摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-(2-{4-[3-(benzyloxy)phenylthio]-2-chlorophenyl}ethyl)-2-methylmalonic acid diethyl ester | 676481-40-6

中文名称
——
中文别名
——
英文名称
2-(2-{4-[3-(benzyloxy)phenylthio]-2-chlorophenyl}ethyl)-2-methylmalonic acid diethyl ester
英文别名
ethyl 4-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-ethoxycarbonyl-2-methylbutyrate;Diethyl 2-[2-[2-chloro-4-(3-phenylmethoxyphenyl)sulfanylphenyl]ethyl]-2-methylpropanedioate
2-(2-{4-[3-(benzyloxy)phenylthio]-2-chlorophenyl}ethyl)-2-methylmalonic acid diethyl ester化学式
CAS
676481-40-6
化学式
C29H31ClO5S
mdl
——
分子量
527.081
InChiKey
HVBVCBLAOBKTMX-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:
    633.4±55.0 °C(Predicted)
  • 密度:
    1.24±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.7
  • 重原子数:
    36
  • 可旋转键数:
    14
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    87.1
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    3-[3-(苄氧基)苯基硫代]-6-乙烯基-1-氯苯甲基丙二酸二乙酯caesium carbonate 作用下, 以 二甲基亚砜 为溶剂, 反应 0.5h, 以96%的产率得到2-(2-{4-[3-(benzyloxy)phenylthio]-2-chlorophenyl}ethyl)-2-methylmalonic acid diethyl ester
    参考文献:
    名称:
    An efficient total synthesis of a sphingosine-1-phosphate receptor agonist KRP-203
    摘要:
    An efficient total synthesis of the S1P(1) agonist, KRP-203, is described. The key step involves the conjugate addition of diethyl acetamidomalonate to a styrene compound to give the core structure of KRP-203. Multigram quantities of the targeted KRP-203, sufficient for several biological studies, were obtained in six steps with an overall yield of 58%. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.01.086
点击查看最新优质反应信息

文献信息

  • Amino alcohol derivative, addition salt thereof, and immunosuppressant
    申请人:Kohno Yasushi
    公开号:US20060135622A1
    公开(公告)日:2006-06-22
    An amino alcohol derivative represented by the following general formula (1) (for example, (±)-2-amino-5-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-methylpentane-1-ol) exhibits strong immunosuppressive effect while causing less side effects:
    下列通式(1)所代表的氨基醇衍生物(例如,(±)-2-氨基-5-[4-(3-苄氧基苯基硫基)-2-氯苯基]-2-甲基戊醇)表现出强烈的免疫抑制作用,同时引起较少的副作用。
  • Aminophosphonic acid derivatives, addition salts thereof and sip receptor modulators
    申请人:Kohno Yasushi
    公开号:US20060160771A1
    公开(公告)日:2006-07-20
    Aminophosphonic acid derivatives (e.g., 2-amino-5-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-methylpentylphosphonate monoester) are represented by the following general formula (1): and act as effective S1P receptor modulators while posing less side effects.
    氨基膦酸衍生物(例如,2-氨基-5-[4-(3-苄氧基苯基硫)-2-氯苯基]-2-甲基戊基膦酸单酯)由以下通式(1)表示,并作为有效的S1P受体调节剂,同时产生较少的副作用。
  • Aminophosphonic acid derivative, salt thereof, and modulator of sip receptor
    申请人:Kohno Yasushi
    公开号:US20080275008A1
    公开(公告)日:2008-11-06
    Aminophosphonic acid derivatives (e.g., 2-amino-5-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-methylpentylphosphonate monoester) are represented by the following general formula (1): and act as effective S1P receptor modulators while posing less side effects.
    氨基膦酸衍生物(例如,2-氨基-5-[4-(3-苄氧基苯基硫基)-2-氯苯基]-2-甲基戊基膦酸单酯)由以下一般式(1)表示,并作为有效的S1P受体调节剂,同时产生较少的副作用。
  • Amino alcohol derivatives, salts thereof and immunosuppresive agents
    申请人:Kohno Yasushi
    公开号:US20090156653A1
    公开(公告)日:2009-06-18
    An amino alcohol derivative represented by the following general formula (1) (for example, (±)-2-amino-5-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-methylpentane- 1 -ol) exhibits strong immunosuppressive effect while causing less side effects:
    以下是一种氨基醇衍生物的通用式(1)(例如,(±)-2-氨基-5-[4-(3-苄氧基苯基硫基)-2-氯苯基]-2-甲基戊烷-1-醇),它表现出强烈的免疫抑制作用,同时引起较少的副作用:
  • AMINO ALCOHOL DERIVATIVE, ADDITION SALT THEREOF, AND IMMUNOSUPPRESSANT
    申请人:Kyorin Pharmaceutical Co., Ltd.
    公开号:EP1548003A1
    公开(公告)日:2005-06-29
    An amino alcohol derivative represented by the following general formula (1) (for example, (±)-2-amino-5-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-methylpentane-1-ol) exhibits strong immunosuppressive effect while causing less side effects:
    由以下通式(1)代表的氨基醇衍生物(例如,(±)-2-氨基-5-[4-(3-苄氧基苯硫基)-2-氯苯基]-2-甲基戊-1-醇)具有很强的免疫抑制作用,同时副作用较小:
查看更多