摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-甲基-1H-噻吩并[2,3-d]咪唑-2(3h)-酮 | 231630-13-0

中文名称
3-甲基-1H-噻吩并[2,3-d]咪唑-2(3h)-酮
中文别名
——
英文名称
3-methyl-2,3-dihydro-1H-thieno[2,3-d]imidazol-2-one
英文别名
3-Methyl-1H-thieno[2,3-d]imidazol-2(3H)-one;3-methyl-1H-thieno[2,3-d]imidazol-2-one
3-甲基-1H-噻吩并[2,3-d]咪唑-2(3h)-酮化学式
CAS
231630-13-0
化学式
C6H6N2OS
mdl
——
分子量
154.192
InChiKey
CZLSEXFVHQKUKI-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

物化性质

  • 密度:
    1.381±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    60.6
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2934999090

反应信息

  • 作为产物:
    描述:
    2-methylaminothiophene-3-carbonylazide 以 甲苯 为溶剂, 反应 5.0h, 以84%的产率得到3-甲基-1H-噻吩并[2,3-d]咪唑-2(3h)-酮
    参考文献:
    名称:
    Efficient synthesis of N1- or N3-substituted thieno[2,3-d]imidazol-2-ones
    摘要:
    N-1- or N-3-substituted thieno[2,3-d]imidazol-2-one derivatives are selectively obtained after N-alkylation of thiaisatoic anhydrides followed by formation of the N-substituted aminocarbonyl azides and Curtius rearrangement, (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(99)00285-9
点击查看最新优质反应信息

文献信息

  • [EN] THIAZOLE DERIVATIVES AS PROTEIN KINASE INHIBITORS<br/>[FR] DÉRIVÉS DE THIAZOLE ET LEURS PROCÉDÉS D'UTILISATION
    申请人:SCHERING CORP
    公开号:WO2009058728A1
    公开(公告)日:2009-05-07
    The present invention relates to novel Thiazole Derivatives, compositions comprising the Thiazole Derivatives, and methods for using the Thiazole Derivatives for treating or preventing a proliferative disorder, an anti-proliferative disorder, inflammation, arthritis, a central nervous system disorder, a cardiovascular disease, alopecia, a neuronal disease, an ischemic injury, a viral infection, a fungal infection, or a disorder related to the activity of a protein kinase.
    本发明涉及新型噻唑衍生物,包含该噻唑衍生物的组合物,以及使用该噻唑衍生物治疗或预防增生性疾病、抗增生性疾病、炎症、关节炎、中枢神经系统疾病、心血管疾病、脱发、神经疾病、缺血性损伤、病毒感染、真菌感染或与蛋白激酶活性相关的疾病的方法。
  • [EN] TRPA1 MODULATORS<br/>[FR] MODULATEURS DE TRPA1
    申请人:ALGOMEDIX INC
    公开号:WO2015103060A1
    公开(公告)日:2015-07-09
    This disclosure relates to polycyclic heteroaromatic compounds useful as TRPA1 modulators, as well as compositions and methods of treating pain that include the compounds.
    这份披露涉及到多环杂芳化合物,这些化合物可用作TRPA1调节剂,以及包括这些化合物的用于治疗疼痛的组合物和方法。
  • Thiazole Derivatives as Protein Kinase Inhibitors
    申请人:Reddy Panduranga Adulla P.
    公开号:US20100331313A1
    公开(公告)日:2010-12-30
    The present invention relates to novel Thiazole Derivatives, compositions comprising the Thiazole Derivatives, and methods for using the Thiazole Derivatives for treating or preventing a proliferative disorder, an anti-proliferative disorder, inflammation, arthritis, a central nervous system disorder, a cardiovascular disease, alopecia, a neuronal disease, an ischemic injury, a viral infection, a fungal infection, or a disorder related to the activity of a protein kinase.
  • TRPA1 MODULATORS
    申请人:Algomedix, Inc.
    公开号:US20170001983A1
    公开(公告)日:2017-01-05
    This disclosure relates to polycyclic heteroaromatic compounds useful as TRPA1 modulators, as well as compositions and methods of treating pain that include the compounds.
  • US8476278B2
    申请人:——
    公开号:US8476278B2
    公开(公告)日:2013-07-02
查看更多

