首页> 外国专利> Pirimidilmetil sulfonamide Compounds, a process for their preparation, compositions, Methods of treatment which the agricultural uses of fungi, Pest Control and Protection of Seeds and Seeds that are used to understand.

Pirimidilmetil sulfonamide Compounds, a process for their preparation, compositions, Methods of treatment which the agricultural uses of fungi, Pest Control and Protection of Seeds and Seeds that are used to understand.

机译:Pirimidilmetil磺酰胺化合物,其制备方法,组合物,真菌在农业上的使用,病虫害的控制和种子的保护以及种子的理解。

摘要

Pirimidilmetil sulfonamide compounds and their n-oxides and agriculturally acceptable salts, their food and their salts Also acceptable Agricultural compositions comprising at least one of these compounds as the active ingredient, and also their use for controlling harmful fungi. Also, a method for Control of Arthropod pests.Claim 1: pirimidilmetil sulfonamide compounds of formula wherein are: (1) where n is Zero, One, two or three; r1 is c1-4 alkyl, halogen, haloalquilo c1-4 alkoxy, c1-4, haloalcoxi c1-4 alkyl, C1 - 4 - Uncle, haloalquil C1 - 4 - Uncle, c1-4 alkyl - sulfinilo, haloalquil c1-4 Sul Finilo, c1-4 alkyl Sulfonyl -, haloalquil c1-4 alkyl sulfonyl amino -,, C1 - 4 - aminoDi (c1-4 alkyl) amino, c1-4 alkoxy c1-4 alkyl, haloalcoxi c1-4 alkyl alquenilo C1 - C2 - 4, 4, 4 alquinilo C2 - C3 - 8 alkyl, cycloalkyl or C1 - C3 - C4 - cicioalquilo 8; and / or R1 is United to a radical a carbon Atom adjacent to a nitrogen atom of the pyrimidine Ring can form along co The n Atom and a carbon atom of aromatic nitrogen heterocycle FUSED Five membered.It may contain one, two or three nitrogen Atoms as Ring members; or Radicals R1 that are attached to two adjacent carbon Atoms of the pyrimidine Ring May form along with the carbon Atoms of a benzene Ring FUSED, FUSED or partial saturated carbociclo Unsaturated easily 5, 6 or 7 members or a FUSED heterocycle of 5, 6 or 7 members contains One,Two or three heteroatoms selected from the group consisting of 2 nitrogen ATOMS, one Oxygen Atom and a Sulfur Atom as Ring members, being possible to take one or two FUSED Ring radical selected from the group consisting of halogen, c1-4 alkyl, halometilo C1-4 alkoxy, or halometoxi; R2 is Hydrogen, c1-4 alkyl, haloalquilo c1-4 alkoxy, c1-4, haloalcoxi c1-4,C1-4 alkyl amino -, di (c1-4 alkyl) amino, c1-4 alkoxy c1-4 alkyl, haloalcoxi c1-4 alkyl alquenilo C1 - C2 - 4, 4, 4 alquinilo haloalquenilo C2, C2 - C3 - 8 4, cycloalkyl alkyl, cycloalkyl C1 - C3 - 4 - 8 where the rest or benzyl, phenyl or benzyl substituted is not 1, 2, 3, 4 or 5 replacement Either selected from the group consisting of Ciano, c1-4 alkyl, halogen, haloalquilo c1-4,C1-4 alkoxy, haloalcoxi c1-4 (c1-4 alkoxy carbonyl) and di (c1-4 alkyl aminocarbonilo phenylene); it is, heteroarendiu00edlo of 5 or 6 members, where the heteroarendiu00edlo contains One, two, three or four hetero Atoms selected from the group consisting of 1, 2, 3 or 4 Atoms Nitrogen, 1 atom of