首页> 外国专利> New pyrazine compounds useful in the fungicidal agent, for combating plant pathogenic fungus in protecting materials, plants, ground or seeds and to treat cancer

New pyrazine compounds useful in the fungicidal agent, for combating plant pathogenic fungus in protecting materials, plants, ground or seeds and to treat cancer

机译:可用于杀真菌剂的新型吡嗪化合物,可用于对抗植物病原真菌,保护材料,植物,地面或种子并治疗癌症

摘要

Pyrazine compounds (I) and their salts are new. Pyrazine compounds of formula (I) and their salts are new. R1, R4halo (preferred), CN, 1-8C alkoxy or phenyl-1-4C alkyl; R21-12C alkyl, 1-10C haloalkyl, 2-10C alkenyl, 2-10C haloalkenyl, 2-10C alkynyl, 2-10C haloalkynyl, 3-6C cycloalkyl, 3-8C cycloalkenyl, 3-12C cycloalkenyl, 3-6C halocycloalkyl, 3-12C halocycloalkenyl, aryl (preferred) or aromatic heterocycle (containing 1-4 R1a group and other than carbon atoms, up to 4 N or 0-2 N, S or O as a ring atoms, where the aromatic groups are 5-10 membered ring system); R1a : CN, nitro, OH, carboxyl, 1-6C alkyl, 2-6C alkynyl, 3-6C cycloalkyl, 3-8C cycloalkenyl, 1-6C alkoxy, 2-6C alkenyloxy, 3-6C alkynyloxy, 3-6C cycloalkoxy, 3-6C cycloalkenyloxy, C(O)R1n, C(O)OR1n, C(S)OR1n, C(O)SR1n, C(S)SR, OC(O)OR1n, 1-6C alkylthio, amino, 1-6C alkylamino, di-1-6C alkylamino, 1-6C alkylene, oxy-1-4C alkylene, oxy-1-3C alkylenoxy, where the divalent groups are bonded to the same atom or at the adjacent atoms, phenyl, naphthyl, 5-10 membered saturated, partially unsaturated or aromatic heterocycle (containing other than the carbon atoms, an up to 4 N or up to 3 N, S or O as a ring atom); R1n : 1-8C alkyl, 3-8C alkenyl, 3-8C alkynyl, 3-6C cycloalkyl or 3-6C cycloalkenyl, where the aliphatic, alicyclic or aromatic groups in R1a and R1n are halogenated partially or completely and carries 1-3 groups of R1b; R1b : halo, CN, nitro, OH, mercapto, amino, carboxyl, alkyl, haloalkyl, alkenyl, alkoxy, haloalkoxy, alkenyloxy, alkynyloxy, alkylthio, alkylamino, dialkylamino, formyl, alkylcarbonyl, alkylsulfonyl, alkylsulfoxyl, alkoxycarbonyl, alkylcarbonyloxy, alkoxycarbonyloxy, aminocarbonyl, aminothiocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, where the alkyl group contains 1-6 carbon atom and the alkenyl- or alkynyl group contains 2-8 carbon atoms, cycloalkyl, cycloalkoxy, heterocyclyl, heterocyclyloxy, where the cyclic system contains 3-10 ring member, aryl, aryloxy, arylthio, aryl-1-6C alkoxy, aryl-1-6C alkyl, hetaryl, hetaryloxy, hetarylthio, where the aryl residue is preferably 6-10 ring members containing 5-6 membered hetaryl residues, where the cyclic systems are partially or completely halogenated and/or substituted by alkyl- or haloalkyl group; R3aryl (preferred) or heteroaryl, containing other than carbon atom, up to 4 N or 0-2 N, S or as a ring atom, where the group is 5-10 membered ring system, containing a group L1 in ortho position