1-methyl-3-propyl-1H-pyrazole | 41818-31-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 1-methyl-3-propyl-1H-pyrazole
• 英文别名: 1-methyl-3-propylpyrazole
• CAS: 41818-31-9
• 化学式: C₇H₁₂N₂
• 分子量: 124.186
• InChiKey: FKQIJYOUPCNXPZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  9
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  17.8
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  1-chlorohex-1-en-3-one dimethylhydrazone 在 溶剂黄146 作用下， 以 甲醇 为溶剂， 以62%的产率得到1-methyl-3-propyl-1H-pyrazole
  参考文献：
  名称：

  1-Alkylpyrazoles and 1-alkyl-5-chloropyrazoles from halovinyl ketones and 1,1-dialkylhydrazines

  摘要：

  Regioselective heterocyclization of alkyl 2-chloro- and 2,2-dichlorovinyl ketones with 1,1-dialkylhydrazines to 1,3-dialkyl-1H-pyrazoles and 1,3-dialkyl-5-chloro-1H-pyrizoles involves intermediate formation of the corresponding dialkylhydrazones. Fragmentation pattern of chlorine-containing pyrazoles, 3-chloromethyl-1-methyl-1H-pyrazole and 5-chloro-1-methyl-3-propyl-1H-pyrazole, depends on the position of the halogen atom.

  DOI：

  10.1134/s1070428008080150

文献信息

• NITROGEN-CONTAINING HETEROCYCLIC COMPOUND OR SALT THEREOF
  申请人：FUJIFILM Corporation

  公开号：US20150322063A1

  公开（公告）日：2015-11-12

  A compound represented by Formula [1] (in the formula, Z 1 represents N, CH, or the like; X 1 represents NH or the like; R 1 represents a heteroaryl group or the like; each of R 2 , R 3 , and R 4 represents a hydrogen atom, a halogen atom, an alkoxy group, or the like; and R 5 represents a heteroaryl group or the like) or salt thereof.

  由式[1]表示的化合物（在该式中，Z表示N、CH或类似物；X表示NH或类似物；R表示杂环烷基或类似物；R2、R3和R4中的每一个表示氢原子、卤原子、烷氧基或类似物；R5表示杂环烷基或类似物）或其盐。
• [EN] PIKFYVE KINASE INHIBITORS<br/>[FR] INHIBITEURS DE KINASE PIKFYVE
  申请人：ACURASTEM INCORPORATED

  公开号：WO2021163727A1

  公开（公告）日：2021-08-19

  The present invention relates to compounds useful as inhibitors of phosphatidylinositol-3-phosphate 5-kinase (PIKfyve) as well as their use for treating diseases and disorders associated with PIKfyve.

  本发明涉及作为磷脂酰肌醇-3-磷酸5-激酶（PIKfyve）抑制剂的化合物，以及它们用于治疗与PIKfyve相关的疾病和紊乱的用途。
• HIGHLY SELECTIVE and LONG-ACTING PDE5 MODULATORS
  申请人：Gant Thomas G.

  公开号：US20080194529A1

  公开（公告）日：2008-08-14

  Disclosed herein are substituted phosphodiesterase type 5 enzyme modulators of Formula I, processes of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.

  披露的是式I的取代的磷酸二酯酶5型酶调节剂，其制备过程，药物组合物及其用途。
• [EN] 2,3,5-TRISUBSTITUTED PYRAZOLO[1,5-A]PYRIMIDINE COMPOUNDS<br/>[FR] COMPOSÉS DE PYRAZOLO[1,5-A]PYRIMIDINE 2,3,5-TRISUBSTITUÉS
  申请人：ARCUS BIOSCIENCES INC

  公开号：WO2020247496A1

  公开（公告）日：2020-12-10

  Compounds that inhibit PI3Kγ, and compositions containing the compound(s) and methods for synthesizing the compounds, are described herein. Also described are the use of such compounds and compositions for the treatment of a diverse array of diseases, disorders, and conditions, including cancer- and immune-related disorders that are mediated, at least in part, by PI3Kγ.

  本文描述了抑制PI3Kγ的化合物，以及含有该化合物的组合物和合成该化合物的方法。还描述了利用这些化合物和组合物治疗各种疾病、疾病和疾病的用途，包括至少部分由PI3Kγ介导的癌症和免疫相关疾病。
• PYRROLO[2,3-d]PYRIMIDINE TROPOMYSIN-RELATED KINASE INHIBITORS
  申请人：Andrews Mark David

  公开号：US20120258950A1

  公开（公告）日：2012-10-11

  The present invention relates to compounds of Formula (I) and their pharmaceutically acceptable salts, wherein the substituents are as described herein, and their use in medicine, in particular as Trk antagonists.

  本发明涉及式(I)化合物及其药学上可接受的盐，其中取代基如本文所述，并且它们在医学上的用途，特别是作为Trk拮抗剂。