Oxygen Igeno and one Sulfur Atom, as members of the ring, where heteroarendiu00edlo phenylene and, for its part,They are not replaced or 1, 2, 3 or 4 substituents ra, each selected from the group consisting of Ciano, c1-4 alkyl, halogen, haloalquilo c1-4 alkoxy, c1-4, haloalcoxi C1 - C2 - 4, alquenilo haloalquenilo C2 - 4, 4, 4 haloalquinilo alquinilo C2, C2 - 4 (c1-4 alkoxy alkyl carbonyl (C1) and di - 4) aminocarbonilo, or is alcandiu00edlo haloalcandiu00edlo C1 C1 - 8 - 8 - 8 haloalquendiu00edlo alquendiu00edlo C2, C1 - 8Alquindiu00edlo haloalquindiu00edlo C2 or C2 - 8 - 8, where the last six Radicals mentioned above are not replaced or carry One, two or three substituents RAA, each selected from the group consisting of Ciano, c1-4 alkoxy, haloalcoxi (c1-4 alkoxy, c1-4 alkyl carbonyl (C1) and di - 4) aminocarbonilo; R3 is Hydrogen, c1-4 alkoxy, haloalcoxi c1-4 alkyl, C1 - 4 - Uncle, Uncle haloalquil c1-4 alkyl, C1 - 4 - aminoDi (c1-4 alkyl (alkyl) amino carbonyl (c1-4), c1-4 alkoxy) iminometilo, acrilou00edlo (vinilcarbonilo cycloalkyl) alkyl C1 - C3 - 4 - 8 - 8 cicloalquenilo or cycloalkyl C3, C5 - 8, Benzyl, phenyl, phenoxy, phenylthio, a heteroaryl radical 5 or 6 members, where the Ring heteroaryl has 1, 2, 3 or 4 Hetero Atoms selected from the group consisting of 1, 2, 3 or 4 nitrogen Atoms.1 1 atom of oxygen and sulfur Atom, as members of the ring, making it possible for the ring and the Ring heteroaryl phenyl, Benzyl, phenylthio substituted phenoxy and not be or be replaced with one, two or three substituents RB, each selected from the group consisting of cyano, Nitro, Mino, c1-4 alkyl, halogen, haloalquilo c1-4 alkoxy, c1-4, haloalcoxi c1-4 (c1-4 alkoxy carbonyl)Di (c1-4 alkyl) aminocarbonilo c1-4 alkyl, tio, c1-4 alkyl - and sulfinilo c1-4 alkyl sulfonyl radical heteroariloxi -; or a 5 or 6 members or a radical heteroariltio 5 or 6 members, where the Ring heteroaryl radical in the last two mentioned has 1, 2 3 or 4 heteroatoms selected And the group consisting of 1, 2, 3 or 4 nitrogen Atoms.1 Oxygen Atom and a Sulfur Atom, as members of the ring, The Ring remains possible for heteroaromu00e1tico Carry One, two or three substituents RB; or when it is heteroarendiu00edlo phenylene or 5 or 6 members, together with an ra R3 radical radical can form along with the Atoms of CA Rbono to which is attached to a benzene Ring FUSEDWhere the FUSED benzene Ring may not be changed or can take 1, 2 or 3 substituents selected independently between themselves, the group is Halogen, Nitro, cyano, c1-4 alkyl, haloalquilo c1-4 alkoxy, c1-4, haloalcoxi (c1-4 alkoxy, c1-4) di (alkyl carbonyl and C1 Aminocarbonilo - 4), or when it is heteroarendiu00edlo phenylene or 5 or 6 members.The R3 radical can also be alquenilo c1-4 alkyl, or alquinilo C2 C2 - 4 - 4 and the n-oxides and agriculturally acceptable salts, the salts acceptable Veterinary compounds of the formula (1).Claim 13: a process for preparing compounds of formula pirimidilmetil sulfonamide (1) According to claim 1, characterized in that it comprises reacting a compound of formula (2) aminometilpirimidina in which n, R1 and R2 are as defined in the re Ivindicaciu00f3n 1In basic conditions with a sulfonic acid derivative of the formula (3) in which a and R3 are as defined in claim 1 and L is Hydroxy or Halogen.
