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1. 发明公开

KR1020050119172A 7-알케닐아미노-트리아졸로피리미딘, 그의 제조 방법 및유해 진균류를 방제하기 위한 그의 용도와 상기트리아졸로피리미딘을 함유하는 물질 无效
标题翻译： 7-烯丙基氨基三唑并嘧啶，其生产方法及其用于控制有害真菌的物质及含有三唑并嘧啶的物质
公开(公告)号：KR1020050119172A
公开(公告)日：2005-12-20
申请号：KR1020057018523
申请日：2004-03-24
申请人： 바스프 에스이
发明人： 토르모이블라스코,조르디 , 블레트너,카르슈텐 , 뮐러,베른트 , 게베르,마르쿠스 , 그람메노스,바실리오스 , 그로테,토마스 , 기프서,안드레아스 , 라인하이머,요아힘 , 쉐퍼,페터 , 쉬벡,프랑크 , 쉬뵈글러,안야 , 쉬에러,마리아 , 슈트라트만,지그프리트 , 쇠플,울리히 , 슈틸,라인하르트
IPC分类号： C07D487/04
CPC分类号： C07D487/04 , A01N43/90
摘要： The invention relates to 7-alkenylamino- triazolopyrimidines of formula (I) wherein the substituents have the following meaning: L represents halogen, alkyl, halogenalkyl, alkoxy, amino, NHR or NR2; R represents alkyl or alkyl-carbonyl; m represents 1, 2, 3, 4 or 5; X represents halogen, cyano, alkyl, halogenalkyl or alkoxy; R1 represents alkyl or halogenalkyl; R2represents hydrogen, alkyl or halogenalkyl; R3 represents alkenyl which is unsubstituted or partially or totally halogenated or can be substituted according to the description; R 4 represents hydrogen or alkyl, R3 and R4 can form, together with the nitrogen atom whereon they are bound, a five or six- membered unsaturated ring which can be interrupted by an atom from the groups O, N and S and/or can include one or several substituents. The invention also relates to methods for producing said compounds, agents containing said compounds and the use thereof in controlling plant pathogenic harmful fungi.
摘要翻译：本发明涉及式（I）的7-烯基氨基 - 三唑并嘧啶，其中取代基具有下列含义：L代表卤素，烷基，卤代烷基，烷氧基，氨基，NHR或NR2; R代表烷基或烷基 - 羰基; m表示1,2,3,4或5; X表示卤素，氰基，烷基，卤代烷基或烷氧基; R1代表烷基或卤代烷基; R2代表氢，烷基或卤代烷基; R3表示根据描述未被取代或部分或完全卤化或可被取代的烯基; R 4表示氢或烷基，R 3和R 4可以与它们所连接的氮原子一起形成可以被O，N和S基团的原子中间的五或六元不饱和环和/或可以包括一个或几个取代基。本发明还涉及生产所述化合物的方法，含有所述化合物的试剂及其在控制植物病原性有害真菌中的用途。

2. 发明授权

KR100758318B1 트리아졸로피리미딘 유도체를 기재로 한 살진균성 혼합물 失效
标题翻译：基于三唑并嘧啶衍生物的杀真菌剂
公开(公告)号：KR100758318B1
公开(公告)日：2007-09-13
申请号：KR1020057024262
申请日：2004-06-08
申请人： 바스프 에스이
发明人： 토르모이블라스코,조르디 , 그로테,토마스 , 쉐러,마리아 , 스티를,라인하르트 , 스트라트만,지그프리트 , 쇠플,울리히
IPC分类号： A01N43/90 , A01P13/00
CPC分类号： A01N43/90 , A01N43/54 , A01N2300/00
摘要： 본 발명은 활성 성분으로서, (1) 하기 화학식 I의 트리아졸로피리미딘 유도체 및 (2) 하기 화학식 Ⅱ의 피리미딘아닐리드를 상승작용적 유효량으로 포함하는 살진균성 혼합물에 관한 것이다.

