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硫酸氢伊伐布雷定 | 1202000-62-1

中文名称
硫酸氢伊伐布雷定
中文别名
——
英文名称
ivabradine hydrogensulfate
英文别名
ivabradine sulfate;Ivabradine monosulfate;3-[3-[[(7S)-3,4-dimethoxy-7-bicyclo[4.2.0]octa-1,3,5-trienyl]methyl-methylamino]propyl]-7,8-dimethoxy-2,5-dihydro-1H-3-benzazepin-4-one;sulfuric acid
硫酸氢伊伐布雷定化学式
CAS
1202000-62-1
化学式
C27H36N2O5*H2O4S
mdl
——
分子量
566.673
InChiKey
BTPJWGWDKZFLCT-ZMBIFBSDSA-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):
    2.66
  • 重原子数:
    39
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    143
  • 氢给体数:
    2
  • 氢受体数:
    10

反应信息

  • 作为产物:
    描述:
    伊伐布雷定硫酸 作用下, 以 异丙醇 为溶剂, 反应 1.0h, 生成 硫酸氢伊伐布雷定
    参考文献:
    名称:
    [EN] ACID ADDITION SALTS OF IVABRADINE AND PREPARATION METHOD THEREOF
    [FR] SELS D'ADDITION D'ACIDE DE L'IVABRADINE ET LEUR PRÉPARATION
    摘要:
    公开号:
    WO2011104723A3
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文献信息

  • METHODS FOR THE PREPARATION OF IVABRADINE SULFATE AND FORM I CRYSTAL THEREOF
    申请人:Sun Piaoyang
    公开号:US20110275614A1
    公开(公告)日:2011-11-10
    Methods for the preparation of Ivabradine sulfate and form I crystal thereof. In particular, the Ivabradine sulfate and the preparation methods thereof, and the stable form I crystal of Ivabradine sulfate and the preparation methods thereof.
    制备伊伐布雷定硫酸盐及其I型晶体的方法。具体而言,是关于伊伐布雷定硫酸盐及其制备方法,以及伊伐布雷定硫酸盐的稳定I型晶体及其制备方法的。
  • Process for the preparation of functionalised benzocyclobutenes, and application in the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid
    申请人:Peglion Jean-Louis
    公开号:US20100016580A1
    公开(公告)日:2010-01-21
    Process for the preparation of compounds of formula (IV): wherein R 1 , R 2 , R 3 and R 4 , which may be identical or different, each represent a hydrogen atom, a linear or branched (C 1 -C 6 )alkyl group, a linear or branched (C 1 -C 6 )alkoxy group, a fluorine atom, a chlorine atom, a protected amine group, a protected hydroxyl group, an alkoxycarbonyl group in which the alkoxy group is linear or branched (C 1 -C 6 ), or a CF 3 group, or R 1 ═R 4 ═H and R 2 and R 3 together with the carbon atoms carrying them form a 1,3-dioxolane group, R 5 represents a saturated or unsaturated, linear or branched (C 1 -C 6 )alkyl group, a linear or branched (C 1 -C 6 )hydroxyalkyl group in which the hydroxyl function is protected, or a CO 2 R 7 group in which R 7 is a linear or branched (C 1 -C 6 )alkyl group, R 6 represents a cyano group or a CO 2 R 8 group in which R 8 is a linear or branched (C 1 -C 6 )-alkyl group. Application in the synthesis of ivabradine, addition salts thereof with a pharmaceutically acceptable acid and hydrates thereof.
    制备式(IV)化合物的过程: 其中R1,R2,R3和R4可以相同也可以不同,分别表示氢原子,线性或支链(C1-C6)烷基,线性或支链(C1-C6)烷氧基,原子,原子,保护胺基,保护羟基,其中烷氧基是线性或支链的(C1-C6)烷氧基,或CF3基团,或R1═R4═H,而R2和R3与携带它们的碳原子形成1,3-二氧杂环烷基; R5表示饱和或不饱和的线性或支链(C1-C6)烷基,线性或支链(C1-C6)羟基烷基,其中羟基功能被保护,或CO2R7基团,其中R7是线性或支链(C1-C6)烷基, R6表示基或CO2R8基团,其中R8是线性或支链(C1-C6)烷基。 应用于伊伐布雷定的合成,以及其与药用酸的加合物和合物的制备。
  • PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID
    申请人:PEGLION Jean-Louis
    公开号:US20120208996A1
    公开(公告)日:2012-08-16
    Process for the synthesis of ivabradine of formula (I): and addition salts thereof with a pharmaceutically acceptable acid.
    公式(I)的伊伐布地那合成过程以及其与药用可接受酸的加成盐。
  • Process for the synthesis of 3,4-dimethoxybicyclo[4.2.0]OCTA-1,3,5-triene-7-carbonitrile, and application in the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid
    申请人:Les Laboratoires Servier
    公开号:US08859763B1
    公开(公告)日:2014-10-14
    Process for the synthesis of the compound of formula (I): Application in the synthesis of ivabradine, addition salts thereof with a pharmaceutically acceptable acid and hydrates thereof.
    合成式(I)化合物的过程:用于伊伐布雷定的合成,其与药学上可接受的酸的加成盐及其合物。
  • Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid
    申请人:Peglion Jean-Louis
    公开号:US20100249398A1
    公开(公告)日:2010-09-30
    Process for the synthesis of ivabradine of formula (I): and addition salts thereof with a pharmaceutically acceptable acid.
    公式(I)的伊伐布地那的合成过程,以及与药用可接受酸的加成盐。
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