JP2007506657A5 - - Google Patents
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- Publication number
- JP2007506657A5 JP2007506657A5 JP2006515917A JP2006515917A JP2007506657A5 JP 2007506657 A5 JP2007506657 A5 JP 2007506657A5 JP 2006515917 A JP2006515917 A JP 2006515917A JP 2006515917 A JP2006515917 A JP 2006515917A JP 2007506657 A5 JP2007506657 A5 JP 2007506657A5
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- optionally substituted
- formula
- halogen
- alkyl
- 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
- 125000004432 carbon atom Chemical group C* 0.000 claims 22
- 229910052736 halogen Inorganic materials 0.000 claims 13
- 150000002367 halogens Chemical class 0.000 claims 12
- 125000000623 heterocyclic group Chemical group 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- 125000000547 substituted alkyl group Chemical group 0.000 claims 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
- 229910052794 bromium Inorganic materials 0.000 claims 4
- 239000000460 chlorine Substances 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 239000001301 oxygen Substances 0.000 claims 4
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 4
- KVGVQTOQSNJTJI-UHFFFAOYSA-N 8-azaxanthine Chemical class O=C1NC(=O)NC2=C1NN=N2 KVGVQTOQSNJTJI-UHFFFAOYSA-N 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 3
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 3
- -1 cyano, hydroxy Chemical group 0.000 claims 3
- 239000003085 diluting agent Substances 0.000 claims 3
- 229910052731 fluorine Inorganic materials 0.000 claims 3
- 239000011737 fluorine Substances 0.000 claims 3
- 244000005700 microbiome Species 0.000 claims 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- JSIAIROWMJGMQZ-UHFFFAOYSA-N 2h-triazol-4-amine Chemical class NC1=CNN=N1 JSIAIROWMJGMQZ-UHFFFAOYSA-N 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000004666 alkoxyiminoalkyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 230000002140 halogenating effect Effects 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 1
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 1
- 125000004426 substituted alkynyl group Chemical group 0.000 claims 1
- YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical compound BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 claims 1
- 0 *c1n[n]2c(*)c(*)c(*)nc2n1 Chemical compound *c1n[n]2c(*)c(*)c(*)nc2n1 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10328173A DE10328173A1 (de) | 2003-06-24 | 2003-06-24 | Triazolopyrimidine |
| PCT/EP2004/006369 WO2004113341A2 (de) | 2003-06-24 | 2004-06-14 | Fungizide triazolopyrimidine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007506657A JP2007506657A (ja) | 2007-03-22 |
| JP2007506657A5 true JP2007506657A5 (enExample) | 2007-08-02 |
Family
ID=33520827
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006515917A Pending JP2007506657A (ja) | 2003-06-24 | 2004-06-14 | 殺真菌性トリアゾロピリミジン類 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20060281767A1 (enExample) |
| EP (1) | EP1638974A2 (enExample) |
| JP (1) | JP2007506657A (enExample) |
| KR (1) | KR20060024432A (enExample) |
| CN (1) | CN1809571A (enExample) |
| BR (1) | BRPI0411972A (enExample) |
| CO (1) | CO5650198A2 (enExample) |
| DE (1) | DE10328173A1 (enExample) |
| MX (1) | MXPA05013743A (enExample) |
| WO (1) | WO2004113341A2 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2131658A2 (en) * | 2007-01-30 | 2009-12-16 | Basf Se | Method for improving plant health |
| US12428400B2 (en) | 2020-06-01 | 2025-09-30 | Unimatec Co., Ltd. | Fluorine-containing fused ring pyrimidine compound and method for producing same |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL108747A (en) * | 1993-03-04 | 1999-03-12 | Shell Int Research | Mushroom-killing preparations containing a history of 6 metamorphoses of 5 - 7 Dihalo - 1, 2 - 4 Triazlo [A-1,5] Pyrimidine Certain such new compounds and their preparation |
| IL108731A (en) * | 1993-03-04 | 1997-03-18 | Shell Int Research | 6, N-DISUBSTITUTED-£1, 2, 4| TRIAZOLO-£1, 5-a| PYRIMIDINE- 7-AMINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS FUNGICIDES |
| US6277857B1 (en) * | 1998-09-25 | 2001-08-21 | American Cyanamid Company | Fungicidal 7-oxy-and 7-thio-substituted-triazolopyrimidines |
| PL360027A1 (en) * | 2000-06-30 | 2004-09-06 | Wyeth | Substituted-triazolopyrimidines as anticancer agents |
| US6737085B2 (en) * | 2000-11-01 | 2004-05-18 | Tokiwa Phytochemical Co., Ltd. | Apocynum venetum extract for use as antidepressant |
| DE10063115A1 (de) * | 2000-12-18 | 2002-06-27 | Bayer Ag | Triazolopyrimidine |
| DE10121162A1 (de) * | 2001-04-30 | 2002-10-31 | Bayer Ag | Triazolopyrimidine |
| GB0126914D0 (en) * | 2001-11-08 | 2002-01-02 | Syngenta Ltd | Fungicides |
| US6576411B1 (en) * | 2001-11-21 | 2003-06-10 | Eastman Kodak Company | Method of passivating a silver donor with a dye and photothermographic systems made thereby |
| WO2004011467A1 (ja) * | 2002-07-29 | 2004-02-05 | Hokko Chemical Industry Co., Ltd. | トリアゾロピリミジン誘導体および農園芸用殺菌剤 |
-
2003
- 2003-06-24 DE DE10328173A patent/DE10328173A1/de not_active Withdrawn
-
2004
- 2004-06-14 MX MXPA05013743A patent/MXPA05013743A/es unknown
- 2004-06-14 EP EP04739853A patent/EP1638974A2/de not_active Withdrawn
- 2004-06-14 WO PCT/EP2004/006369 patent/WO2004113341A2/de not_active Ceased
- 2004-06-14 CN CNA2004800175462A patent/CN1809571A/zh active Pending
- 2004-06-14 KR KR1020057024438A patent/KR20060024432A/ko not_active Withdrawn
- 2004-06-14 JP JP2006515917A patent/JP2007506657A/ja active Pending
- 2004-06-14 BR BRPI0411972-0A patent/BRPI0411972A/pt not_active IP Right Cessation
- 2004-06-14 US US10/561,174 patent/US20060281767A1/en not_active Abandoned
-
2005
- 2005-12-21 CO CO05128694A patent/CO5650198A2/es not_active Application Discontinuation
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