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2,5-dichloro-N-(cyclopropylmethyl)pyrimidine-4-amine | 1050602-59-9

中文名称
——
中文别名
——
英文名称
2,5-dichloro-N-(cyclopropylmethyl)pyrimidine-4-amine
英文别名
2,5-dichloro-N-(cyclopropylmethyl)pyrimidin-4-amine
2,5-dichloro-N-(cyclopropylmethyl)pyrimidine-4-amine化学式
CAS
1050602-59-9
化学式
C8H9Cl2N3
mdl
——
分子量
218.086
InChiKey
IOABFLAIPRWKEN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    37.8
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    盐酸2,5-dichloro-N-(cyclopropylmethyl)pyrimidine-4-amine对异丙氧基苯胺1,4-二氧六环乙腈 为溶剂, 反应 16.0h, 生成 5-chloro-N4-(cyclopropylmethyl)-N2-(4-isopropoxyphenyl)pyrimidine-2,4-diamine hydrochloride
    参考文献:
    名称:
    DIAMINOPYRIMIDINES AS FUNGICIDES
    摘要:
    使用式(I)中的二氨基嘧啶,其中R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11和X1、X2和A具有描述中所给出的含义,以及其农业化学活性盐作为杀真菌剂。式(Ia)、(Ib)、(Ic)、(Id)、(Ie)、(If)中的二氨基嘧啶,其中R8a、R8b、R8c、R8d、R8e、R8f、R3b、R3c、R3e、X1b、X1c、X1e和R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11和X1、X2和A具有描述中所给出的含义,以及其农业化学活性盐及其用于控制不良微生物。
    公开号:
    US20100081679A1
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文献信息

  • Heterocyclically Substituted Anilinopyrimides
    申请人:Greul Jörg Nico
    公开号:US20110245242A1
    公开(公告)日:2011-10-06
    Heterocyclically substituted anilinopyrimidines of the formula (I) in which R 1 to R 10 and L 1 , L 2 , E1, E2, E3, Y and Z have the meanings given in the description, and agrochemically active salts thereof, their use and also methods and compositions for controlling phytopathogenic harmful fungi in and/or on plants or in and/or on seed of plants, processes for preparing such compositions and treated seed and also their use for controlling phytopathogenic harmful fungi in agriculture, horticulture and forestry, in the protection of materials and in the domestic and hygiene field. The present invention furthermore relates to a process for preparing heterocyclically substituted anilinopyrimidinenes of the formula (I).
    公式(I)中的杂环取代苯基嘧啶,其中R1至R10和L1、L2、E1、E2、E3、Y和Z的含义如描述中所示,以及其农药活性盐,它们的用途以及用于控制植物或植物种子中和/或上的植物病原有害真菌的方法和组合物,制备这种组合物的过程以及处理后的种子以及它们在农业、园艺和林业中用于控制植物病原有害真菌,在材料保护以及家庭和卫生领域。此外,本发明还涉及制备公式(I)中的杂环取代苯基嘧啶的方法。
  • AMINOPYRIMIDINE DERIVATIVES AS LRRK2 INHIBITORS
    申请人:Baker-Glenn Charles
    公开号:US20110301141A1
    公开(公告)日:2011-12-08
    Compounds of the formula I: or pharmaceutically acceptable salts thereof, wherein m, n. X, R 1 , R 2 , R 3 , R 5 , R 6 and R 7 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with LRRK2 receptor, such as Parkinson's disease.
    化合物的公式I:或其药用盐,其中m,n,X,R1,R2,R3,R5,R6和R7的定义如本文所述。还公开了制备这些化合物的方法以及将这些化合物用于治疗与LRRK2受体相关的疾病,如帕森病。
  • Heterocyclically Substituted Anilinopyrimidines
    申请人:Wasnaire Pierre
    公开号:US20110245249A1
    公开(公告)日:2011-10-06
    Heterocyclically substituted anilinopyrimidines of the formula (I) in which R 1 to R 12 and E1, E2, E3, L 1 , Y, Z and L 2 have the meanings given in the description, and agrochemically active salts thereof, their use and also methods and compositions for controlling phytopathogenic harmful fungi in and/or on plants or in and/or on seed of plants, processes for preparing such compositions and treated seed and also their use for controlling phytopathogenic harmful fungi in agriculture, horticulture and forestry, in the protection of materials and in the domestic and hygiene field. The present invention furthermore relates to a process for preparing heterocyclically substituted anilinopyrimidinenes of the formula (I).
    公式(I)中的杂环取代苯基嘧啶,其中R1至R12和E1、E2、E3、L1、Y、Z和L2具有描述中给出的含义,以及其农用活性盐,它们的用途以及控制植物或种子中和/或植物中和/或植物种子上的植物病原真菌的方法和组合物,用于制备这种组合物的过程以及受处理的种子,以及其在农业、园艺和林业中控制植物病原真菌的用途,在材料保护以及家庭和卫生领域。本发明还涉及制备公式(I)中的杂环取代苯基嘧啶的方法。
  • AMINOPYRIMIDINE DERIVATIVES AS LRRK2 MODULATORS
    申请人:Genentech, Inc.
    公开号:US20130157999A1
    公开(公告)日:2013-06-20
    Specific Compounds of formula I: or pharmaceutically acceptable salts thereof, wherein m, X, R 1 , R 2 , R 3 , R 5 , R 6 and R 7 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with LRRK2 receptor, such as Parkinson's disease.
    公式I的特定化合物或其药学上可接受的盐,其中m,X,R1,R2,R3,R5,R6和R7的定义如本文所述。还揭示了制备这些化合物的方法,并使用这些化合物治疗与LRRK2受体相关的疾病,如帕森病。
  • 2-(PHENYL OR PYRID-3-YL) AMINOPYRIMIDINE DERIVATIVES AS KINASE LRRK2 MODULATORS FOR THE TREATMENT OF PARKINSON'S DISEASE
    申请人:F. Hoffmann-La Roche AG
    公开号:EP3121174A1
    公开(公告)日:2017-01-25
    Compounds of the formula I: or pharmaceutically acceptable salts thereof, wherein m, n. X, R1, R2, R3, R4 and R5 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with LRRK2 receptor, such as Parkinson's disease.
    式 I 的化合物: 或其药学上可接受的盐、 其中 m、n、X、R1、R2、R3、R4 和 R5 如本文所定义。还公开了制造这些化合物的方法和使用这些化合物治疗与 LRRK2 受体相关的疾病(如帕森病)的方法。
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