AU2003210217A1 - 2-(2-pyridyl)-5-phenyl-6-aminopyrimidine, method and intermediate products for the production and use thereof for combating noxious fungi - Google Patents
2-(2-pyridyl)-5-phenyl-6-aminopyrimidine, method and intermediate products for the production and use thereof for combating noxious fungiInfo
- Publication number
- AU2003210217A1 AU2003210217A1 AU2003210217A AU2003210217A AU2003210217A1 AU 2003210217 A1 AU2003210217 A1 AU 2003210217A1 AU 2003210217 A AU2003210217 A AU 2003210217A AU 2003210217 A AU2003210217 A AU 2003210217A AU 2003210217 A1 AU2003210217 A1 AU 2003210217A1
- Authority
- AU
- Australia
- Prior art keywords
- sup
- alkyl
- halogenalkyl
- halogen
- represents 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.)
- Abandoned
Links
- 239000013067 intermediate product Substances 0.000 title abstract 2
- BGCZFXZLBAWKGX-UHFFFAOYSA-N 5-phenyl-2-pyridin-2-ylpyrimidin-4-amine Chemical compound NC1=NC(C=2N=CC=CC=2)=NC=C1C1=CC=CC=C1 BGCZFXZLBAWKGX-UHFFFAOYSA-N 0.000 title 1
- 241000233866 Fungi Species 0.000 title 1
- 230000001473 noxious effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 150000002431 hydrogen Chemical class 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- -1 nitro, amino, mercapto Chemical class 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000006193 alkinyl group Chemical group 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 abstract 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000001580 cycloalkinyl group Chemical group 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000003104 hexanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000006518 morpholino carbonyl group Chemical group [H]C1([H])OC([H])([H])C([H])([H])N(C(*)=O)C1([H])[H] 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10207428 | 2002-02-21 | ||
| DE10207428.3 | 2002-02-21 | ||
| DE10210136.1 | 2002-03-08 | ||
| DE2002110136 DE10210136A1 (de) | 2002-03-08 | 2002-03-08 | 2-(2-Pyridyl)-5-phanyl-6-aminopyrimidine, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Schadpilzen |
| PCT/EP2003/001162 WO2003070721A1 (de) | 2002-02-21 | 2003-02-06 | 2-(2-pyridyl)-5-phenyl-6-aminopyrimidine, verfahren und zwischenprodukte zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2003210217A1 true AU2003210217A1 (en) | 2003-09-09 |
Family
ID=27758401
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2003210217A Abandoned AU2003210217A1 (en) | 2002-02-21 | 2003-02-06 | 2-(2-pyridyl)-5-phenyl-6-aminopyrimidine, method and intermediate products for the production and use thereof for combating noxious fungi |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7320975B2 (enExample) |
| EP (1) | EP1504001B1 (enExample) |
| JP (1) | JP2005523286A (enExample) |
| AT (1) | ATE428705T1 (enExample) |
| AU (1) | AU2003210217A1 (enExample) |
| DE (1) | DE50311420D1 (enExample) |
| WO (1) | WO2003070721A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2006107578A (ru) | 2003-09-24 | 2007-10-27 | Вайет Холдингз Корпорейшн (Us) | 6-арилпиримидин, применяемый в качестве противоракового агента |
| BRPI0402260B1 (pt) * | 2004-06-15 | 2015-02-18 | Botica Com Farmaceutica Ltda | Composição para produtos de higiene, cosméticos e perfumes. |
| US20080132522A1 (en) * | 2004-07-14 | 2008-06-05 | Basf Aktiengesellschaft | 2-Substituted Pyrimidines, Method for Their Production and Their Use for Controlling Pathogenic Fungi |
| TW200637556A (en) * | 2005-01-31 | 2006-11-01 | Basf Ag | Substituted 5-phenyl pyrimidines I in therapy |
| US20090069180A1 (en) * | 2006-02-15 | 2009-03-12 | Joachim Rheinheimer | 2-substituted pyrimidine derivatives |
| CA2645779A1 (en) * | 2006-03-27 | 2007-10-04 | Basf Se | Substituted 5-hetaryl-4-aminopyrimidines |
| CL2007002231A1 (es) * | 2006-08-02 | 2008-04-11 | Basf Ag | Uso de compuestos derivados de 5-(het) arilpirimidina para combatir hongos daninos; compuestos derivados de 5-(het) arilpirimidina; agente fungicida; y agente farmaceutico. |
| AU2009282567B2 (en) * | 2008-08-20 | 2014-10-02 | Merck Sharp & Dohme Corp. | Substituted pyridine and pyrimidine derivatives and their use in treating viral infections |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3922735A1 (de) * | 1989-07-11 | 1991-01-24 | Hoechst Ag | Aminopyrimidin-derivate, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als fungizide |
-
2003
- 2003-02-06 US US10/505,146 patent/US7320975B2/en not_active Expired - Fee Related
- 2003-02-06 AU AU2003210217A patent/AU2003210217A1/en not_active Abandoned
- 2003-02-06 EP EP03742510A patent/EP1504001B1/de not_active Expired - Lifetime
- 2003-02-06 AT AT03742510T patent/ATE428705T1/de not_active IP Right Cessation
- 2003-02-06 DE DE50311420T patent/DE50311420D1/de not_active Expired - Lifetime
- 2003-02-06 JP JP2003569628A patent/JP2005523286A/ja active Pending
- 2003-02-06 WO PCT/EP2003/001162 patent/WO2003070721A1/de not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| US20050107401A1 (en) | 2005-05-19 |
| US7320975B2 (en) | 2008-01-22 |
| EP1504001B1 (de) | 2009-04-15 |
| EP1504001A1 (de) | 2005-02-09 |
| DE50311420D1 (de) | 2009-05-28 |
| ATE428705T1 (de) | 2009-05-15 |
| WO2003070721A1 (de) | 2003-08-28 |
| JP2005523286A (ja) | 2005-08-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK6 | Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase |