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6-[(4,5-Dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile, acetic acid salt (1:1) | 745048-53-7

中文名称
——
中文别名
——
英文名称
6-[(4,5-Dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile, acetic acid salt (1:1)
英文别名
AR-08 acetate;acetic acid;6-(4,5-dihydro-1H-imidazol-2-ylamino)-7-methyl-3H-benzimidazole-4-carbonitrile
6-[(4,5-Dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile, acetic acid salt (1:1)化学式
CAS
745048-53-7
化学式
C2H4O2*C12H12N6
mdl
——
分子量
300.32
InChiKey
PHBLJFKGZMOGFS-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):
    1.2
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    126
  • 氢给体数:
    4
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-(7-Cyano-4-methyl-1H-benzimidazol-5-yl-imino)-imidazolidine-1-carboxylic Acid Methyl Ester甲醇溶剂黄146 为溶剂, 反应 16.0h, 以71%的产率得到6-[(4,5-Dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile, acetic acid salt (1:1)
    参考文献:
    名称:
    Methods of making 6-[(4,5-Dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile and its preferred salt form
    摘要:
    6-[(4,5-二氢-1H-咪唑-2-基)氨基]-7-甲基-1H-苯并咪唑-4-羧腈在2,3,7-三氨基-4,6-二甲基-1,9-苝二羧腈和其无水单乙酸盐的情况下,可用于治疗α-2介导的疾病,如眼压高。
    公开号:
    US20040167194A1
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文献信息

  • Methods and Compositions for Treating ADHD
    申请人:Adams Brian K.
    公开号:US20150133516A1
    公开(公告)日:2015-05-14
    The present invention provides compositions and methods of using α2 adrenergic receptor agonists as treatments for ADHD. The α2 adrenergic receptor agonist for use with these methods is a benzimidazole derivative, and may be specifically N-(4,5-Dihydro-1H-imidazol-2-yl)-7-cyano-4-methyl-1H-benzimidazol-5-amine acetate. Formulations and routes of administration are also described.
    本发明提供了将α2肾上腺素受体激动剂用作治疗ADHD的组合物和方法。用于这些方法的α2肾上腺素受体激动剂是苯并咪唑衍生物,可能特别是N-(4,5-二氢-1H-咪唑-2-基)-7-氰基-4-甲基-1H-苯并咪唑-5-胺醋酸盐。还描述了配方和给药途径。
  • [EN] METHODS OF MAKING 6-[(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)AMINO-]-7-METHYL-1H-BENZIMIDAZOLE-4-CARBONITRILE AND ITS PREFERRED SALT FORM<br/>[FR] PROCEDES DE FABRICATION DE 6-[(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)AMINO-]-7-METHYL-1H-BENZIMIDAZOLE-4-CARBONITRILE ET FORME PREFEREE D'UN SEL DE CELUI-CI
    申请人:PROCTER & GAMBLE
    公开号:WO2004074279A1
    公开(公告)日:2004-09-02
    6-[(4,5-Dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile substantially free of 2,3,7-triamino-4,6-dimethyl-1,9-phenazinedicarbonitrile, and the anhydrous monoacetate salt thereof, are useful in the treatment of alpha-2 mediated disorders such as ocular hypertension.
    6-[(4,5-二氢-1H-咪唑-2-基)氨基]-7-甲基-1H-苯并咪唑-4-羧腈,基本上不含2,3,7-三氨基-4,6-二甲基-1,9-菲嗪二羧腈,以及其无水单乙酸盐,在治疗α-2介导的疾病,如眼压增高方面具有用处。
  • Methods of making 6-[(4,5-dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile and its preferred salt form
    申请人:Randall Lynn Jared
    公开号:US20060122248A1
    公开(公告)日:2006-06-08
    6-[(4,5-Dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile substantially free of 2,3,7-triamino-4,6-dimethyl-1,9-phenazinedicarbonitrile, and the anhydrous monoacetate salt thereof, are useful in the treatment of alpha-2 mediated disorders such as ocular hypertension.
    6-[(4,5-二氢-1H-咪唑-2-基)氨基]-7-甲基-1H-苯并咪唑-4-羧腈,基本上不含2,3,7-三氨基-4,6-二甲基-1,9-苯并二氰基的盐酸单乙酰化物,可用于治疗α-2介导的疾病,如眼压增高。
  • Methods of making 6-[(4,5-Dihydro-1H-imidazol-2-yl) amino-]-7-methyl-1H-benzimidazole-4-carbonitrile and its preferred salt form
    申请人:The Board of Regents of the University of Nebraska
    公开号:EP1953146A1
    公开(公告)日:2008-08-06
    A method of making a compound of formula (II): comprising: a) providing a compound of formula (I): b) cyclizing the formula (I) compound in a single pot by using a non ferrous metal hydrogenation catalyst, in the presence of hydrogen or a hydrogen donor, and optionally a cyclization agent, yielding the compound of formula (II).
    一种制造式(II)化合物的方法: 包括 a) 提供式(I)化合物: b) 在氢或氢供体以及可选的环化剂存在下,使用非铁金属氢化催化剂,在一锅中环化式(I)化合物,得到式(II)化合物。
  • EP1594862B1
    申请人:——
    公开号:EP1594862B1
    公开(公告)日:2008-11-19
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