상기 식에서, R은 메틸, 시클로프로필 또는 1-프로피닐이다.
본 발명은 또한 화학식 I의 화합물 및 화학식 II의 화합물들중 하나의 혼합물을 사용하여 난균(
Oomycetes ) 강에 속하는 유해 진균류를 방제하는 방법, 및 상기 혼합물을 함유하는 제제 이외에 이러한 유형의 혼합물을 제조하기 위한 화학식 I의 화합물 및 화학식 II의 화합물들중 하나의 용도에 관한 것이다.
트리아졸로피리미딘 유도체, 피리미딘아닐리드, 난균류, 진균류의 방제 방 법, 살진균성 혼합물

3. 发明公开

KR1020070104516A 6-페닐-7-아미노-트리아졸로피리미딘, 이의 제조 방법,병원성 진균을 방제하기 위한 상기 화합물의 용도, 및 상기화합물을 포함하는 제제 无效
标题翻译： 6-苯基-7-氨基三唑并嘧啶，其生产方法，其用于控制致病真菌的用途，以及含有它们的药剂
公开(公告)号：KR1020070104516A
公开(公告)日：2007-10-26
申请号：KR1020077007910
申请日：2005-09-02
申请人： 바스프 에스이
发明人： 블레트너,카르스텐 , 토르모이블라스코,조르디 , 뮐러,베른트 , 게베어,마르쿠스 , 그래메노스,와실리오스 , 그로테,토마스 , 휜저,유도 , 라인하이머,요아킴 , 샤퍼,페테르 , 쉬베크,프랑크 , 슈뵈글러,안야 , 디츠,요켄 , 스피크맨,존-브라이언 , 얍스,토르스텐 , 스트라트만,지그프리트 , 셰플,울리히 , 셰어러,마리아 , 스티얼,라인하르트
IPC分类号： C07D487/04 , A01N43/90
CPC分类号： A01N43/90 , A01N47/06 , A01N47/12 , A01N47/16 , C07D487/04
摘要： The invention relates to 6-phenyl-7-amino-triazolopyrimidines of formula (I), wherein the substituents have the following designations: R1 represents hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, halogencycloalkenyl, alkinyl, halogenalkinyl or phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heteroycle, containing between one and four heteroatoms from the group containing O, N or S; R2 represents alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, halogencycloalkenyl, alkinyl, halogenalkinyl or phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heterocycle, containing between one and four heteroatoms from the group containing O, N or S; R3,R4,R5, R6,R7 represent hydrogen or one of the groups cited for R2, R4 also being able to form a five-membered or six-membered saturated or unsaturated ring with R3 or R 6, that can contain, in addition to carbon atoms and as a ring member, between one and three other heteroatoms from the group containing O, N and S; R2 and R3, R4 and R 5, and R6 and R7 can respectively form, in order to form spiro groups, a C2-C5 alkylene, alkenylene, or alkinylene chain, which can be broken by between one and three heteroatoms from the group containing O, N and S; p represents 0 or 1; L represents halogen, alkyl, halogenalkyl, alkoxy, cyano, nitro, amino, alkylamino, dialkylamino, alkylcarbonylamino, C(O)-R, S(O)n-R; where n represents 0, 1 or 2; R represents hydrogen, alkyl, halogenalkyl, alkoxy, alkenyloxy, alkinyloxy, amino, alkylamino, dialkylamino; m represents 1, 2, 3, 4 or 5; X represents halogen, cyano, alkyl, alkoxy, alkenyloxy, alkinyloxy or halogenalkoxy, Y represents oxygen or sulphur; Z represents hydrogen, alkyl, halogenalkyl, cycloalkyl, alkylcarbonyl, cycloalkylcarbonyl, alkenyl, halogenalkenyl, cycloalkenyl, alkinyl, halogenalkinyl, phenyl, naphthyl, a five-membered to ten-membered saturated, partially unsaturated or aromatic heterocycle, containing between one and four heteroatoms from the group containing O, N and S; or Z can also form, with R4 or R6, a five-membered or six-membered ring that can contain, in addition to carbon atoms and Y, one or two other heteroatoms from the group containing O, N and S, as a ring member; the groups R1 to R7, Z and R being able to be substituted according to the description. The invention also relates to methods for producing said compounds, to agents containing the same, and to the use thereof for controlling plant pathogenic fungi.
摘要翻译：本发明涉及式（I）的6-苯基-7-氨基 - 三唑并嘧啶，其中取代基具有以下指定：R 1表示氢，烷基，卤代烷基，环烷基，卤代烷基，烯基，卤素链烯基，环烯基，卤代烯基，炔基，卤代羰基或苯基，萘基或五元或六元饱和，部分不饱和或芳族杂环，含有一个至四个含有O，N或S的基团的杂原子; R 2代表烷基，卤素烷基，环烷基，卤代烷基，链烯基，卤代烯基，环烯基，卤代烯基，炔基，卤代炔基或苯基，萘基或五元或六元饱和的部分不饱和或芳族杂环，含有O，N或S的基团; R 3，R 4，R 5，R 6，R 7表示氢或R 2所列的基团之一，R4还能够与R 3或R 6形成五元或六元饱和或不饱和的环，碳原子和作为环成员，来自含有O，N和S的基团的一个和三个其它杂原子; R2和R3，R4和R5以及R6和R7可以分别形成C2-C5亚烷基，亚烯基或亚链烯基链，以形成螺环，其可以由含有 O，N和S; p表示0或1; 烷氧基，氰基，硝基，氨基，烷基氨基，二烷基氨基，烷基羰基氨基，C（O）-R，S（O）n -R; 其中n表示0,1或2; R代表氢，烷基，卤代烷基，烷氧基，烯氧基，烷氧基，氨基，烷基氨基，二烷基氨基; m表示1,2,3,4或5; X表示卤素，氰基，烷基，烷氧基，烯氧基，烷氧基或卤代烷氧基，Y表示氧或硫; Z代表氢，烷基，卤代烷基，环烷基，烷基羰基，环烷基羰基，烯基，卤代烯基，环烯基，炔基，卤代炔基，苯基，萘基，含有一个和四个杂原子的五元至十元饱和，部分不饱和或芳族杂环来自含有O，N和S的基团; 或Z也可以与R4或R6形成五元或六元环，除了碳原子和Y之外，还可以含有一个或两个其它含有O，N和S的基团的杂原子作为环会员; 根据说明可以使R1〜R7，Z，R基团取代。本发明还涉及生产所述化合物，含有该化合物的药剂的方法及其用于防治植物致病真菌的方法。

