JP2003525275A5 - - Google Patents
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- Publication number
- JP2003525275A5 JP2003525275A5 JP2001563493A JP2001563493A JP2003525275A5 JP 2003525275 A5 JP2003525275 A5 JP 2003525275A5 JP 2001563493 A JP2001563493 A JP 2001563493A JP 2001563493 A JP2001563493 A JP 2001563493A JP 2003525275 A5 JP2003525275 A5 JP 2003525275A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- halogen
- haloalkyl
- hydrogen
- 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.)
- Granted
Links
- 229910052739 hydrogen Inorganic materials 0.000 description 32
- 239000001257 hydrogen Substances 0.000 description 32
- 125000000217 alkyl group Chemical group 0.000 description 31
- 229910052736 halogen Inorganic materials 0.000 description 30
- 150000002367 halogens Chemical class 0.000 description 30
- 125000001188 haloalkyl group Chemical group 0.000 description 25
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 21
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 16
- 125000003545 alkoxy group Chemical group 0.000 description 14
- 150000002431 hydrogen Chemical class 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 125000004438 haloalkoxy group Chemical group 0.000 description 8
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 125000000753 cycloalkyl group Chemical group 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 125000001624 naphthyl group Chemical group 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 0 C*Cc1c(*)[n](*)nc1C#N Chemical compound C*Cc1c(*)[n](*)nc1C#N 0.000 description 4
- 125000000304 alkynyl group Chemical group 0.000 description 4
- 125000000232 haloalkynyl group Chemical group 0.000 description 4
- 125000000262 haloalkenyl group Chemical group 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 230000000361 pesticidal effect Effects 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18631300P | 2000-03-02 | 2000-03-02 | |
| US60/186,313 | 2000-03-02 | ||
| PCT/EP2001/002306 WO2001064651A1 (en) | 2000-03-02 | 2001-03-01 | 3-thiomethylpyrazoles as pesticides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003525275A JP2003525275A (ja) | 2003-08-26 |
| JP2003525275A5 true JP2003525275A5 (https=) | 2011-11-24 |
| JP4864269B2 JP4864269B2 (ja) | 2012-02-01 |
Family
ID=22684448
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001563493A Expired - Lifetime JP4864269B2 (ja) | 2000-03-02 | 2001-03-01 | 農薬としての３−チオメチルピラゾール |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6458744B2 (https=) |
| EP (1) | EP1263734B1 (https=) |
| JP (1) | JP4864269B2 (https=) |
| AR (1) | AR035912A1 (https=) |
| AT (1) | ATE340163T1 (https=) |
| AU (1) | AU2001246489A1 (https=) |
| CO (1) | CO5221057A1 (https=) |
| CY (1) | CY1107485T1 (https=) |
| DE (1) | DE60123219T2 (https=) |
| DK (1) | DK1263734T3 (https=) |
| ES (1) | ES2273820T3 (https=) |
| PT (1) | PT1263734E (https=) |
| WO (1) | WO2001064651A1 (https=) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6663876B2 (en) * | 2002-04-29 | 2003-12-16 | Piedmont Pharmaceuticals, Llc | Methods and compositions for treating ectoparasite infestation |
| US7396850B2 (en) * | 2003-01-06 | 2008-07-08 | Eli Lilly And Company | Pyrazole derivative as PPAR modulator |
| JP4621939B2 (ja) * | 2004-03-31 | 2011-02-02 | イハラケミカル工業株式会社 | ５−ヒドロキシ−４−チオメチルピラゾール化合物の製造方法 |