to the bonding to the pyridazine-basic unit and at least a further group Lm; L1halo, 1-4C alkyl, 1-4C haloalkyl; L : halo, OH, OCN, CN, nitro, 1-8C alkyl, 1-8C haloalkyl, 2-10C alkenyl, 2-10C haloalkenyl, 2-10C alkynyl, 3-6C cycloalkyl, 3-6C halocycloalkyl, 3-6C cycloalkenyl, 1-8C alkoxy, 1-8C haloalkoxy, 2-10C alkenyloxy, 2-10C alkynyloxy, 3-6C cycloalkyloxy, 3-6C cycloalkenyloxy, amino, 1-4C alkylamino, di-(1-4C)-alkylamino, C(O)-R1z, C(S)-R1z, S(O)n-R1z, 1-8C alkoxyimino- (1-8C)-alkyl, 2-10C alkenyloxyimino-(1-8C)-alkyl, 2-10C alkynyloxyimino-(1-8C)-alkyl, 2-10C alkynylcarbonyl, 3-6C cycloalkylcarbonyl, or 5-10 membered saturated, partially unsaturated or aromatic heterocyclic containing 1-4 heteroatoms of O, N or S; R1z : H, 1-4C alkyl, 1-2C haloalkyl, 1-4C alkoxy, 2-4C alkenyloxy, 2-4C alkynyloxy, where the group R1z is substituted with 1-3 R1b group; n : 0-2; and m : 1-4. Independent claims are included for: (1) the preparation of (I); (2) 1,2-dihydro-pyridazine-3,6-dione compound of formula (II); a fungicidal agent containing a solid or liquid carrier and (I); and (3) a seed containing (I) in a quantity of 1-1000 g/100 kg. [Image] [Image] ACTIVITY : Fungicide; Cytostatic. MECHANISM OF ACTION : None given.
机译:吡嗪化合物(I)及其盐是新的。式(I)的吡嗪化合物及其盐是新的。 R1>,R4>卤代(优选),CN,1-8C烷氧基或苯基-1-4C烷基; R2> 1-12C烷基,1-10C卤代烷基,2-10C烯基,2-10C卤代烯基,2-10C炔基,2-10C卤代炔基,3-6C环烷基,3-8C环烯基,3-12C环烯基,3-6C卤代环烷基,3-12C卤代环烯基,芳基(优选)或芳族杂环(含有1-4个R1a基团且除碳原子外,最多4 N或0-2 N,S或O为环原子,其中芳族基团为5-10元环系统); R1a:CN,硝基,OH,羧基,1-6C烷基,2-6C炔基,3-6C环烷基,3-8C环烯基,1-6C烷氧基,2-6C烯基氧基,3-6C炔基氧基,3-6C环烷氧基, 3-6C环烯氧基,C(O)R1n,C(O)OR1n,C(S)OR1n,C(O)SR1n,C(S)SR,OC(O)OR1n,1-6C烷硫基,氨基,1- 6C烷基氨基,二1-6C烷基氨基,1-6C亚烷基,氧基1-4C亚烷基,氧基1-3C亚烷基氧基,其中二价基团与相同原子或相邻原子键合,苯基,萘基5 -10元饱和,部分不饱和或芳族杂环(除碳原子外,最多4 N或最多3 N,S或O为环原子); R1n:1-8C烷基,3-8C烯基,3-8C炔基,3-6C环烷基或3-6C环烯基,其中R1a和R1n中的脂族,脂环族或芳族基团被部分或全部卤化并带有1-3个基团R1b; R 1b:卤素,CN,硝基,OH,巯基,氨基,羧基,烷基,卤代烷基,烯基,烷氧基,卤代烷氧基,烯基氧基,炔基氧基,烷硫基,烷基氨基,二烷基氨基,甲酰基,烷基羰基,烷基磺酰基,烷基亚磺酰基,烷氧基羰基,烷基羰氧基,烷氧基羰基氨基羰基,氨基硫羰基,烷基氨基羰基,二烷基氨基羰基,烷基氨基硫羰基,二烷基氨基硫羰基,其中烷基含有1-6个碳原子,烯基或炔基含有2-8个碳原子,环烷基,环烷氧基,杂环基,杂环基氧基,其中环系统含有3 -10个环成员,芳基,芳氧基,芳硫基,芳基-1-6C烷氧基,芳基-1-6C烷基,杂芳基,杂芳氧基,杂芳硫基,其中芳基优选为6-10个含5-6元杂芳基残基的环成员,当环状系统部分或完全被烷基或卤代烷基卤化和/或取代时; R 3>芳基(优选)或杂芳基,其含有除碳原子以外的至多4 N或0-2 N,S或作为环原子,其中该基团是5-10元环系统,在邻位含有基团L1>与哒嗪碱性单元和至少另一个基团Lm结合的位置; L1>卤代,1-4C烷基,1-4C卤代烷基; L:卤素,OH,OCN,CN,硝基,1-8C烷基,1-8C卤代烷基,2-10C烯基,2-10C卤代烯基,2-10C炔基,3-6C环烷基,3-6C卤代环烷基,3-6C环烯基,1-8C烷氧基,1-8C卤代烷氧基,2-10C烯氧基,2-10C炔氧基,3-6C环烷氧基,3-6C环烯氧基,氨基,1-4C烷基氨基,二(1-4C)-烷基氨基,C (O)-R1z,C(S)-R1z,S(O)n-R1z,1-8C烷氧基亚氨基-(1-8C)-烷基,2-10C烯基氧基亚氨基-(1-8C)-烷基,2-10C炔基氧基亚氨基-(1-8C)-烷基,2-10C炔基羰基,3-6C环烷基羰基或5-10元饱和的,部分不饱和的或芳族的杂环,含1-4个O,N或S杂原子; R1z:H,1-4C烷基,1-2C卤代烷基,1-4C烷氧基,2-4C烯基氧基,2-4C炔基氧基,其中R1z基团被1-3个R1b基团取代; n:0-2;和m:1-4。独立索赔包括:(1)(I)的制备; (2)式(II)的1,2-二氢哒嗪-3,6-二酮化合物;含有固体或液体载体和(I)的杀真菌剂; (3)含有(I)的1-1000g / 100kg种子。 [图片] [图片]活动:杀菌剂;止细胞的。作用机理:未给出。

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