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2,3-Didehydrotyrosine, (Z)- | 1189182-30-6

中文名称
——
中文别名
——
英文名称
2,3-Didehydrotyrosine, (Z)-
英文别名
(Z)-2-amino-3-(4-hydroxyphenyl)prop-2-enoic acid
2,3-Didehydrotyrosine, (Z)-化学式
CAS
1189182-30-6
化学式
C9H9NO3
mdl
——
分子量
179.17
InChiKey
VWVGLOXKDVGAFA-YVMONPNESA-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
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    83.6
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • [EN] PROCESS FOR PRODUCING OPTICALLY ACTIVE 3-(4-HYDROXYPHENYL)PROPIONIC ACIDS<br/>[FR] PROCEDE DE PRODUCTION D'ACIDES 3-(4-HYDROXYPHENYL)PROPIONIQUES OPTIQUEMENT ACTIFS
    申请人:TAKASAGO PERFUMERY CO LTD
    公开号:WO2005051882A1
    公开(公告)日:2005-06-09
    The present invention relates to a process for producing an optically active 3-(4-hydroxyphenyl)propionic acid useful as intermediates for medicines, through short steps in good yield and with high optical purity. More specifically, the present invention relates to a process for producing an optically active 3-(4-hydroxyphenyl)propionic acid of the formula (6): wherein R2 is an alkyl group; R5 to R8 are each independently a hydrogen atom or a substituent; and the symbol * is an chiral carbon atom, or a salt thereof, which comprises reacting a benzaldehyde of the formula (1): wherein R1 is a protective group; and R5 to R8 are each the same as defined above, with a glycolic acid derivative of the formula (2): wherein R3 is a hydrocarbon group; and R2 is the same as defined above, hydrolyzing the resulting product to give a cinnamic acid of the formula (4): wherein R1, R2 and R5 to R8 are each the same as defined above, or a salt thereof, and subjecting the resulting cinnamic acid (4) or a salt thereof to asymmetric hydrogenation to give an optically active phenylpropionic acid of the formula (5): wherein all the symbols are each the same as defined above, or a salt thereof, followed by deprotection.
    本发明涉及一种生产光学活性3-(4-羟基苯基)丙酸的工艺,作为药物中间体,通过简短的步骤、高产率和高光学纯度。更具体地,本发明涉及一种生产光学活性3-(4-羟基苯基)丙酸的工艺,其化学结构如下(6):其中R2是烷基;R5至R8分别独立地是氢原子或取代基;符号*是一个手性碳原子,或其盐,包括将化学结构如下(1)的苯甲醛:其中R1是保护基;R5至R8分别与上述定义相同,与化学结构如下(2)的甘醇酸衍生物反应:其中R3是烃基;R2与上述定义相同,水解得到肉桂酸的产物:其中R1、R2和R5至R8分别与上述定义相同,或其盐,并将得到的肉桂酸(4)或其盐进行不对称氢化反应,得到光学活性苯丙酸的产物:其中所有符号均与上述定义相同,或其盐,随后进行去保护处理。
  • Process for producing optically active 3-(4-hydroxyphenyl)proprionic acids
    申请人:Yokozawa Tohru
    公开号:US20070142472A1
    公开(公告)日:2007-06-21
    The present invention relates to a process for producing an optically active 3-(4-hydroxyphenyl)propionic acid useful as intermediates for medicines, through short steps in good yield and with high optical purity. More specifically, the present invention relates to a process for producing an optically active 3-(4-hydroxyphenyl)propionic acid of the formula (6): wherein R 2 is an alkyl group; R 5 to R 8 are each independently a hydrogen atom or a substituent; and the symbol * is an chiral carbon atom, or a salt thereof, which comprises reacting a benzaldehyde of the formula (1): wherein R 1 is a protective group; and R 5 to R 8 are each the same as defined above, with a glycolic acid derivative of the formula (2): wherein R 3 is a hydrocarbon group; and R 2 is the same as defined above, hydrolyzing the resulting product to give a cinnamic acid of the formula (4): wherein R 1 , R 2 and R 5 to R 8 are each the same as defined above, or a salt thereof, and subjecting the resulting cinnamic acid (4) or a salt thereof to asymmetric hydrogenation to give an optically active phenylpropionic acid of the formula (5): wherein all the symbols are each the same as defined above, or a salt thereof, followed by deprotection.
    本发明涉及一种生产光学活性的3-(4-羟基苯基)丙酸的方法,该方法通过短步骤以良好产率和高光学纯度的方式,作为药物中间体。更具体地说,本发明涉及一种生产式(6)的光学活性3-(4-羟基苯基)丙酸的方法:其中R2是烷基;R5到R8分别独立地是氢原子或取代基;符号*是手性碳原子,或其盐,包括用式(1)的苯甲醛反应:其中R1是保护基;R5到R8分别与上述定义相同,与式(2)的乙二醇酸衍生物反应:其中R3是碳氢基团;R2与上述定义相同,水解所得产物得到式(4)的肉桂酸:其中R1、R2和R5到R8分别与上述定义相同,或其盐,并将所得的肉桂酸(4)或其盐经过不对称氢化作用得到式(5)的光学活性苯丙酸:其中所有符号均与上述定义相同,或其盐,然后去保护基。
  • BIOCOMPATIBLE POLYMERS FOR MEDIAL DEVICES
    申请人:Kohn Joachim B.
    公开号:US20120226013A1
    公开(公告)日:2012-09-06
    The present invention relates to new classes of monomeric compounds, which may be polymerized to form novel biodegradable and bioresorble polymers and copolymers. These polymers and co-polymers, while not limited thereto, may be adapted for radio-opacity and are useful for medical device applications and controlled release therapeutic formulations.
    本发明涉及新型单体化合物,可以聚合形成新颖的可生物降解和可生物吸收的聚合物和共聚物。这些聚合物和共聚物,虽然不限于此,可以适用于放射透明度,并且适用于医疗器械应用和控释治疗制剂。
  • BIOCOMPATIBLE POLYMERS FOR MEDICAL DEVICES
    申请人:Rutgers, The State University of New Jersey
    公开号:EP3461855A1
    公开(公告)日:2019-04-03
    The present invention relates to new classes of monomeric compounds, which may be polymerized to form novel biodegradable and bioresorble polymers and copolymers. These polymers and co-polymers, while not limited thereto, may be adapted for radio-opacity and are useful for medical device applications and controlled release therapeutic formulations.
    本发明涉及新型单体化合物,可通过聚合形成新型可生物降解和可生物复原的聚合物和共聚物。这些聚合物和共聚物虽然并不局限于此,但可具有放射性能力,可用于医疗器械应用和控释治疗制剂。
  • Biocompatible polymers for medical devices
    申请人:Rutgers, The State University of New Jersey
    公开号:US10202490B2
    公开(公告)日:2019-02-12
    The present invention relates to new classes of monomeric compounds, which may be polymerized to form novel biodegradable and bioresorble polymers and copolymers. These polymers and co-polymers, while not limited thereto, may be adapted for radio-opacity and are useful for medical device applications and controlled release therapeutic formulations.
    本发明涉及新型单体化合物,可通过聚合形成新型可生物降解和可生物复原的聚合物和共聚物。这些聚合物和共聚物虽然并不局限于此,但可具有放射性能力,可用于医疗器械应用和控释治疗制剂。
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