1,3-二甲基-6-哌嗪-1-基嘧啶-2,4-二酮 | 80210-72-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 中文名称: 1,3-二甲基-6-哌嗪-1-基嘧啶-2,4-二酮
• 英文名称: 1,3-dimethyl-6-(piperazine-1-yl)-2,4(1H,3H)-pyrimidinedione
• 英文别名: 1,3-dimethyl-6-(1-piperazinyl)-2,4(1H,3H)-pyrimidinedione；1,3-dimethyl-6-(piperazin-1-yl)-2,4(1H,3H)-pyrimidinedione；1,3-Dimethyl-6-(piperazin-1-yl)-1,2,3,4-tetrahydropyrimidine-2,4-dione；1,3-dimethyl-6-piperazin-1-ylpyrimidine-2,4-dione
• CAS: 80210-72-6
• 化学式: C₁₀H₁₆N₄O₂
• 分子量: 224.263
• InChiKey: XQQQZORCKOPSMV-UHFFFAOYSA-N

物化性质

• 沸点：
  345.0±52.0 °C(Predicted)
• 密度：
  1.245±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -0.9
• 重原子数：
  16
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  55.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1,3-二甲基-6-哌嗪-1-基嘧啶-2,4-二酮 在 三乙胺 作用下， 以 1,4-二氧六环 、 氯仿 为溶剂， 生成 1,3-dimethyl-6-[4-(3-[3-nitrophenoxy]propyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione
  参考文献：
  名称：

  Pyrimidinedione derivatives and antiarrhythmic agents containing same

  摘要：

  Pyrimidinedione衍生物的化学式为：##STR1## 其中R.sup.1和R.sup.2通过一个烷基链相连，从而形成一个杂环结构，A，R.sup.3，R.sup.4，X.sup.1，X.sup.2和X.sup.3分别是取代基，n为2或3，具有一个基本骨架，其中苯基部分和嘧啶二酮部分通过一个包含一个烷基链和一个含有两个氮原子的杂环环的结构相连。这些化合物对于治疗心律失常很有用。

  公开号：

  US05332739A1

文献信息

• Pyrimidinedione compounds, method of producing the same and
  申请人：Mitsui Toatsu Chemicals, Incorporated

  公开号：US05008267A1

  公开（公告）日：1991-04-16

  A pyrimidinedione derivative compound has a basic backbone in which a phenyl group part and a pyrimidinedione part are linked by a structure comprising an alkyl chain containing at least two nitrogen atoms. The pyrimidinedione derivative is useful for a medical treatment of cardiac arrhythmias.

  一种嘧啶二酮衍生物化合物具有一个基本的骨架，其中苯基部分和嘧啶二酮部分通过含有至少两个氮原子的烷基链连接。这种嘧啶二酮衍生物对治疗心律失常具有医疗用途。
• Synthesis and structure–activity relationships of phenothiazine carboxylic acids having pyrimidine-dione as novel histamine H1 antagonists
  作者：Katsumi Kubota、Hirotaka Kurebayashi、Hirotaka Miyachi、Masanori Tobe、Masako Onishi、Yoshiaki Isobe

  DOI：10.1016/j.bmcl.2009.03.124

  日期：2009.5

  A series of phenothiazine carboxylic acid derivatives, having 6-amino-pyrimidine-2,4(1H,3H)-dione moiety via a appropriate linker, were synthesized and evaluated for their affinity toward human histamine H1 receptor and Caco-2 cell permeability. Selected compounds were further evaluated for their oral anti-histaminic activity in mice and bioavailability in rats. Finally, promising compounds were examined

  合成了一系列通过适当的接头具有6-氨基-嘧啶-2,4（1 H，3 H）-二酮部分的吩噻嗪羧酸衍生物，并评估了它们对人组胺H 1受体和Caco-2的亲和力细胞通透性。进一步评估了所选化合物在小鼠中的口服抗组胺活性和在大鼠中的生物利用度。最后，在小鼠OVA诱导的双相皮肤反应模型中检查了有希望的化合物的抗炎潜力。在所测试的化合物中，吩噻嗪乙酸化合物27在体内模型中均显示出组胺H 1受体拮抗活性和抗炎活性。
• Synthesis and pharmacological studies of N-substituted 6-[(2-aminoethyl)amino]-1,3-dimethyl-2,4(1H,3H)-pyrimidinediones, novel class III antiarrhythmic agents
  作者：Tsutomu Katakami、Tatsuro Yokoyama、Michihiko Miyamoto、Haruki Mori、Nobuya Kawauchi、Tadahito Nobori、Kunio Sannohe、Tatsuo Kaiho、Joji Kamiya

