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t-Butyl 4-[1-(2-butynyl)-5-cyano-4-hydroxymethyl-1H-imidazol-2-yl] piperazine-1-carboxylate | 635723-38-5

中文名称
——
中文别名
——
英文名称
t-Butyl 4-[1-(2-butynyl)-5-cyano-4-hydroxymethyl-1H-imidazol-2-yl] piperazine-1-carboxylate
英文别名
t-Butyl 4-[1-(2-butynyl)-5-cyano-4-hydroxymethyl-1H-imidazol-2-yl]piperazine-1-carboxylate;tert-butyl 4-[1-but-2-ynyl-5-cyano-4-(hydroxymethyl)imidazol-2-yl]piperazine-1-carboxylate
t-Butyl 4-[1-(2-butynyl)-5-cyano-4-hydroxymethyl-1H-imidazol-2-yl] piperazine-1-carboxylate化学式
CAS
635723-38-5
化学式
C18H25N5O3
mdl
——
分子量
359.428
InChiKey
ZWEMEPJPSNHVRA-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):
    1.1
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    94.6
  • 氢给体数:
    1
  • 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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Heteroatom bridged metallocene compounds for olefin polymerization
    申请人:Voskoboynikov Z. Alexander
    公开号:US20070135597A1
    公开(公告)日:2007-06-14
    This invention relates to a transition metal compound represented by the formula: wherein M is a group 3, 4, 5 or 6 transition metal atom, or a lanthanide metal atom, or actinide metal atom; E is: 1) a substituted or unsubstituted indenyl ligand that is bonded to Y through the four, five, six or seven position of the indenyl ring, or 2) a substituted or unsubstituted heteroindenyl ligand that is bonded to Y through the four, five or six position of the heteroindenyl ring, provided that the bonding position is not the same as the position of the ring heteroatom, or 3) a substituted or unsubstituted fluorenyl ligand that is bonded to Y through the one, two, three, four, five, six, seven or eight position of the fluorenyl ring, or 4) a substituted or unsubstituted heterofluorenyl ligand that is bonded to Y through the one, two, three, four, five or six position of the heteroindenyl ring, provided that the bonding position is not the same as the position of the ring heteroatom; A is a substituted or unsubstituted cyclopentadienyl ligand, a substituted or unsubstituted heterocyclopentadienyl ligand, a substituted or unsubstituted indenyl ligand, a substituted or unsubstituted heteroindenyl ligand, a substituted or unsubstituted fluorenyl ligand, a substituted or unsubstituted heterofluorenyl ligand, or other mono-anionic ligand; Y is a Group 15 or 16 bridging heteroatom substituent that is bonded via the heteroatom to E and A; and X are, independently, univalent anionic ligands, or both X are joined and bound to the metal atom to form a metallocycle ring, or both X join to form a chelating ligand, a diene ligand, or an alkylidene ligand. This invention further relates to catalyst systems comprising the above transiotioon metal compounds, activators and optional supports and their use to polymerize or oligomerize olefins.
    本发明涉及一种过渡属化合物,其表示为以下公式:其中M是3、4、5或6族过渡属原子,或属原子,或属原子;E是:1)与Y通过环的四、五、六或七位置结合的取代或未取代的配体,或2)与Y通过杂环环的四、五或六位置结合的取代或未取代的杂环配体,前提是结合位置与环杂原子的位置不同,或3)与Y通过环的一、二、三、四、五、六、七或八位置结合的取代或未取代的配体,或4)与Y通过杂环的一、二、三、四、五或六位置结合的取代或未取代的杂配体,前提是结合位置与环杂原子的位置不同;A是取代或未取代的环戊二烯配体,取代或未取代的杂环戊二烯配体,取代或未取代的配体,取代或未取代的杂环配体,取代或未取代的配体,取代或未取代的杂配体,或其他单阴离子配体;Y是通过杂原子与E和A结合的15族或16族桥接杂原子取代基;X是独立的一价阴离子配体,或两个X结合并与属原子结合形成属环,或两个X结合形成螯合配体、二烯基配体或烷基亚基配体。本发明还涉及包含上述过渡属化合物、活化剂和可选支撑物的催化剂系统及其用于聚合或寡聚烯烃的用途。
  • Combination drug
    申请人:Yasuda Nobuyuki
    公开号:US20060094722A1
    公开(公告)日:2006-05-04
    The present invention provides pharmaceutical agents comprising a dipeptidyl peptidase IV (DPPIV) inhibitor and a biguanide agent in combination, which enhance the effects of active circulating glucagon-like peptide-1 (GLP-1) and/or active circulating glucagon-like peptide-2 (GLP-2).