4. 发明公开

KR1020060088568A 쌀 병원균 방제용 살진균성 혼합물 无效
标题翻译：用于控制稻米病虫害的防菌混合物
公开(公告)号：KR1020060088568A
公开(公告)日：2006-08-04
申请号：KR1020067010329
申请日：2004-11-18
申请人： 바스프 에스이
发明人： 토르모이블라스코,조르디 , 그로테,토마스 , 쉐러,마리아 , 스티얼,라인하르트 , 스트라스만,지그프리드 , 쉐플,울리히
IPC分类号： A01N43/90 , A01P3/00
CPC分类号： A01N43/90 , A01N47/14 , A01N2300/00
摘要： The invention relates to fungicidal mixtures for controlling rice pathogens, which comprise as the active components: 1) the triazolopyrimidine derivative of formula (I), and 2) a dithiocarbamate II selected from the group including manganese ethylenebis(dithiocarbamate) zinc complex (II.1), manganese ethylenebis(dithiocarbamate) (II.2), zinc ammoniate ethylenebis(dithiocarbamate) (II.3), zinc ethylenebis(dithiocarbamate) (II.4) and bis(dimethylthiocarbamoyl)disulfide (II.5) in a synergistically effective amount. The invention also relates to methods for controlling rice pathogens with mixtures of compound I with the compounds II and to the use of compound I with the compounds II for producing the aforementioned mixtures, and to agents that contain said mixtures.
摘要翻译：本发明涉及用于控制水稻病原体的杀真菌混合物，其包含作为活性组分的：1）式（I）的三氮代嘧啶衍生物，和2）选自亚乙基双（二硫代氨基甲酸）锌络合物（II）的二硫代氨基甲酸酯II。 1），亚硫酸亚乙基酯（II.2），亚氨基亚乙基双（二硫代氨基甲酸）锌（II.3），亚乙基双（二硫代氨基甲酸）亚乙酯（II.4））和双（二甲基硫代氨基甲酰基）二硫化物（II.5）有效量。本发明还涉及使用化合物I与化合物II的混合物来控制水稻病原体的方法，以及化合物I与化合物II在制备上述混合物中的用途，以及含有所述混合物的试剂。