  DOI：10.1021/jm00096a003

  日期：1992.9

  A series of 6-[(2-aminoethyl)amino]-1,3-dimethyl-2,4(1H,3H)- pyrimidinedione derivatives were synthesized and studied for their class III electrophysiological activity and class II (beta-blocking) effects in in vitro and in vivo models. Structure-activity relationships are discussed for a series of compounds. Several members of this series prolonged the action potential duration at 75% repolarization

  合成了一系列6-[[（2-氨基乙基）氨基] -1,3-二甲基-2,4（1H，3H）-嘧啶二酮衍生物，并研究了它们的Ⅲ类电生理活性和Ⅱ类（β-阻断）作用在体外和体内模型中。讨论了一系列化合物的构效关系。该系列的几名成员延长了分离的犬浦肯野纤维重极化75％时的动作电位持续时间，并且其功效比d-索他洛尔高10-30倍。1,3-二甲基-6-[[[2- [N- [3-（4-硝基苯基）丙基] -N-（羟乙基）氨基]乙基]氨基] -2,4-（1H，3H）-嘧啶二酮（ 40），是该系列中最有效的化合物之一。
• Pyrimidinedione derivative compounds, method for preparing same, and
  申请人：Mitsui Toatsu Chemicals, Incorporated

  公开号：US05114941A1

  公开（公告）日：1992-05-19

  A pyrimidinedione derivative compound has a basic backbone in which a 4-oxobenzopyran ring group part and a pyrimidinedione part are linked by a structure comprising an alkyl chain containing at least two nitrogen atoms and one oxygen. The pyrimidinedione derivative is useful for a medical treatment of cardiac arrhythmias.

  一种嘧啶二酮衍生物化合物具有一种基本骨架，其中4-氧基苯并吡喃环团部分和嘧啶二酮部分通过含有至少两个氮原子和一个氧原子的烷基链结合。这种嘧啶二酮衍生物对治疗心律失常具有医疗用途。
• Pyrimidinedione derivatives and antiarrythmic agents containing the same
  申请人：Mitsui Toatsu Chemicals, Incorporated

  公开号：US05308848A1

  公开（公告）日：1994-05-03

  A pyrimidinedione derivative compound has a basic backbone in which a phenyl group part and a pyrimidinedione part are linked by a linking structure comprising an alkyl chain containing two nitrogen atoms. This linking structure is represented by ##STR1## [wherein A is --(CH.sub.2).sub.n --, --CO-- or --O--(CH.sub.2).sub.m --; each of R.sup.1 and R.sup.2 is independently a hydrogen atom or a lower alkyl group which may be substituted by a hydroxyl group, or R.sup.1 and R.sup.2 may be so linked with each other as to make an alkylene chain and thus form a heterocyclic structure; R.sup.5 is a halogen atom, a hydroxyl group, a lower alkyloxycarbonyl group, a lower alkyloxy group which may be substituted by a lower alkyloxy group, or a lower alkyl group which may be substituted by a hydroxyl group, or R.sup.5 may be so linked with R.sup.1 as to make an alkylene chain and thus form a heterocyclic structure; n is 0, 1, 2 or 3 (when R.sup.5 is the hydroxyl group, n.noteq.0); m is 0, 1, 2 or 3; and k is 0, 1, 2 or 3 (however, a compound in which A is --O--(CH.sub.2).sub.m -- and R.sup.5 is the hydroxyl group is excluded from the pyrimidinedione derivative)]. The pyrimidinedione derivative and its acid addition salt are useful for a medical treatment of cardiac arrhythmias.

  一种嘧啶二酮衍生物化合物具有基本的骨架，其中苯基部分和嘧啶二酮部分通过一个含有两个氮原子的烷基链连接结构连接。该连接结构由##STR1##表示[其中A为--(CH.sub.2).sub.n --，--CO--或--O--(CH.sub.2).sub.m --；R.sup.1和R.sup.2各自独立地为氢原子或低级烷基，可以被羟基取代，或R.sup.1和R.sup.2可以相互连接形成烷基链，从而形成杂环结构；R.sup.5为卤素原子、羟基、低级烷氧羰基基、可以被低级烷氧基取代的低级烷氧基，或可以被羟基取代的低级烷基，或R.sup.5可以与R.sup.1相连形成烷基链，从而形成杂环结构；n为0、1、2或3（当R.sup.5为羟基时，n.noteq.0）；m为0、1、2或3；k为0、1、2或3（但是，其中A为--O--(CH.sub.2).sub.m --且R.sup.5为羟基的化合物被排除在嘧啶二酮衍生物之外)].该嘧啶二酮衍生物及其酸加成盐对心律失常的医疗治疗有用。