JP2011063599A5 - - Google Patents
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- Publication number
- JP2011063599A5 JP2011063599A5 JP2010243111A JP2010243111A JP2011063599A5 JP 2011063599 A5 JP2011063599 A5 JP 2011063599A5 JP 2010243111 A JP2010243111 A JP 2010243111A JP 2010243111 A JP2010243111 A JP 2010243111A JP 2011063599 A5 JP2011063599 A5 JP 2011063599A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- alkyl
- formula
- fluorine
- hydrogen
- 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.)
- Withdrawn
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- -1 methyl- Chemical group 0.000 claims 31
- 150000001875 compounds Chemical class 0.000 claims 8
- 229910052739 hydrogen Inorganic materials 0.000 claims 8
- 239000001257 hydrogen Substances 0.000 claims 8
- 125000001424 substituent group Chemical group 0.000 claims 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 7
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 238000004519 manufacturing process Methods 0.000 claims 7
- 239000011737 fluorine Substances 0.000 claims 6
- 229910052731 fluorine Inorganic materials 0.000 claims 6
- 239000000460 chlorine Substances 0.000 claims 5
- 229910052801 chlorine Inorganic materials 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 239000003085 diluting agent Substances 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 3
- DAFQZPUISLXFBF-UHFFFAOYSA-N tetraoxathiolane 5,5-dioxide Chemical compound O=S1(=O)OOOO1 DAFQZPUISLXFBF-UHFFFAOYSA-N 0.000 claims 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 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
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 claims 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 125000005137 alkenylsulfonyl group Chemical group 0.000 claims 1
- 125000004369 butenyl group Chemical group C(=CCC)* 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
- JZBWUTVDIDNCMW-UHFFFAOYSA-L dipotassium;oxido sulfate Chemical group [K+].[K+].[O-]OS([O-])(=O)=O JZBWUTVDIDNCMW-UHFFFAOYSA-L 0.000 claims 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- 125000006260 ethylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims 1
- 125000006351 ethylthiomethyl group Chemical group [H]C([H])([H])C([H])([H])SC([H])([H])* 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000004995 haloalkylthio group Chemical group 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 1
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 claims 1
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- HJKYXKSLRZKNSI-UHFFFAOYSA-I pentapotassium;hydrogen sulfate;oxido sulfate;sulfuric acid Chemical compound [K+].[K+].[K+].[K+].[K+].OS([O-])(=O)=O.[O-]S([O-])(=O)=O.OS(=O)(=O)O[O-].OS(=O)(=O)O[O-] HJKYXKSLRZKNSI-UHFFFAOYSA-I 0.000 claims 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims 1
- 229910052717 sulfur Chemical group 0.000 claims 1
- 239000011593 sulfur Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 0 *C(CCS*)=C(F)F Chemical compound *C(CCS*)=C(F)F 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10229776A DE10229776A1 (de) | 2002-07-03 | 2002-07-03 | Verfahren zum Herstellen von heterocyclischen Fluoralkenylsulfonen |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004518547A Division JP4753579B2 (ja) | 2002-07-03 | 2003-06-20 | ヘテロ環式フルオロアルケニルスルホンの製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011063599A JP2011063599A (ja) | 2011-03-31 |