同类化合物

沙维拉唑 4H-吡咯并[1,2-a]噻吩并[3,2-D]咪唑 3H-噻吩并[2,3-d]咪唑-5-羧酸 3-甲基-1H-噻吩并[2,3-d]咪唑-2(3h)-酮 2-(氯甲基)-1H-噻吩并[3,4-d]咪唑 1H-噻吩并[3,2-D]咪唑-2(3H)-酮 1H-噻吩并[2,3-d]咪唑,1-乙烯基-(9CI) 1H-噻吩并(3,4-d)咪唑,2-(((5-甲基-2-吡啶基)甲基)亚硫酰基)- 1-甲基-1H-噻吩并[2,3-D]咪唑基-2(3H)-酮 1-乙烯基-1H-噻吩并[2,3-d]咪唑-5-羧酸 1,3-二氢噻吩并[3,4-d]咪唑-2-硫酮 tert-butyl 4-[4-(2,3-dihydro-2-oxo-1-tert-butoxycarbonyl-1H-thieno[3,4-d]imidazol-4-yl)phenyl]-2,3-dihydro-2-oxo-1H-thieno[3,4-d]imidazole-1-carboxylate 2-(3-Bromo-4-methoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-[3-Methoxy-4-(2,2,2-trifluoro-ethoxy)-pyridin-2-ylmethylsulfanyl]-1H-thieno[3,4-d]imidazole 2-(2-diethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazole 2-(5-Bromo-4-methoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-(5-Chloro-4-methoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole 2-(2-dimethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazole 6-amino-1-vinylthieno[2,3-d]imidazole-5-carboxamide 1-Vinyl-1H-thieno[2,3-d]imidazole-5-carboxylic acid ethyl ester 2-(3-Chloro-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole 2-(5-Methoxy-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole (2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-thieno[2,3-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate 1-methyl-2-methoxymethyl-thieno[2.3-d]imidazol-5-yl-carboxylic acid 2-(3-Fluoro-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole 2-(4-Benzyloxy-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole 2-(4-methoxy-2-picolylsulfinyl)-1H-thieno[3,4-d]imidazole 2-[(4-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[2,3-d]imidazole 4-(4-methoxyphenyl)-2-[(4-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-(4-methoxy-2-picolylmercapto)-1H-thieno[3,4-d]imidazole methyl 2-[(4-methoxypyridin-2-yl)methylsulfanyl]-1H-thieno[3,4-d]imidazole-4-carboxylate 2-[(4-methoxypyridin-2-yl)methylsulfinyl]-4-phenyl-1H-thieno[3,4-d]imidazole dimethyl 2-[(4-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[2,3-d]imidazole-5,6-dicarboxylate 2-[(4-methoxypyridin-2-yl)methylsulfanyl]-1H-thieno[2,3-d]imidazole methyl 2-[(4-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole-4-carboxylate 1-Ethoxycarbonyl-2-(4-methoxy-2-picolylsulfinyl)-1H-thieno[3,4-d]imidazole 1-ethoxycarbonyl-2-(4-methoxy-2-picolylmercapto)-1H-thieno[3,4-d]imidazole ethyl 2-methylthieno[2,3-d]imidazol-5-carboxylate 2-[(5-chloropyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-[(4-Thiazolyl)methylthio]thieno[3,4-d]imidazole 2-[[3-Methoxy-4-(2,2,3,3,4,4,4-heptafluorobutoxy)-2-pyridinyl]methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-[(3-methoxypyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-[(3,4-dimethoxypyridin-2-yl)methylsulfanyl]-1H-thieno[3,4-d]imidazole 2-[(3,4-dimethoxypyridin-2-yl)methylsulfinyl]-1H-thieno[3,4-d]imidazole 2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]-4-(4-methoxyphenyl)-1H-thieno[3,4-d]imidazole 2-(4-methoxy-3,5-dimethyl-2-picolylsulfinyl)-1H-thieno[3,4-d]imidazole 2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]-4-phenyl-1H-thieno[3,4-d]imidazole 2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfanyl]-1H-thieno[3,4-d]imidazole (3S,3'S,5S,5'S)-tert-butyl 5,5'-(5,5'-(buta-1,3-diyne-1,4-diyl)bis(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-thieno[2,3-d]imidazole-5,2-diyl))bis(3-methylpyrrolidine-1-carboxylate) (2S,4S)-tert-butyl 2-(5-ethynyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-thieno[2,3-d]imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate