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2-chloro-5-chloro-N-isobutylpyrimidin-4-amine | 1214279-50-1

中文名称
——
中文别名
——
英文名称
2-chloro-5-chloro-N-isobutylpyrimidin-4-amine
英文别名
2,5-dichloro-N-(2-methylpropyl)pyrimidin-4-amine
2-chloro-5-chloro-N-isobutylpyrimidin-4-amine化学式
CAS
1214279-50-1
化学式
C8H11Cl2N3
mdl
——
分子量
220.101
InChiKey
ORESUEWQAHOYDT-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):
    3.4
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • 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

文献信息

  • [EN] AMINOPYRIMIDINE DERIVATIVES AS LRRK2 MODULATORS<br/>[FR] DÉRIVÉS AMINOPYRIMIDINIQUES UTILISÉS COMME MODULATEURS DE LRRK2
    申请人:HOFFMANN LA ROCHE
    公开号:WO2013079505A1
    公开(公告)日:2013-06-06
    Compounds of the formula (I): or pharmaceutically acceptable salts thereof, wherein A, X, R1, R2, R3 and R4 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)的化合物或其药用可接受的盐,其中A、X、R1、R2、R3和R4如本文所定义。还公开了制备这些化合物的方法,并将这些化合物用于治疗与LRRK2受体相关的疾病,如帕森病。
  • [EN] 2-(PHENYL OR PYRID-3-YL) AMINOPYRIMIDINE DERIVATIVES AS KINASE LRRK2 MODULATORS FOR THE TREATMENT OF PARKINSON'S DISEASE<br/>[FR] DÉRIVÉS 2-(PHÉNYL OU PYRID-3-YL)AMINOPYRIMIDINES EN TANT QUE MODULATEURS DE LA KINASE LRRK2 POUR LE TRAITEMENT DE LA MALADIE DE PARKINSON
    申请人:HOFFMANN LA ROCHE
    公开号:WO2013079495A1
    公开(公告)日:2013-06-06
    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.
    化合物的结构式(I),或其药用盐,其中m、n、X、R1、R2、R3、R4和R5的定义如本文所述。还公开了制备这些化合物的方法,并将这些化合物用于治疗与LRRK2受体相关的疾病,如帕森病。
  • 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。
  • [EN] AMINOPYRIMIDINE DERIVATIVES AS LRRK2 MODULATORS<br/>[FR] DÉRIVÉS AMINOPYRIDINES EN TANT QUE MODULATEURS DE LRRK2
    申请人:HOFFMANN LA ROCHE
    公开号:WO2013079493A1
    公开(公告)日:2013-06-06
    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.
    化合物的公式(I),或其药学上可接受的盐,其中m、n、X、R1、R2、R3、R4和R5的定义如本文所述。还公开了制备这些化合物的方法以及利用这些化合物治疗与LRRK2受体相关的疾病,例如帕森病。
  • 4-Alkyl-substituted diaminopyrimidines
    申请人:Greul Jörg Nico
    公开号:US20110230478A1
    公开(公告)日:2011-09-22
    Use of 4-alkyl-substituted diaminopyrimidines of the formula (I) as fungicide in which R 1 to R 13 and X 1 and X 2 have the meanings given in the description, and agrochemically active salts thereof, 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 diaminopyrimidines of the formulae (Ia), (Ib) and (Ic).
    使用具有以下结构的4-烷基取代二氨基嘧啶化合物(I)作为杀菌剂,其中R1至R13和X1和X2的含义如描述中所述,以及其农药活性盐,以及用于在植物内部和/或表面或植物种子内部和/或表面控制植物病原真菌的方法和组合物,用于制备这种组合物和处理种子的过程,以及它们在农业、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。此外,本发明还涉及制备具有以下结构的二氨基嘧啶化合物(Ia)、(Ib)和(Ic)的方法。
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