5. 发明公开

KR1020050115925A 트리플루오로메틸-티오펜 카르복실산 아닐리드 및 그의항진균제로서의 용도 无效
标题翻译：三氟甲基硫代羧酸类抗坏血酸及其作为杀真菌剂的用途
公开(公告)号：KR1020050115925A
公开(公告)日：2005-12-08
申请号：KR1020057017804
申请日：2004-03-20
申请人： 바스프 에스이
发明人： 게베르,마르쿠스 , 뮬러,벤드 , 그로테,토마스 , 그라메노스,바실리오스 , 기프제르,안드레아스 , 토르모이블라스코,조르디 , 쉬베글러,안자 , 레인하이머,조아킴 , 블레트너,칼스텐 , 쉬베크,프랑크 , 라크,미카엘 , 쇼플,울리치 , 스트라트만,시그프리드 , 스티를라인하드 , 레테,잔
IPC分类号： C07D333/38 , C07D333/20 , C07D333/12
CPC分类号： C07D333/38
摘要： The invention relates to trifluoromethyl- thiophene carboxylic acid anilides of general formulas I, II, and III, wherein the substituents have the following meaning: R1, R 4 independently represent C1-C4alkyl, C3- C6 cycloalkyl, C2-C4 alkenyl, C2-C4 alkinyl, C1-C4 alkoxy, said groups being optionally substituted by halogen, H, halogen, nitro, CN; R2 represents H, OH, C1-C4 alkyl, C 3-C6 cycloalkyl, C1-C4 alkoxy, said groups being optionally substituted by halogen; R3represents C1-C12 alkyl, C3-C12 cycloalkyl, C2-C12 alkenyl, C5-C12 cycloalkenyl, C2-C12 alkinyl, C3-C12 cycloalkyl-C1-C4 alkyl, said groups being optionally substituted by R7; phenyl, phenyl-C1-C6 alkyl, phenyl-C2-C6 alkenyl, phenyl-C2-C 6 alkinyl, phenyloxy-C1-C6 alkyl, phenyloxy-C2- C6 alkenyl, phenyloxy-C2-C6 alkinyl, the alkyl portion, alkenyl portion, and alkinyl portion being optionally substituted by R 7 and the phenyl ring being optionally substituted by R5; -C(R8)=NOR6; X represents O, S, or a direct bond; R5 represents H, C1-C4alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C2-C4 alkenyl, C2-C4 alkinyl, said groups being optionally substituted by halogen, halogen, nitro, CN, phenyl which can be substituted by R1, phenoxy that can be substituted by R1, C1-C6 alkyl-phenyl, the alkyl portion being optionally substituted by halogen and the phenyl ring being optionally substituted by R1; R6 represents C 1-C4 alkyl, C3-C6 cycloalkyl, C2-C4 alkenyl, C2-C4 alkinyl, said groups being optionally substituted by halogen, phenyl which can be substituted by R1; R7 represents C 1-C4 alkyl, C1-C8 alkoxy, C2-C8 alkenyloxy, C2-C8 alkinyloxy, C1-C4 alkoxy-C 1-C8 alkoxy, said groups being optionally substituted by halogen, halogen; R8 represents H, R7, or C1-C12 alkyl, C3- C12 cycloalkyl, C2-C12 alkenyl, C5-C12 cycloalkenyl, C3-C12 cycloalkyl-C1-C4 alkyl, said groups being optionally substituted by halogen; phenyl which can be substituted by R5; n represents 0 to 4; and m represents 0, 1. Also disclosed is the use of the inventive trifluoromethyl- thiophene carboxylic acid anilides as fungicides and agents containing said trifluoromethyl-thiophene carboxylic acid anilides.
摘要翻译：本发明涉及通式I，II和III的三氟甲基噻吩羧酸酰胺，其中取代基具有以下含义：R 1，R 4独立地表示C 1 -C 4烷基，C 3 -C 6环烷基，C 2 -C 4烯基， C4烷氧基，C1-C4烷氧基，所述基团任选被卤素，H，卤素，硝基，CN取代; R 2表示H，OH，C 1 -C 4烷基，C 3 -C 6环烷基，C 1 -C 4烷氧基，所述基团任选被卤素取代; R3代表C 1 -C 12烷基，C 3 -C 12环烷基，C 2 -C 12烯基，C 5 -C 12环烯基，C 2 -C 12炔基，C 3 -C 12环烷基-C 1 -C 4烷基，所述基团任选被R 7取代; 苯基-C 1 -C 6烷基，苯基-C 2 -C 6烯基，苯基-C 2 -C 6炔基，苯氧基-C 1 -C 6烷基，苯氧基-C 2 -C 6烯基，苯氧基-C 2 -C 6炔基，烷基部分，链烯基部分和炔基部分任选被R 7取代，并且苯环任选被R 5取代; -C（R8）= NOR6; X表示O，S或直接键; R5表示H，C1-C4烷基，C3-C6环烷基，C1-C4烷氧基，C2-C4烯基，C2-C4炔基，所述基团任选被卤素，卤素，硝基，CN取代，可被R 1取代的苯基，可被R 1，C 1 -C 6烷基 - 苯基取代的苯氧基，烷基部分任选被卤素取代，苯环任选被R 1取代; R 6表示C 1 -C 4烷基，C 3 -C 6环烷基，C 2 -C 4烯基，C 2 -C 4炔基，所述基团任选被卤素取代，可被R 1取代的苯基; R 7表示C 1 -C 4烷基，C 1 -C 8烷氧基，C 2 -C 8烯氧基，C 2 -C 8烷氧基，C 1 -C 4烷氧基-C 1 -C 8烷氧基，所述基团任选被卤素，卤素取代; R8表示H，R7或C1-C12烷基，C3-C12环烷基，C2-C12链烯基，C5-C12环烯基，C3-C12环烷基-C1-C4烷基，所述基团任选被卤素取代; 可被R5取代的苯基; n表示0〜4; 并且m表示0。还公开了本发明的三氟甲基 - 噻吩羧酸二酰胺作为杀真菌剂和含有所述三氟甲基 - 噻吩羧酸苯胺的试剂的用途。

