SOLID FORMS OF AN AZOCYCLIC AMIDE
    41.
    发明申请
    SOLID FORMS OF AN AZOCYCLIC AMIDE 有权
    AZOCYCLIC酰胺的固体形式

    公开(公告)号:US20120034315A1

    公开(公告)日:2012-02-09

    申请号:US13265138

    申请日:2010-04-19

    摘要: Disclosed are solid forms of 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone (Compound 1). Methods for the preparation of solid forms of Compound 1 and for the conversion of one solid form of Compound 1 into another are disclosed.Disclosed are fungicidal compositions comprising a fungicidally effective amount of a solid form of Compound 1 and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid carriers. Compositions comprising a mixture of a solid form of Compound 1 and at least one other fungicide or insecticide are also disclosed.Also disclosed are methods for controlling plant diseases caused by fungal plant pathogens comprising applying to a plant or portion thereof, or to a plant seed, a fungicidally effective amount of a solid form of Compound 1.

    摘要翻译: 公开了1- [4- [4- [5-(2,6-二氟苯基)-4,5-二氢-3-异恶唑基] -2-噻唑基] -1-哌啶基] -2- [5- (三氟甲基)-1H-吡唑-1-基]乙酮(化合物1)。 公开了制备化合物1的固体形式和将一种固体形式的化合物1转化成另一种的方法。 公开了包含杀真菌有效量的固体形式的化合物1和至少一种选自表面活性剂,固体稀释剂和液体载体的另外的组分的杀真菌组合物。 还公开了包含固体形式的化合物1和至少一种其它杀真菌剂或杀虫剂的混合物的组合物。 还公开了用于控制由真菌植物病原体引起的植物疾病的方法,包括向植物或其部分或植物种子施用杀真菌有效量的化合物1的固体形式。

    Process for Making 3-Substituted 2-Amino-5-Halobenzamides
    42.
    发明申请
    Process for Making 3-Substituted 2-Amino-5-Halobenzamides 有权
    3-取代的2-氨基-5-卤代苯甲酰胺的制备方法

    公开(公告)号:US20090306372A1

    公开(公告)日:2009-12-10

    申请号:US12373651

    申请日:2007-06-27

    摘要: Disclosed is a method for preparing a compound of Formula 1 by contacting compound of Formula 2 with R1—NH2 in the presence of a carboxylic acid and a method for preparing a compound of Formula 2 by contacting a compound of Formula 4 with phosphorus tribromide. wherein R1 is H, C1-C4 alkyl, cyclopropyl, cyclopropylmethyl or methylcyclopropyl; R2 is CH3 or Cl; R3 is C1-C6 alkyl or C3-C6 alkenyl, each optionally substituted with up to 3 halogen and up to 1 phenyl; and X is Cl or Br. Also disclosed is a method for preparing a compound of Formula 5 wherein R4, R5, R6 and Z are as defined in the disclosure, using a compound of Formula 1 that is characterized by preparing the compound of Formula 1 by the method above.

    摘要翻译: 公开了通过在羧酸存在下使式2的化合物与R 1 -NH 2接触来制备式1化合物的方法和通过使式4的化合物与三溴化磷接触来制备式2的化合物的方法。 其中R1是H,C1-C4烷基,环丙基,环丙基甲基或甲基环丙基; R2是CH3或Cl; R 3是C 1 -C 6烷基或C 3 -C 6烯基,各自任选被至多3个卤素和至多1个苯基取代; X为Cl或Br。 还公开了制备式5化合物的方法,其中R 4,R 5,R 6和Z如本公开所定义,使用式1化合物,其特征在于通过上述方法制备式1化合物。

    Process for the manufacture of 2,3-dichloropyridine
    44.
    发明申请
    Process for the manufacture of 2,3-dichloropyridine 审中-公开
    2,3-二氯吡啶的制备方法

    公开(公告)号:US20070161797A1

    公开(公告)日:2007-07-12

    申请号:US10583635

    申请日:2005-01-21

    申请人: Rafael Shapiro

    发明人: Rafael Shapiro

    IPC分类号: C07D213/61

    摘要: A method for preparing 2,3-dichloropyridine is disclosed in which 3-amino-2-chloropyridine is contacted with an alkali metal nitrite in the presence of aqueous hydrochloric acid to form a diazonium salt; and the diazonium salt is subsequently decomposed in the presence of copper catalyst wherein at least about 50% of the copper is the copper(II) oxidation state.

    摘要翻译: 公开了一种制备2,3-二氯吡啶的方法,其中3-氨基-2-氯吡啶与碱金属亚硝酸盐在盐酸水溶液的存在下接触以形成重氮盐; 随后在铜催化剂存在下分解重氮盐,其中至少约50%的铜是铜(II)氧化态。