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2,5-dichloro-4-isopropoxypyrimidine | 1351762-13-4

中文名称
——
中文别名
——
英文名称
2,5-dichloro-4-isopropoxypyrimidine
英文别名
2,5-dichloro-4-propan-2-yloxypyrimidine
2,5-dichloro-4-isopropoxypyrimidine化学式
CAS
1351762-13-4
化学式
C7H8Cl2N2O
mdl
——
分子量
207.059
InChiKey
ZQFKLIHXNBEAHA-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:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    35
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    异丙醇2,4,5-三氯嘧啶 在 sodium hydride 作用下, 以 四氢呋喃 、 mineral oil 为溶剂, 以84.2 %的产率得到2,5-dichloro-4-isopropoxypyrimidine
    参考文献:
    名称:
    [EN] INHIBITORS OF CYCLIN-DEPENDENT KINASE (CDK) 12 AND/OR CDK13 AND USES THEREOF
    [FR] INHIBITEURS DE KINASE 12 DÉPENDANTE DE LA CYCLINE (CDK) ET/OU CDK13 ET LEURS UTILISATIONS
    摘要:
    Described herein are inhibitors of cyclin-dependent kinase (CDK) 12 and/or CDK13 (and pharmaceutical compositions comprising the inhibitors. The subject compounds and compositions are useful for the treatment of a disease or disorder associated with overexpression of CDK 12 and/or CDK13.
    公开号:
    WO2024032561A1
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文献信息

  • 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] 2-PHENYLAMINOPYRIMIDINE DERIVATIVES AS KINASE LRRK2 MODULATORS FOR THE TREATMENT OF PARKINSON'S DISEASE<br/>[FR] DÉRIVÉS 2-PHÉNYLAMINOPYRIMIDINES EN TANT QUE MODULATEURS DE KINASE LRRK2 POUR LE TRAITEMENT DE LA MALADIE DE PARKINSON
    申请人:HOFFMANN LA ROCHE
    公开号:WO2013079494A1
    公开(公告)日:2013-06-06
    Specific Compounds of formula (I): or pharmaceutically acceptable salts thereof, wherein m, X, R, R2, R3, R, R6 and R7 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.
    具有以下化学式(I)的特定化合物:或其药用可接受的盐,其中m、X、R、R2、R3、R、R6和R7如本文所定义。还公开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。
  • 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。
  • 2-PHENYLAMINOPYRIMIDINE DERIVATIVES AS KINASE LRRK2 MODULATORS FOR THE TREATMENT OF PARKINSON'S DISEASE
    申请人:F.Hoffmann-La Roche AG
    公开号:EP2785699A1
    公开(公告)日:2014-10-08
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