6. 发明公开

KR1020070024646A 트리아졸로피리미딘 화합물 및 그의 병원성 진균류 방제를위한 용도 无效
标题翻译：三唑并嘧啶化合物及其用于控制致病真菌的用途
公开(公告)号：KR1020070024646A
公开(公告)日：2007-03-02
申请号：KR1020067027269
申请日：2005-06-24
申请人： 바스프 에스이
发明人： 블레트너,카르스텐 , 쉬베크,프랑크 , 토르모이블라스코,조르디 , 뭴러,베른트 , 게베허,마르쿠스 , 그람메노스,와실리오스 , 그로테,토마스 , 라인하이머,요아킴 , 섀퍼,페터 , 슈뵈글러,아냐 , 바그너,올리버 , 스피크만,존-브라이언 , 얍스,토르스텐 , 스트라트만,지그프리드 , 슈외플,울리히 , 쉐러,마리아 , 스티얼,라인하르트
IPC分类号： C07D487/04 , A01N43/90
CPC分类号： A01N43/90 , C07D487/04
摘要： The invention relates to novel triazolopyrimidine compounds of general formula (I) wherein: X represents halogen, cyano, C1-C4 alkyl, C1-C4 alkyl halide, C1-C4 alkoxy or C1-C2 alkoxy halide; W represents oxygen or sulfur; Y represents O-R4 or a group NR5R6; A represents a chemical bond or a group CR7R8, and; variables L, R1 to R7 have the definitions cited in Claim 1. The invention also relates to the use of the triazolopyrimidine compounds of general formula (I), their tautomers and their agriculturally compatible salts for controlling plant-pathogenic fungi, and to a method for controlling plant-pathogenic fungi, which is characterized in that the fungi or the materials, plants, soil or seeds to be protected from fungal attack are treated with an effective amount of a compound of general formula (I), a tautomer (I) and/or with an agriculturally compatible salt of (I) or of the tautomer thereof. ® KIPO & WIPO 2007
摘要翻译：本发明涉及通式（I）的新型三唑并嘧啶化合物，其中：X表示卤素，氰基，C 1 -C 4烷基，C 1 -C 4烷基卤，C 1 -C 4烷氧基或C 1 -C 2烷氧基卤化物; W表示氧或硫; Y表示O-R4或NR5R6基团; A表示化学键或CR7R8基团，变体L，R 1至R 7具有权利要求1中引用的定义。本发明还涉及通式（I）的三唑并嘧啶化合物，其互变异构体及其农业上相容的盐用于控制植物致病性真菌的用途，以及方法用于控制植物致病性真菌，其特征在于用有效量的通式（I）的化合物，互变异构体（I））的化合物处理要保护免受真菌侵袭的真菌或物质，植物，土壤或种子，和/或与（I）的农业相容的盐或其互变异构体的盐。 ®KIPO＆WIPO 2007

