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methyl 3-amino-3-(3-pyridyl)-2-propenoate | 93036-67-0

中文名称
——
中文别名
——
英文名称
methyl 3-amino-3-(3-pyridyl)-2-propenoate
英文别名
Methyl 3-amino-3-(pyridin-3-YL)prop-2-enoate;methyl 3-amino-3-pyridin-3-ylprop-2-enoate
methyl 3-amino-3-(3-pyridyl)-2-propenoate化学式
CAS
93036-67-0
化学式
C9H10N2O2
mdl
——
分子量
178.191
InChiKey
ZKNMRQGIUVHOPC-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

物化性质

  • 沸点:
    352.2±30.0 °C(Predicted)
  • 密度:
    1.182±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    65.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    methyl 3-amino-3-(3-pyridyl)-2-propenoate 在 sodium tetrahydroborate 、 溶剂黄146盐酸 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 13.0h, 以89%的产率得到3-Amino-3-pyridin-3-yl-propionic acid methyl ester; hydrochloride
    参考文献:
    名称:
    A Practical Synthesis of the Platelet Fibrinogen Antagonist, Elarofiban
    摘要:
    Elarofiban is a novel, nonpeptide, orally active fibrinogen receptor antagonist useful for the treatment of platelet mediated thrombotic disorders (Costanzo, M. J.; Hoekstra, W. J.; Maryanoff, B. E. WO, 97/41102,1997). Herein we describe the process research that was carried out for the synthesis of elarofiban that eventually led to the development of a safe and cost-effective commercial scale process.
    DOI:
    10.1021/op034103o
  • 作为产物:
    描述:
    烟酸甲酯sodium methylatesodium acetate溶剂黄146 作用下, 以 甲醇甲苯 为溶剂, 反应 17.0h, 生成 methyl 3-amino-3-(3-pyridyl)-2-propenoate
    参考文献:
    名称:
    A Practical Synthesis of the Platelet Fibrinogen Antagonist, Elarofiban
    摘要:
    Elarofiban is a novel, nonpeptide, orally active fibrinogen receptor antagonist useful for the treatment of platelet mediated thrombotic disorders (Costanzo, M. J.; Hoekstra, W. J.; Maryanoff, B. E. WO, 97/41102,1997). Herein we describe the process research that was carried out for the synthesis of elarofiban that eventually led to the development of a safe and cost-effective commercial scale process.
    DOI:
    10.1021/op034103o
  • 作为试剂:
    描述:
    烟酰乙酸甲酯异丙醇甲酸methyl 3-amino-3-(3-pyridyl)-2-propenoate甲苯 作用下, 以 甲苯 为溶剂, 反应 2.25h, 以resulted in 77.74 g (88.8%) of methyl 3-amino-3-(3-pyridyl)-2-propenoate as colorless crystals的产率得到methyl 3-amino-3-(3-pyridyl)-2-propenoate
    参考文献:
    名称:
    Process for preparing [S- (R*, S*) ] -beta- [ [ [1- [1-oxo-3- (4-piperidinyl) propyl] -3-piperidinyl] carbonyl]amino] -3-pyridinepropanoic acid and derivatives
    摘要:
    一种制备式I1化合物的过程,其中R1和R2是独立选择自氢、低烷基和卤素的基团。
    公开号:
    US20020137937A1
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文献信息

  • Process for preparing [S-(R*,S*)]-&bgr;-[[[1-[1-oxo-3(4-piperidinyl)propyl]-3-piperidinyl]carbonyl]amino]-3-pyridinepropanoic acid and derivatives
    申请人:——
    公开号:US06515130B1
    公开(公告)日:2003-02-04
    A process for preparing a compound of formula I wherein R1 and R2 are independently selected from the group consisting of hydrogen, lower alkyl and halogen
    一种制备化合物I的方法,其中R1和R2是独立地选择自氢、低级烷基和卤素的群组。
  • A Practical Synthesis of the Platelet Fibrinogen Antagonist, Elarofiban
    作者:Judith H. Cohen、Mary Ellen Bos、Sergio Cesco-Cancian、Bruce D. Harris、John T. Hortenstine、Michael Justus、Cynthia A. Maryanoff、John Mills、Stefan Muller、Armin Roessler、Lorraine Scott、Kirk L. Sorgi、Frank J. Villani,、Robin R. H. Webster、Christian Weh
    DOI:10.1021/op034103o
    日期:2003.11.1
    Elarofiban is a novel, nonpeptide, orally active fibrinogen receptor antagonist useful for the treatment of platelet mediated thrombotic disorders (Costanzo, M. J.; Hoekstra, W. J.; Maryanoff, B. E. WO, 97/41102,1997). Herein we describe the process research that was carried out for the synthesis of elarofiban that eventually led to the development of a safe and cost-effective commercial scale process.
  • Process for preparing [S- (R*, S*) ] -beta- [ [ [1- [1-oxo-3- (4-piperidinyl) propyl] -3-piperidinyl] carbonyl]amino] -3-pyridinepropanoic acid and derivatives
    申请人:——
    公开号:US20020137937A1
    公开(公告)日:2002-09-26
    A process for preparing a compound of formula I 1 wherein R 1 and R 2 are independently selected from the group consisting of hydrogen, lower alkyl and halogen
    一种制备式I1化合物的过程,其中R1和R2是独立选择自氢、低烷基和卤素的基团。
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