| JP2011063599A5 true JP2011063599A5 (https=) | 2012-01-26 |
Family
ID=29761584
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004518547A Expired - Fee Related JP4753579B2 (ja) | 2002-07-03 | 2003-06-20 | ヘテロ環式フルオロアルケニルスルホンの製造方法 |
| JP2010243111A Withdrawn JP2011063599A (ja) | 2002-07-03 | 2010-10-29 | ヘテロ環式フルオロアルケニルスルホンの製造方法 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004518547A Expired - Fee Related JP4753579B2 (ja) | 2002-07-03 | 2003-06-20 | ヘテロ環式フルオロアルケニルスルホンの製造方法 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US8901311B2 (https=) |
| EP (2) | EP2258693A1 (https=) |
| JP (2) | JP4753579B2 (https=) |
| KR (1) | KR100874238B1 (https=) |
| CN (2) | CN104761512A (https=) |
| AU (1) | AU2003245974A1 (https=) |
| CY (1) | CY1115410T1 (https=) |
| DE (1) | DE10229776A1 (https=) |
| DK (1) | DK1519928T3 (https=) |
| ES (1) | ES2485842T3 (https=) |
| MX (1) | MXPA05000121A (https=) |
| PT (1) | PT1519928E (https=) |
| SI (1) | SI1519928T1 (https=) |
| WO (1) | WO2004005268A1 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10319590A1 (de) | 2003-05-02 | 2004-11-18 | Bayer Cropscience Ag | Wirkstoffkombinationen mit nematiziden und insektiziden Eigenschaften basierend auf Trifluorbutenyl-Verbindungen |
| DE10319591A1 (de) | 2003-05-02 | 2004-11-18 | Bayer Cropscience Ag | Wirkstoffkombinationen mit nematiziden, insektiziden und fungiziden Eigenschaften basierend auf Trifluorbutenyl-Verbindungen |
| CN102702133A (zh) * | 2012-01-10 | 2012-10-03 | 山东省联合农药工业有限公司 | 一种含噻唑的三氟丁烯类杀虫剂 |
| CN103012386B (zh) * | 2012-12-26 | 2015-04-01 | 浙江普洛得邦制药有限公司 | 一种五元环状硫酸酯的制备方法 |
| BR122022001868B1 (pt) | 2015-12-10 | 2022-09-13 | Adama Makhteshim Ltd. | Composição de material agrícola, método de controle e prevenção de peste e de aperfeiçoamento do crescimento de planta, processo de preparo da composição de material agrícola e uso de um copolímero em bloco |
| US10792633B2 (en) | 2016-02-25 | 2020-10-06 | Hwk-Kronbichler Gmbh | Composition comprising a fluorine-containing surfactant |
| IL267063A (en) * | 2016-12-09 | 2019-07-30 | Adama Makhteshim Ltd | Fluensulfone formulations in high concentration, their uses and processes for their preparation |
| JP2021507911A (ja) * | 2017-12-20 | 2021-02-25 | ピーアイ インダストリーズ リミテッドＰｉ Ｉｎｄｕｓｔｒｉｅｓ Ｌｔｄ | フルオロアルケニル化合物、その製造法およびその使用 |
| AR114185A1 (es) * | 2018-01-23 | 2020-07-29 | Adama Makhteshim Ltd | Síntesis de 5-cloro-2-[(3,4,4-trifluoro-3-buten-1-il)tio]-tiazol |
| AR116506A1 (es) | 2018-09-26 | 2021-05-12 | Adama Makhteshim Ltd | Proceso e intermediarios para la preparación de fluensulfona |
| WO2020095161A1 (en) | 2018-11-05 | 2020-05-14 | Pi Industries Ltd. | Nitrone compounds and use thereof |
| AR117551A1 (es) * | 2018-12-31 | 2021-08-11 | Adama Makhteshim Ltd | Síntesis de 1,1,2-trifluoro-4-(sulfonil sustituido)-but-1-eno |
| WO2021024253A1 (en) | 2019-08-04 | 2021-02-11 | Yeda Research And Development Co. Ltd. | Process for the preparation of fluensulfone |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3513172A (en) | 1965-09-27 | 1970-05-19 | Stauffer Chemical Co | 3-phenyl-5-(3,4,4-trifluoro-3-butenylthio)1,2,4-thiadiazole |
| US3697538A (en) | 1968-06-03 | 1972-10-10 | Synvar Ass | 2,4,5-substituted n-oxy and hydroxyimidazoles |
| HU204022B (en) | 1985-06-20 | 1991-11-28 | Fmc Corp | Nematocidal compositions comprising polyhalogen alkene derivatives and process for producing polyhalogen alkene derivatives |