7. 发明公开

KR1020060015652A 트리아졸로피리미딘 유도체를 기재로 한 살진균성 혼합물 失效
标题翻译：基于三唑并嘧啶衍生物的杀真菌剂
公开(公告)号：KR1020060015652A
公开(公告)日：2006-02-17
申请号：KR1020057024262
申请日：2004-06-08
申请人： 바스프 에스이
发明人： 토르모이블라스코,조르디 , 그로테,토마스 , 쉐러,마리아 , 스티를,라인하르트 , 스트라트만,지그프리트 , 쇠플,울리히
IPC分类号： A01N43/90 , A01P13/00
CPC分类号： A01N43/90 , A01N43/54 , A01N2300/00
摘要： The invention relates to fungicidal mixtures, containing the following active components: 1) a triazolopyrimidine derivative of formula (I); and 2) a pyrimidine anilide of formula (II), in which R represents methyl, cyclopropyl or 1-propinyl in a synergistically effective quantity. The invention also relates to methods for combating harmful fungi in the class of Oomycetes using a mixture of compound (I) and one of the compounds (II) and to the use of compound (I) and one of the compounds (II) for producing mixtures of this type, in addition to agents containing said mixtures.
摘要翻译：本发明涉及含有以下活性组分的杀真菌混合物：1）式（I）的三唑并嘧啶衍生物; 和2）式（II）的嘧啶酰苯胺，其中R表示协同有效量的甲基，环丙基或1-丙炔基。本发明还涉及使用化合物（I）和化合物（II）之一的混合物以及使用化合物（I）和化合物（II）之一来制备卵菌纲中的有害真菌的方法除了含有所述混合物的试剂之外，还有这种混合物。

8. 发明公开

KR1020050111627A 7-알키닐아미노-트리아졸로피리미딘, 그의 제조 방법 및유해 진균류를 박멸하기 위한 그의 용도 및 상기 화합물을함유하는 작용제 无效
标题翻译： 7-烷基氨基三唑并嘧啶，其生产方法及其用途，用于混合有害真菌和含有化合物的试剂
公开(公告)号：KR1020050111627A
公开(公告)日：2005-11-25
申请号：KR1020057018621
申请日：2004-03-30
申请人： 바스프 에스이
发明人： 토르모이블라스코,조르디 , 블레트너,카르슈텐 , 뮐러,베른트 , 게베르,마르쿠스 , 그람메노스,바실리오스 , 그로테,토마스 , 기프서,안드레아스 , 라인하이머,요아힘 , 쉐퍼,페터 , 쉬벡,프랑크 , 쉬뵈글러,안야 , 쉬에러,마리아 , 슈트라트만,지그프리트 , 쇠플,울리히 , 슈틸,라인하르트
IPC分类号： C07D487/04
CPC分类号： C07D487/04 , A01N43/90
摘要： 7-alkinylamino-triazolopyrimidins of formula (I), wherein the substituents have the following meanings: L = halogen, alkyl, halogenalkyl, alkoxy, amino, NHR, NR2, cyano, S(O)nA1 or C(O)A2; R = alkyl or alkylcarbonyl; A1 = hydrogen, hydroxy, alkyl, alkylamino or aialkylamino; n = 0, 1 or 2; A2 = alkenyl, alkoxy, halogenalkoxy or one of the groups cited in A1; m = 1, 2, 3, 4 or 5, whereby at least one group L is present in an ortho-position to the bond with the triazolopyrimidine skeleton; X = halogen, cyano, alkyl, halogenalkyl or alkoxy; R1 = hydrogen or alkyl; R2 = alkinyl which can be unsubstituted or substituted according to the description. The invention also relates to methods for the production of said compounds, agents containing said compounds and the use thereof to combat harmful phytopathogenic fungi.
摘要翻译：式（I）的7-烷基氨基 - 三唑并嘧啶类，其中取代基具有以下含义：L =卤素，烷基，卤代烷基，烷氧基，氨基，NHR，NR2，氰基，S（O）nA1或C（O） R =烷基或烷基羰基; A1 =氢，羟基，烷基，烷基氨基或亚烷基氨基; n = 0,1或2; A2 =烯基，烷氧基，卤代烷氧基或A1中引用的基团之一; m = 1,2,3,4或5，其中至少一个基团L存在于与三唑并嘧啶骨架的键的邻位; X =卤素，氰基，烷基，卤代烷基或烷氧基; R1 =氢或烷基; R2 =根据描述可以是未取代或取代的炔基。本发明还涉及生产所述化合物的方法，含有所述化合物的试剂及其用于对抗有害植物病原真菌的用途。

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