    本发明提供了一种药物制剂,包括二肽基肽酶IV(DPPIV)抑制剂和双胍类药物的组合,其增强了活性循环胰高血糖素样肽-1(GLP-1)和/或活性循环胰高血糖素样肽-2(GLP-2)的效果。
  • Novel condensed imidazole derivatives
    申请人:Yoshikawa Seiji
    公开号:US20060100199A1
    公开(公告)日:2006-05-11
    The present invention is related to compounds represented by the following formula, or salts or hydrates thereof wherein, T 1 represents a 4- to 12-membered heterocyclic group containing one or two nitrogen atoms in the ring, which is a monocyclic or bicyclic structure that may have one or more substituents; X represents a C 1-6 alkyl group which may have one or more substituents, or such; Z 1 and Z 2 each independently represent a nitrogen atom or a group represented by the formula —CR 2 —; R 1 and R 2 independently represent a hydrogen atom, a C 1-6 alkyl group which may have one or more substituents, or a C 1-6 alkoxy group which may have one or more substituents, or such. These are novel compounds that exhibit an excellent
    本发明涉及以下式子所表示的化合物、盐或合物:其中,T1代表一个含有一个或两个氮原子的4-至12元杂环基团,它是一个单环或双环结构,可能有一个或多个取代基;X代表一个C1-6烷基基团,它可能有一个或多个取代基,或者如此;Z1和Z2各自独立地代表一个氮原子或者由公式—CR2—所表示的基团;R1和R2各自独立地代表一个氢原子,一个C1-6烷基基团,它可能有一个或多个取代基,或者一个C1-6烷氧基基团,它可能有一个或多个取代基,或者如此。这些是新颖的化合物,具有优异的性能。
  • CONDENSED IMIDAZOLE DERIVATIVES
    申请人:Yoshikawa Seiji
    公开号:US20090018331A1
    公开(公告)日:2009-01-15
    The present invention is related to compounds represented by the following formula, or salts or hydrates thereof wherein, T 1 represents a 4- to 12-membered heterocyclic group containing one or two nitrogen atoms in the ring, which is a monocyclic or bicyclic structure that may have one or more substituents; X represents a C 1-6 alkyl group which may have one or more substituents, or such; Z 1 and Z 2 each independently represent a nitrogen atom or a group represented by the formula —CR 2 —; R 1 and R 2 independently represent a hydrogen atom, a C 1-6 alkyl group which may have one or more substituents, or a C 1-6 alkoxy group which may have one or more substituents, or such. These are novel compounds that exhibit an excellent DPPIV-inhibiting activity.
    本发明涉及下式所示的化合物、盐或合物: 其中, T1表示一个4-到12成员的杂环基团,在环中含有一个或两个氮原子,是单环或双环结构,可以有一个或多个取代基; X表示一个C1-6烷基基团,可以有一个或多个取代基; Z1和Z2各自独立地表示一个氮原子或由公式—CR2—表示的基团; R1和R2各自独立地表示氢原子、一个C1-6烷基基团,可以有一个或多个取代基,或一个C1-6烷氧基基团,可以有一个或多个取代基。 这些是具有出色的DPPIV抑制活性的新型化合物。
  • NOVEL FUSED IMIDAZOLE DERIVATIVE
    申请人:Eisai Co., Ltd.
    公开号:EP1514552A1
    公开(公告)日:2005-03-16
    The present invention is related to compounds represented by the following formula, or salts or hydrates thereof wherein, T1 represents a 4- to 12-membered heterocyclic group containing one or two nitrogen atoms in the ring, which is a monocyclic or bicyclic structure that may have one or more substituents; X represents a C1-6 alkyl group which may have one or more substituents, or such; Z1 and Z2 each independently represent a nitrogen atom or a group represented by the formula -CR2-; R1 and R2 independently represent a hydrogen atom, a C1-6 alkyl group which may have one or more substituents, or a C1-6 alkoxy group which may have one or more substituents, or such. These are novel compounds that exhibit an excellent DPPIV-inhibiting activity.
    本发明涉及下式所代表的化合物或其盐类或合物 其中 T1 代表环中含有一个或两个氮原子的 4 至 12 元杂环基团,其为单环或双环结构,可具有一个或多个取代基; X 代表可带有一个或多个取代基的 C1-6 烷基,或此类; Z1和Z2各自独立地代表一个氮原子或一个由式-CR2-代表的基团; R1和R2各自独立地代表氢原子、C1-6烷基(可带有一个或多个取代基)或C1-6烷氧基(可带有一个或多个取代基)或此类基团。 这些新型化合物具有优异的 DPPIV 抑制活性。
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