| CN1100092A (zh) | 1992-12-23 | 1995-03-15 | 史密丝克莱恩比彻姆公司 | 砜的制备方法 |
| US5274139A (en) | 1993-02-26 | 1993-12-28 | University Of Florida | Method for effective reaction between oxygen and organic substance utilizing regenerable hydroperioxide oxidant |
| IL112721A0 (en) | 1994-03-10 | 1995-05-26 | Zeneca Ltd | Azole derivatives |
| GB2293380A (en) | 1994-09-22 | 1996-03-27 | Zeneca Ltd | Pesticidal heterocyclic and phenyl compounds |
| GB9708280D0 (en) | 1997-04-24 | 1997-06-18 | Zeneca Ltd | Novel process |
| CA2254579C (en) | 1997-12-12 | 2007-10-30 | Bayer Corporation | Synthesis of 2-(methylsulfonyl)-5-(trifluoromethyl)-1,3,4-thiadiazole via oxidation of 2-(methylthio)-5-(trifluoromethyl)-1,3,4-thiadiazole with a molybdenum or tungsten catalyst |
| US6031108A (en) | 1998-09-16 | 2000-02-29 | Bayer Corporation | Process for the preparation of 2-(methylsulfonyl)-5-(trifluoromethyl)-1,3,4-thiadiazole (TDA sulfone) |
| US5965737A (en) | 1999-02-17 | 1999-10-12 | Bayer Corporation | Approach to the conversion of 2-(methylthio)-5-(trifluoromethyl)-1,3,4-thiadiazole (TDA) to 2-(methylsulfonyl)-5-(trifluoromethyl)-1,3,4-thiadiazole (TDA sulfone) |
| JP2001019685A (ja) * | 1999-07-06 | 2001-01-23 | Nippon Bayer Agrochem Co Ltd | 殺センチュウ性トリフルオロブテン類 |
| JP2001322988A (ja) | 2000-03-09 | 2001-11-20 | Nippon Bayer Agrochem Co Ltd | 殺センチュウ性トリフルオロブテン類 |
| DE10031088C2 (de) | 2000-06-30 | 2002-12-19 | Raymond A & Cie | Beheizbare Scheibenwaschdüse |
| DE10034130A1 (de) | 2000-07-13 | 2002-01-24 | Bayer Ag | Heterocyclische Fluoralkenylthioether (lV) |
| DE10034132A1 (de) | 2000-07-13 | 2002-01-24 | Bayer Ag | Heterocyclische Fluoralkenylthioether (lll) |
| DE10034131A1 (de) | 2000-07-13 | 2002-01-24 | Bayer Ag | Heterocyclische Fluoralkenylthioether (II) |
| DE10034133A1 (de) | 2000-07-13 | 2002-01-24 | Bayer Ag | Heterocyclische Fluoralkenylthioether (l) |
| DE10201238A1 (de) | 2002-01-15 | 2003-07-24 | Bayer Cropscience Ag | Verfahren zur Herstellung von halogenierten 2-(3-Butenylsulfanyl)-1,3-thiazolen |
| TWI270542B (en) | 2002-02-07 | 2007-01-11 | Sumitomo Chemical Co | Method for preparing sulfone or sulfoxide compound |
-
2002
- 2002-07-03 DE DE10229776A patent/DE10229776A1/de not_active Withdrawn
-
2003
- 2003-06-20 AU AU2003245974A patent/AU2003245974A1/en not_active Abandoned
- 2003-06-20 JP JP2004518547A patent/JP4753579B2/ja not_active Expired - Fee Related
- 2003-06-20 SI SI200332366T patent/SI1519928T1/sl unknown
- 2003-06-20 DK DK03738072.2T patent/DK1519928T3/da active
- 2003-06-20 EP EP10178611A patent/EP2258693A1/de not_active Withdrawn
- 2003-06-20 PT PT37380722T patent/PT1519928E/pt unknown
- 2003-06-20 WO PCT/EP2003/006511 patent/WO2004005268A1/de not_active Ceased
- 2003-06-20 CN CN201510100450.2A patent/CN104761512A/zh active Pending
- 2003-06-20 CN CN038157225A patent/CN1665795A/zh active Pending
- 2003-06-20 ES ES03738072.2T patent/ES2485842T3/es not_active Expired - Lifetime
- 2003-06-20 US US10/518,454 patent/US8901311B2/en not_active Expired - Lifetime
- 2003-06-20 MX MXPA05000121A patent/MXPA05000121A/es unknown
- 2003-06-20 EP EP03738072.2A patent/EP1519928B1/de not_active Expired - Lifetime
- 2003-06-20 KR KR1020047020932A patent/KR100874238B1/ko not_active Expired - Fee Related
-
2010
- 2010-10-29 JP JP2010243111A patent/JP2011063599A/ja not_active Withdrawn
-
2014
- 2014-07-28 CY CY20141100567T patent/CY1115410T1/el unknown
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