首页> 外国专利> A N - acetonilbenzamida Fungicide composition, a process for their PreparationA method for controlling phytopathogenic fungi and a process for preparing a racemic mixture of (R) and (S) Enantiomers of said composition

A N - acetonilbenzamida Fungicide composition, a process for their PreparationA method for controlling phytopathogenic fungi and a process for preparing a racemic mixture of (R) and (S) Enantiomers of said composition

机译:N-乙腈苯甲酰胺类杀菌剂组合物,其制备方法,控制植物病原性真菌的方法以及该组合物的(R)和(S)对映异构体的外消旋混合物的制备方法

摘要

It refers to new components, including (a) a corresponding isomer of n-acrylonitrile-benzodienyl fungicide (I),where: 1.A is selected from N and C-R5; 2. R1 and R2 are distinct and are independently selected from H, (C1-C6) alkyl, (C2-C6) alkenyl, (C2-C6) alkynyl, and halo (C1-C6) alkyl, and R2 is stereochemically larger than R1; 3. R3, R4 and R5 are independently selected from H, halo, (C1-C6) alkyl, (C2-C6) alkenyl, halo (C1-C6) alkyl, (C1-C6) alkoxy, cyano, nitro, -CR6 = NOR7, -NR8R9, -CONR10R11 and -NH-CO-OR12 where R6 is selected from H, (C1-C6) alkyl, (C2-C6) alkenyl, and (C2-C6) alkynyl; R7 is selected from H, (C1-C6) alkyl, (C2-C6) alkenyl, (C2-C6) alkynyl, and (C1-C6) alkylcarbonyl, R8 and R9 are independently selected from H, (C1-C6) alkyl ,and (C1-C6) alkylcarbonyl; R10 and R11 are independently selected from H and (C1-C6) alkyl; and R12 is selected from H, (C1-C6) alkenyl, and (C2-C6) alkynyl; and 4. X, Y, and Z are independently selected from H, halo, cyano, thiocyan, isothiocyan, and (C1-C4) alkyl sulfonyloxy, provided that X, Y, and Z are not all H; and b) an agronomically acceptable vehicle, where the composition is predominantly free of the compound of formula (I) where R1 is stereochemically longer than R2. A process for its preparation is further described,A method of controlling plant pathogenic fungi and the process of producing racemic mixtures of their corresponding isomers (R) and (s).
机译:它指的是新的组分,包括(a)正丙烯腈-苯并二烯基杀真菌剂(I)的相应异构体,其中:1.A选自N和C-R5; 2. R1和R2是截然不同的,并且分别选自H,(C1-C6)烷基,(C2-C6)烯基,(C2-C6)炔基和卤素(C1-C6)烷基,并且R2在立体化学上大于R1; 3.R 3,R 4和R 5独立地选自H,卤素,(C 1 -C 6)烷基,(C 2 -C 6)烯基,卤素(C 1 -C 6)烷基,(C 1 -C 6)烷氧基,氰基,硝基,-CR 6。 = NOR7,-NR8R9,-CONR10R11和-NH-CO-OR12,其中R6选自H,(C1-C6)烷基,(C2-C6)烯基和(C2-C6)炔基; R7选自H,(C1-C6)烷基,(C2-C6)烯基,(C2-C6)炔基和(C1-C6)烷基羰基,R8和R9独立地选自H,(C1-C6)烷基和(C1-C6)烷基羰基; R10和R11独立地选自H和(C1-C6)烷基; R12选自H,(C1-C6)烯基和(C2-C6)炔基; 4.X,Y和Z独立地选自H,卤素,氰基,硫代氰基,异硫氰基和(C 1 -C 4)烷基磺酰氧基,条件是X,Y和Z都不都是H;和4。 b)农学上可接受的媒介物,其中该组合物主要不含式(I)的化合物,其中R 1在立体化学上长于R 2。进一步描述了其制备方法,控制植物病原性真菌的方法以及产生其相应异构体(R)和(S)的外消旋混合物的方法。

著录项

  • 公开/公告号AR007419A1

    专利类型

  • 公开/公告日1999-10-27

    原文格式PDF

  • 申请/专利权人 ROHM AND HAAS COMPANY;

    申请/专利号AR1997P102680

  • 发明设计人

    申请日1997-06-18

  • 分类号A01N43/40;A01N37/18;A01N37/20;A01N37/34;C07C233/66;C07C233/76;C07C235/44;C07C255/57;C07C261;C07C309/64;C07C331/12;C07C331/20;C07D213/82;

  • 国家 AR

  • 入库时间 2022-08-22 02:28:24

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