5-methyl-pyrazine-2-carbonyl azide | 457098-83-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 5-methyl-pyrazine-2-carbonyl azide
• 英文别名: 5-methyl-pyrazin-2-carbonyl azide；5-methylpyrazine-2-carboxylic azide；5-methylpyrazine-2-carbonyl azide
• CAS: 457098-83-8
• 化学式: C₆H₅N₅O
• 分子量: 163.139
• InChiKey: JSXYKMRDXPBXRD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  57.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  5-methyl-pyrazine-2-carbonyl azide 以 1,4-二氧六环 、 甲苯 为溶剂， 反应 25.0h， 生成 cis-1-(2-methoxy-6-oxo-1,2,3,4,6,10b-hexahydropyrido[2,1-a]isoindol-10-yl)-3-(5-methylpyrazin-2-yl)urea
  参考文献：
  名称：

  Advances in tetrahydropyrido[1,2- a ]isoindolone (valmerins) series: Potent glycogen synthase kinase 3 and cyclin dependent kinase 5 inhibitors

  摘要：

  An efficient synthetic strategy was developed to modulate the structure of the tetrahydropyridine iso-indolone (Valmerin) skeleton. A library of more than 30 novel final structures was generated. Biological activities on CDK5 and GSM as well as cellular effects on cancer cell lines were measured for each novel compound. Additionally docking studies were performed to support medicinal chemistry efforts. A strong GSK3/CDK5 dual inhibitor (38, IC50 GSK3/CDK5 32/84 nM) was obtained. A set of highly selective GSK3 inhibitors was synthesized by fine-tuning structural modifications (29 IC50 GSK3/CDK5 32/320 nM). Antiproliferative effects on cells were correlated with the in vitro Kinase activities and the best effects were obtained with lung and colon cell lines. (C) 2015 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2015.06.046
• 作为产物：
  描述：

  5-甲基吡嗪-2-羧酸 在 叠氮磷酸二苯酯 、 N,N-二异丙基乙胺 作用下， 以 甲苯 为溶剂， 反应 2.0h， 生成 5-methyl-pyrazine-2-carbonyl azide
  参考文献：
  名称：

  使用Curtius重排作为吡嗪构建基团的多千克生产的一部分

  摘要：

  葡萄糖激酶激活剂的商业路线定义要求重新评估用于获取多千克量的2-氨基-5-甲基吡嗪的合成和工艺。在考虑了不同的选择之后，选择了用于药物化学路线的库尔修斯重排的变化形式，以进行进一步的开发。库尔修斯重排的酰基叠氮化物的形成需要采取过程安全控制策略。从5-甲基吡嗪-2-羧酸开始，开发的工艺用于成功交付总重量达68％的多千克量的2-氨基-5-甲基吡嗪。

  DOI：

  10.1021/acs.oprd.7b00340

文献信息

• Compounds useful for inhibiting Chk1
  申请人：——

  公开号：US20030069284A1

  公开（公告）日：2003-04-10

  Aryl- and heteroaryl-substituted urea compounds useful in the treatment of diseases and conditions related to DNA damage or lesions in DNA replication are disclosed. Methods of making the compounds, and their use as therapeutic agents, for example, in treating cancer and other diseases characterized by defects in DNA replication, chromosome segregation, or cell division also are disclosed.

  公开了芳基和杂芳基取代脲化合物，用于治疗与DNA损伤或DNA复制中DNA损伤有关的疾病和状况。还公开了制造这些化合物的方法，以及它们作为治疗剂的使用，例如，在治疗由DNA复制、染色体分离或细胞分裂缺陷引起的癌症和其他疾病。
• Substituted-cycloalkyl and oxygenated-cycloalkyl glucokinase activators
  申请人：——

  公开号：US20030225283A1

  公开（公告）日：2003-12-04

  2,3-Di-substituted N-heteroaromatic propionamides with said substitution at the 2-position being a substituted phenyl group and at the 3-position being a polar ring, said propionamides being glucokinase activators which increase insulin secretion in the treatment of type II diabetes.

  2,3-二取代N-杂环丙酰胺，其中2-位置的取代物是取代苯基，3-位置的取代物是极性环，这些丙酰胺是葡萄糖激酶激活剂，可增加胰岛素分泌，用于治疗2型糖尿病。
• [EN] BISARYLUREA DERIVATIVES USEFUL FOR INHIBITING CHK1<br/>[FR] DÉRIVÉS DE BISARYLURÉE UTILES POUR INHIBER CHK1
  申请人：ICOS CORP

  公开号：WO2006012308A1

  公开（公告）日：2006-02-02

  Aryl- and heteroaryl-substituted urea compounds useful in the treatment of diseases and conditions related to DNA damage or lesions in DNA replication are disclosed. Methods of making the compounds, and their use as therapeutic agents, for example, in treating cancer and other diseases characterized by defects in DNA replication, chromosome segregation, or cell division also are disclosed. Formula (I).

  披苯基和杂环基取代的脲化合物可用于治疗与DNA损伤或DNA复制中的损伤相关的疾病和病况。公开了制备这些化合物的方法，以及它们作为治疗剂的用途，例如在治疗癌症和其他以DNA复制缺陷、染色体分离或细胞分裂为特征的疾病中的应用。公式（I）。
• [EN] SUBSTITUTED PHENYLACETAMIDES AND THEIR USE AS GLUCOKINASE ACTIVATORS<br/>[FR] ACTIVATEURS DE GLUCOKINASE OXYGENES CYCLOALKYLE OU SUBSTITUES CYCLOALKYLE
  申请人：HOFFMANN LA ROCHE

  公开号：WO2003095438A1

  公开（公告）日：2003-11-20

  Compounds of the formula (I); wherein formula (II) represents a substituted group, an oxa-cycloalkyl group or a thia-cycloalkyl group, are glucokinase activators useful in the treatment of type II diabetes.

  式(I)的化合物；其中式(II)代表取代基团，氧杂环烷基团或硫杂环烷基团，是一种在治疗II型糖尿病中有用的葡萄糖激酶激活剂。
• [EN] ARYL AND HETEROARYL UREA CHK1 INHIBITORS FOR USE AS RADIOSENSITIZERS AND CHAMOSENSITIZERS<br/>[FR] UREE ARYLE ET HETEROARYLE UTILISEE EN TANT QU'INHIBITEUR DE CHK1, A UTILISER EN TANT QUE RADIOSENSIBILISANTS ET CHIMIOSENSIBILISANTS
  申请人：ICOS CORP

  公开号：WO2002070494A1

  公开（公告）日：2002-09-12

  Aryl- and heteroaryl substituted urea compounds useful in the treatment of diseases and conditions related to DNA damage or lesions in DNA replication are disclosed. Methods of making the compounds, and their use as therapeutic agents, for example, in treating cancer and other diseases characterized by defects in DNA replication, chromosome segregation, or cell division also are disclosed. Wherein W' is a six-membered aromatic ring containing at least 2 introgen atoms and optionally substitutedas defined in the claims, Z' is a five- or six membered aromatic or heteraromatic ring as defined in the claims, Y' is O or S.

  本发明涉及芳基和杂芳基取代的脲类化合物，用于治疗与DNA损伤或DNA复制中的损伤有关的疾病和病况。本发明还公开了制备这些化合物的方法以及它们作为治疗剂的用途，例如治疗癌症和其他以DNA复制缺陷、染色体分离或细胞分裂为特征的疾病。其中W'是一个含有至少2个氮原子的六元芳环，也可以是根据权利要求中定义的取代基；Z'是根据权利要求中定义的五元或六元芳香环或杂芳香环；Y'是O或S。