| CA2657247A1 (en) | 2006-07-28 | 2008-01-31 | Boehringer Ingelheim International Gmbh | Compounds which modulate the cb2 receptor |
| US7928123B2 (en) | 2006-09-25 | 2011-04-19 | Boehringer Ingelheim International Gmbh | Compounds which modulate the CB2 receptor |
| EP2167464B1 (en) * | 2007-05-25 | 2014-12-03 | AbbVie Deutschland GmbH & Co KG | Heterocyclic compounds as positive modulators of metabotropic glutamate receptor 2 (mglu2 receptor) |
| WO2009075080A1 (ja) * | 2007-12-10 | 2009-06-18 | Kumiai Chemical Industry Co., Ltd. | フルオロアルキルスルフィド誘導体及び有害生物防除剤 |
| EP2418207A1 (en) * | 2008-05-13 | 2012-02-15 | Boehringer Ingelheim International GmbH | Sulfone compounds which modulate the CB2 receptor |
| CA2737639A1 (en) | 2008-09-25 | 2010-04-01 | Boehringer Ingelheim International Gmbh | Compounds which selectively modulate the cb2 receptor |
| WO2011088015A1 (en) | 2010-01-15 | 2011-07-21 | Boehringer Ingelheim International Gmbh | Compounds which modulate the cb2 receptor |
| WO2012012307A1 (en) | 2010-07-22 | 2012-01-26 | Boehringer Ingelheim International Gmbh | Sulfonyl compounds which modulate the cb2 rece |
| EP2803668A1 (en) | 2013-05-17 | 2014-11-19 | Boehringer Ingelheim International Gmbh | Novel (cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6210067A (ja) * | 1985-07-05 | 1987-01-19 | Ube Ind Ltd | 新規ピラゾ−ル誘導体及びこれを含む殺虫・殺ダニ剤 |
| GB8531485D0 (en) | 1985-12-20 | 1986-02-05 | May & Baker Ltd | Compositions of matter |
| GB8713768D0 (en) | 1987-06-12 | 1987-07-15 | May & Baker Ltd | Compositions of matter |
| DE3706993A1 (de) * | 1987-03-05 | 1988-09-15 | Bayer Ag | 5-amino-3-halogenalkyl-1-aryl-pyrazole |
| GB8816915D0 (en) | 1988-07-15 | 1988-08-17 | May & Baker Ltd | New compositions of matter |
| IL101702A (en) | 1991-04-30 | 1996-03-31 | Rhone Poulenc Agrochimie | 1-aryl-5-(substituted alkylideneimino)-pyrazoles process for their preparation and arthropodicidal nematodicidal helminthicidal and protozoocidal compositions containing them |
| DE4343832A1 (de) * | 1993-12-22 | 1995-06-29 | Bayer Ag | Substituierte 1-Arylpyrazole |
| JPH08311036A (ja) * | 1995-03-14 | 1996-11-26 | Takeda Chem Ind Ltd | ピラゾール誘導体、その用途 |
| JPH11171702A (ja) * | 1997-09-24 | 1999-06-29 | Takeda Chem Ind Ltd | 害虫防除方法 |
-
2001
- 2001-02-28 CO CO01015783A patent/CO5221057A1/es not_active Application Discontinuation
- 2001-02-28 AR ARP010100948A patent/AR035912A1/es unknown
- 2001-03-01 EP EP01919359A patent/EP1263734B1/en not_active Expired - Lifetime
- 2001-03-01 PT PT01919359T patent/PT1263734E/pt unknown
- 2001-03-01 ES ES01919359T patent/ES2273820T3/es not_active Expired - Lifetime
- 2001-03-01 DE DE60123219T patent/DE60123219T2/de not_active Expired - Lifetime
- 2001-03-01 WO PCT/EP2001/002306 patent/WO2001064651A1/en not_active Ceased
- 2001-03-01 AU AU2001246489A patent/AU2001246489A1/en not_active Abandoned
- 2001-03-01 JP JP2001563493A patent/JP4864269B2/ja not_active Expired - Lifetime
- 2001-03-01 AT AT01919359T patent/ATE340163T1/de active
- 2001-03-01 DK DK01919359T patent/DK1263734T3/da active
- 2001-03-02 US US09/796,651 patent/US6458744B2/en not_active Expired - Lifetime
-
2006
- 2006-09-26 CY CY20061101382T patent/CY1107485T1/el unknown
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