机译:吡虫腈甲磺酰胺化合物及其正氧化物和农业上可接受的盐,其食物及其盐也可接受的农业组合物,其包含这些化合物中的至少一种作为活性成分,以及它们在防治有害真菌中的用途。另外,一种节肢动物害虫的防治方法。权利要求1:下式的吡虫腈甲磺酰胺化合物,其中:(1)其中n为零,一,二或三; r1是c1-4烷基,卤素,卤代alquilo c1-4烷氧基,c1-4,卤代alcoxi c1-4烷基,C1-4-叔叔,卤代烷C1-4-叔叔,c1-4烷基-亚砜基,卤代c1-4 Finilo,c1-4烷基磺酰基-,卤代c1-4烷基磺酰基氨基-,C1-4-氨基二(c1-4烷基)氨基,c1-4烷氧基c1-4烷基,卤代醇c1-4烷基烷基C1-C2 -4、4、4、4、4、4、8、8、8-8个烷基,环烷基或C1-C3-C4的西喹啉基8;和/或R1与一个基团相连,一个嘧啶环的氮原子可以沿着co形成一个碳原子。n原子与芳族氮杂环的碳原子FUSED五元原子,它可以包含一个,两个或三个氮原子原子作为环成员;与嘧啶环的两个相邻碳原子连接的基团R1或基团R1可能与苯环的FUSED,FUSED或部分饱和carbociclo的碳原子容易地形成不饱和的5、6或7成员或FUSED杂环5、6或7个成员包含一个,两个或三个选自2个氮原子,一个氧原子和一个硫原子的杂原子作为环成员,可以带有一个或两个选自卤素,c 1-的FUSED环自由基4烷基,卤代C1-4烷氧基或卤代毒素; R 2是氢,C 1-4烷基,卤代alquilo c1-4烷氧基,c 1-4,卤代烷氧基c 1-4,C 1-4烷基氨基,二(c 1-4烷基)氨基,c 1-4烷氧基,c 1-4烷基,卤代烷氧基C 1-4烷基Alquenilo C1-C2-4、4、4 Alquinilo卤代Alquenilonilo C2,C2-C3-8、4,环烷基烷基,环烷基C1-C3-4-8,其中其余或未被苄基,苯基或苄基取代的1, 2、3、4或5个取代基选自Ciano,c1-4烷基,卤素,卤代alquilo c1-4,C1-4烷氧基,卤代醇c1-4(c1-4烷氧基羰基)和二(c1- 4-烷基氨基羰基亚苯基);它是5个或6个成员的杂原子,其中杂原子包含一个,两个,三个或四个杂原子,该杂原子选自1、2、3或4个原子氮,1个氧原子和1个氧原子。硫原子,作为环的成员,其中杂芳烃基和亚芳基未被取代或具有1、2、3或4个取代基ra,每个取代基选自Ciano,c1-4烷基,卤素,卤代alquilo c1-4烷氧基,c1-4,卤代alcoxi C1-4-4,alquenilo卤代alquenilo C2-4、4、4、4卤代喹啉alquinilo C2,C2-4(c1-4烷氧基烷基羰基(C1)和di-4)氨基碳基或alcandi u00edlo haloalcandi u00edlo C1 C1-8-8-8 haloalquendi u00edlo alquendi u00edlo C2,C1-8 Alquindi u00edlo haloalquindi u00edlo C2或C2-8-8,其中上述最后六个自由基不是取代或带有一个,两个或三个取代基RAA,每个取代基选自Ciano,c1-4烷氧基,卤代醇(c1-4烷氧基,c1-4烷基bonyl(C1)and di-4)aminocarbonilo; R 3是氢,c 1-4烷氧基,卤代醇c 1-4烷基,C 1-4-叔叔,卤代叔叔c 1-4烷基,C 1-4-氨基Di(c 1-4烷基(烷基)氨基羰基(c 1-4),c 1 -4烷氧基)亚氨基metilo,a啶基(vinilcarbonilo环烷基)烷基C1-C3-4-8-8环氯萘基或环烷基C3,C5-8,苄基,苯基,苯氧基,苯硫基,杂芳基5或6个成员,其中环杂芳基具有1、2、3或4个杂原子,这些杂原子选自1、2、3或4个氮原子。11个氧原子和硫原子作为环的成员,这使得该环和环杂芳基苯基,苄基,苯硫基取代的苯氧基并且不被或取代为一个,两个或三个取代基RB,每个取代基选自氰基,硝基,美浓,c1-4烷基,卤素,卤代alquilolo c1-4烷氧基,c1-4,卤代烷氧基c1-4(c1-4烷氧基羰基)二(c1-4烷基)氨基羰基c1-4烷基,tio,c1-4烷基-和亚磺酰基c1-4烷基磺酰基杂芳基-;或5或6个成员或5或6个基团的杂芳基,其中最后两个提到的环杂芳基基团具有1、2、3或4个杂原子,并且该基团包括1、2、3或4个氮原子。氧原子和硫原子作为环的成员,对于杂芳香族来说,该环仍然可能带有一个,两个或三个取代基RB;或者是杂芳基或五或六员亚芳基时,连同与苯环FUSED相连的CA Rbono原子一起可以形成ra R3自由基,其中FUSED苯环可能不会改变或可以彼此独立选择的1个,2个或3个取代基,该基团是卤素,硝基,氰基,c1-4烷基,卤代alquilo c1-4烷氧基,c1-4,卤代烷氧基(c1-4烷氧基,c1-4)二(烷基羰基和C1氨基羰基-4),或者是杂芳基或杂芳基亚苯基或5或6 R 3基团也可以是alquenilo c1-4烷基或alquinilo C2 C2-4-4以及正氧化物和农业上可接受的盐,这些盐是式(1)的兽用化合物。权利要求13:制备方法2.根据权利要求1的方法,其特征在于,所述方法包括使式(2)的氨基甲吡pi啶胺化合物(其中n,R 1和R 2如上定义)在碱性条件下与磺酸反应。其中a和R3如权利要求1所定义且L为羟基或卤素的式(3)的酸衍生物。

著录项

  • 公开/公告号AR063903A1

    专利类型

  • 公开/公告日2009-02-25

    原文格式PDF

  • 申请/专利权人 BASF AKTIENGESELLSCHAFT;

    申请/专利号AR2007P105191

  • 发明设计人

    申请日2007-11-22

  • 分类号C07D239/26;C07D401/12;C07D403/12;C07D405/12;C07D409/12;

  • 国家 AR

  • 入库时间 2022-08-21 19:28:44

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号