N-(2-氰乙基)-N-甲基乙酰胺 | 4271-90-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: N-(2-氰乙基)-N-甲基乙酰胺
• 中文别名: N-乙酰基-N-甲基-3-氨基丙腈；N-(2-氰基乙基)-n-甲基乙酰胺
• 英文名称: N-Methyl-N-(β-cyanethyl)-acetamid
• 英文别名: N-(2-cyanoethyl)-N-methylacetamide
• CAS: 4271-90-3
• 化学式: C₆H₁₀N₂O
• mdl: MFCD01598837
• 分子量: 126.158
• InChiKey: XVWNWBDQUDOFRY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.6
• 重原子数：
  9
• 可旋转键数：
  2
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.666
• 拓扑面积：
  44.1
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2926909090

制备方法与用途

用途：噻嘧啶的中间体。

反应信息

• 作为反应物：
  描述：

  1,1,2,2-四氯乙烷 、 N-(2-氰乙基)-N-甲基乙酰胺 、 光气 、 五氯化磷 、 三氯氧磷 、 氯 生成 4,5-dichloro-2-(trichloromethyl)pyrimidine
  参考文献：
  名称：

  BECK, G.;HEITZER, H.

  摘要：

  DOI：

文献信息

• Bicyclic pyrrolyl amides as glucogen phosphorylase inhibitors
  申请人：——

  公开号：US20030232875A1

  公开（公告）日：2003-12-18

  Heterocyclic amide derivatives, of formula (I): wherein —X-Y-Z- is selected from —S—CR 4 ═CR 5 —, —CR 4 ═CR 5 —S—, —O—CR 4 ═CR 5 —, —CR 4 ═CR 5 —O—, —N═CR 4 —S—, —S—CR 4 ═N—, —NR 6 —CR 4 ═CR 5 — and —CR 4 ═CR 5 —NR 6 —; or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof; (with provisos); possess glycogen phosphorylase inhibitory activity and accordingly have value in the treatment of disease states associated with increased glycogen phosphorylase activity. Processes for the manufacture of said heterocyclic amide derivatives and pharmaceutical compositions containing them are described.

  杂环酰胺衍生物的化学式（I）：其中—X-Y-Z-选择自—S—CR4═CR5—，—CR4═CR5—S—，—O—CR4═CR5—，—CR4═CR5—O—，—N═CR4—S—，—S—CR4═N—，—NR6—CR4═CR5—和—CR4═CR5—NR6—；或其药学上可接受的盐或体内可水解酯；（附带条件）；具有糖原磷酸化酶抑制活性，因此在治疗与糖原磷酸化酶活性增加相关的疾病状态中具有价值。描述了制备所述杂环酰胺衍生物和含有它们的药物组合物的方法。
• FUSED RING HETEROCYCLE KINASE MODULATORS
  申请人：Chen Chixu

  公开号：US20080261921A1

  公开（公告）日：2008-10-23

  The present invention provides fused ring heterocycles as kinase modulators, pharmaceutical compositions containing these modulators, and methods of using these modulators to treat diseases mediated by kinase activity.

  本发明提供了融合环杂环化合物作为激酶调节剂，含有这些调节剂的药物组合物，以及使用这些调节剂治疗由激酶活性介导的疾病的方法。
• Fused heterocycle derivative
  申请人：Sawada Takashi

  公开号：US20090239853A1

  公开（公告）日：2009-09-24

  A fused heterocycle derivative represented by the general formula (I): (wherein R 1 represents optionally substituted lower alkyl, or the like; R 2 represents an optionally substituted aliphatic heterocyclic group, or the like; R 3 represents —C(=Z)NR 5 R 6 (wherein R 5 and R 6 represent optionally substituted lower alkyl, or the like, and Z represents an oxygen atom or the like), or the like; n represents an integer of 1 to 3; and W represents C—R 5 (wherein R 5 represents a hydrogen atom or the like)) or a pharmaceutically acceptable salt thereof, and the like are provided.

  提供一种由通式（I）表示的融合杂环衍生物：（其中R1代表可选取代的低碳基等；R2代表可选取代的脂肪族杂环基等；R3代表—C（=Z）NR5R6（其中R5和R6代表可选取代的低碳基等，Z代表氧原子等）等；n代表1到3的整数；W代表C—R5（其中R5代表氢原子等）或类似物的药物可接受的盐等。
• 5-PHENYLTHIAZOLE DERIVATIVES AND USE AS PI3 KINASE INHIBITORS
  申请人：Bruce Ian

  公开号：US20100093690A1

  公开（公告）日：2010-04-15

  Compounds of formula I in free or salt form, wherein R 1 , R 2 , R 3 , R 4 and R 5 have the meanings as indicated in the specification, are useful for treating diseases mediated by phosphatidylinositol 3-kinase. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.

  式I的化合物，无论是自由形式还是盐形式，其中R1、R2、R3、R4和R5的含义如规范中所示，对于治疗由磷脂酰肌醇3-激酶介导的疾病是有用的。还描述了含有这些化合物的制药组合物以及制备这些化合物的过程。
• PYRIDO[3,2-d]PYRIMIDINE PI3K DELTA INHIBITOR COMPOUNDS AND METHODS OF USE
  申请人：Genentech, Inc.

  公开号：US20130225557A1

  公开（公告）日：2013-08-29

  Formula I compounds, including stereoisomers, geometric isomers, tautomers, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting the delta isoform of PI3K, and for treating disorders mediated by lipid kinases such as inflammation, immunological disorders, and cancer. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

  公式I化合物包括立体异构体、几何异构体、互变异构体、代谢产物和药学上可接受的盐，可用于抑制PI3K的δ异构体，并用于治疗由脂质激酶介导的炎症、免疫性疾病和癌症等疾病。揭示了使用公式I化合物进行哺乳动物细胞中的体外、原位和体内诊断、预防或治疗此类疾病或相关病理条件的方法。