en) * | 1977-04-21 | 1978-11-18 | Nippon Nohyaku Co Ltd | Benzanilides, their preparation, and agricultural and horticultural fungicide containing the same |
| JPS6021135B2 (ja) * | 1977-05-02 | 1985-05-25 | 日本農薬株式会社 | トルイル酸アニリド類及びその製造方法並びにそれを含有する農園芸用殺菌剤 |
| JPS54107521A (en) * | 1978-02-10 | 1979-08-23 | Nippon Nohyaku Co Ltd | Agricultural and horticultural bactericidal composition |
| JPS5531048A (en) * | 1978-08-28 | 1980-03-05 | Kumiai Chem Ind Co Ltd | Agricultural and horticultural fungicide composition |
| CA2081935C (en) * | 1991-11-22 | 2004-05-25 | Karl Eicken | Anilide derivatives and their use for combating botrytis |
| US5223526A (en) * | 1991-12-06 | 1993-06-29 | Monsanto Company | Pyrazole carboxanilide fungicides and use |
| DE4231517A1 (de) * | 1992-09-21 | 1994-03-24 | Basf Ag | Carbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
| DE19629828A1 (de) * | 1996-07-24 | 1998-01-29 | Bayer Ag | Carbanilide |
| JP3982879B2 (ja) * | 1996-08-15 | 2007-09-26 | 三井化学株式会社 | 置換カルボン酸アニリド誘導体およびこれを有効成分とする植物病害防除剤 |
| CZ20021890A3 (cs) * | 1999-12-09 | 2002-08-14 | Syngenta Participations Ag | Pyrazolkarboxamidy a pyrazolthioamidy, způsob jejich přípravy a jejich pouľití jako fungicidních prostředků |
| GB0001447D0 (en) * | 2000-01-21 | 2000-03-08 | Novartis Ag | Organic compounds |
| JP2001302605A (ja) * | 2000-04-20 | 2001-10-31 | Sumitomo Chem Co Ltd | ビフェニル化合物およびその用途 |
| MXPA03000688A (es) * | 2000-07-24 | 2004-11-01 | Bayer Cropscience Ag | Bifenilcarboxiamidas. |
| DE10122447A1 (de) * | 2000-07-24 | 2002-04-18 | Bayer Ag | Biphenylcarboxamide |
| GB0101996D0 (en) * | 2001-01-25 | 2001-03-14 | Syngenta Participations Ag | Organtic compounds |
| GB0103258D0 (en) * | 2001-02-09 | 2001-03-28 | Syngenta Participations Ag | Organic compounds |
-
2004
- 2004-05-12 WO PCT/EP2004/005067 patent/WO2004103953A1/de not_active Ceased
- 2004-05-12 MX MXPA05012438A patent/MXPA05012438A/es not_active Application Discontinuation
- 2004-05-12 BR BRPI0410443-9A patent/BRPI0410443A/pt not_active IP Right Cessation
- 2004-05-12 AU AU2004240721A patent/AU2004240721A1/en not_active Abandoned
- 2004-05-12 KR KR1020057021271A patent/KR20060017605A/ko not_active Withdrawn
- 2004-05-12 EP EP04732289A patent/EP1628948A1/de not_active Withdrawn
- 2004-05-12 CA CA002526358A patent/CA2526358A1/en not_active Abandoned
- 2004-05-12 JP JP2006529790A patent/JP2007502312A/ja active Pending
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