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

(+/-)-1-(6-methyl[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl cyclobutylcarbamate | 1170668-41-3

中文名称
——
中文别名
——
英文名称
(+/-)-1-(6-methyl[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl cyclobutylcarbamate
英文别名
1-(6-methyl-[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl N-cyclobutylcarbamate
(+/-)-1-(6-methyl[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl cyclobutylcarbamate化学式
CAS
1170668-41-3
化学式
C12H16N4O2S
mdl
——
分子量
280.351
InChiKey
QRYOASZHTWCCCA-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    96.8
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    1-(6-甲基[1,3]噻唑并[3,2-B] [1,2,4]三唑-5-基)乙醇环丁基胺盐酸盐N,N'-羰基二咪唑二氯甲烷 为溶剂, 反应 0.66h, 以25%的产率得到(+/-)-1-(6-methyl[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl cyclobutylcarbamate
    参考文献:
    名称:
    [EN] USE OF THIAZOLOIMIDAZOLES, THIAZOLOTETRAZOLES AND THIAZOLOTRIAZOLES AS MGLUR5 ANTAGONISTS
    [FR] UTILISATION DE THIAZOLOIMIDAZOLES, DE THIAZOLOTÉTRAZOLES ET DE THIAZOLOTRIAZOLES COMME ANTAGONISTES DE MGLUR5
    摘要:
    该发明涉及在治疗对mGluR5受体拮抗有益的疾病和症状,特别是物质相关障碍中使用式(I)的噻唑三唑,噻唑咪唑和噻唑四唑衍生物。该发明还涉及某些新颖的衍生物。此外,该发明涉及含有这些衍生物的组合物以及它们的制备方法。
    公开号:
    WO2009087220A1
点击查看最新优质反应信息

文献信息

  • [EN] USE OF THIAZOLOIMIDAZOLES, THIAZOLOTETRAZOLES AND THIAZOLOTRIAZOLES AS MGLUR5 ANTAGONISTS<br/>[FR] UTILISATION DE THIAZOLOIMIDAZOLES, DE THIAZOLOTÉTRAZOLES ET DE THIAZOLOTRIAZOLES COMME ANTAGONISTES DE MGLUR5
    申请人:GLAXO GROUP LTD
    公开号:WO2009087220A1
    公开(公告)日:2009-07-16
    The invention relates to the use of thiazolotriazole, thiazoloimidazole and thiazolotetrazole derivatives of formula (I) in treating diseases and conditions for which antagonism of the mGluR5 receptor is beneficial, in particular substance related disorders. The invention also relates to certain novel derivatives. In addition, the invention relates to compositions containing the derivatives and processes for their preparation.
    该发明涉及在治疗对mGluR5受体拮抗有益的疾病和症状,特别是物质相关障碍中使用式(I)的噻唑三唑,噻唑咪唑和噻唑四唑衍生物。该发明还涉及某些新颖的衍生物。此外,该发明涉及含有这些衍生物的组合物以及它们的制备方法。
查看更多

同类化合物

5-(4-甲基苯基)噻唑并[2,3-c]-1,2,4-三唑-3(2H)-硫酮 5-(4-氯苯基)-噻唑并[2,3-c]-1,2,4-三唑-3(2H)-硫酮 1-(6-甲基噻唑并[3,2-B][1,2,4]三唑-5-基)乙酮 1-(6-甲基[1,3]噻唑并[3,2-B] [1,2,4]三唑-5-基)乙醇 5-(4-bromophenyl)-6-methylthiazolo[3,2-b][1,2,4]triazole 6-methyl-5-m-tolylthiazolo[3,2-b][1,2,4]triazole 6-methyl-5-o-tolylthiazolo[3,2-b][1,2,4]triazole (Z)-5-(4-(diethylamino)benzylidene)thiazolo[3,2-b][1,2,4]triazol-6(5H)-one (Z)-5-(furan-2-ylmethylene)thiazolo[3,2-b][1,2,4]triazol-6(5H)-one (Z)-5-(2-fluorobenzylidene)thiazolo[3,2-b][1,2,4]triazol-6(5H)-one (Z)-5-(3,4-dimethoxybenzylidene)thiazolo[3,2-b][1,2,4]triazol-6(5H)-one (Z)-5-(thiophen-2-y-lmethylene)thiazolo[3,2-b][1,2,4]triazol-6(5H)-one (Z)-5-(2-(allyloxy)benzylidene)thiazolo[3,2-b][1,2,4]triazol-6(5H)-one 5-(p-bromophenyl)-3-(2-thienyl)thiazolo[2,3-c]-s-triazole (Z)-5-(2-methoxybenzylidene)thiazolo[3,2-b][1,2,4]triazol-6(5H)-one 3-ethoxycarbonyl-6-methylthiazolo<3,2-c><1,2,3>triazole 6-((4-Chlorophenyl)methylene)-3-methylthiazolo(2,3-c)-1,2,4-triazol-5(6H)-one 6-((4-(Dimethylamino)phenyl)methylene)-3-methylthiazolo(2,3-c)-1,2,4-triazol-5(6H)-one 6-((4-Methoxyphenyl)methylene)-3-methylthiazolo(2,3-c)-1,2,4-triazol-5(6H)-one 6-((4-(Dimethylamino)phenyl)methylene)thiazolo(2,3-c)-1,2,4-triazol-5(6H)-one N-(6-methyl-thiazolo[3,2-b][1,2,4]triazol-2-yl)-diacetamide 5-(4-chlorophenyl)-6-methylthiazolo[3,2-b][1,2,4]triazole (6-methyl[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)methanol 5-phenyl-thiazolo[2,3-c][1,2,4]triazol-3-ylamine 3-ethyl-5-phenylthiazolo[2,3-c][1,2,4]triazole <2-Ethoxy-2-(6-methylthiazolo<3,2-b><1,2,4>triazol-5-yl)ethyl>phosphonsaeure-diethylester <(E)-2-(6-Methylthiazolo<3,2-b><1,2,4>triazol-5-yl)ethenyl>phosphonsaeure-diethylester 5-(3-methoxyphenyl)-6-methylthiazolo[3,2-b]-1,2,4-triazole 5-(3-methoxyphenyl)-6-(p-tolyl)thiazolo[3,2-b][1,2,4]triazole 5-(3-methoxyphenyl)-6-(4-methoxyphenyl)thiazolo[3,2-b][1,2,4]triazole 6-Trimethylsilyltriazolothiazole 2-benzyl-6-[phenyl(piperidin-1-yl)methyl]thiazolo[3,2-b][1,2,4]triazol-5-ol (E)-2-benzyl-6-benzylidenethiazolo[3,2-b][1,2,4]triazol-5(6H)-one 6-((4-(Diethylamino)phenyl)methylene)-3-methylthiazolo(2,3-c)-1,2,4-triazol-5(6H)-one 6-Benzylidenethiazolo[2,3-c][1,2,4]triazol-5(6H)-one 6-methylthiazolo<2,3-c><1,2,3>triazole 1-[6-Methyl-2-(trifluoromethyl)-[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl]ethanone 6-(4-bromophenyl)-5-(3-fluorophenyl)thiazolo[3,2-b]-1,2,4-triazole 5-(3-fluorophenyl)-6-methylthiazolo[3,2-b]-1,2,4-triazole 5-(3-fluorophenyl)-6-p-tolylthiazolo[3,2-b]-1,2,4-triazole 6-[1-Phenyl-meth-(Z)-ylidene]-thiazolo[2,3-c][1,2,4]triazol-5-one N,N-bis([1,3]thiazolo[3,2-b][1,2,4]triazol-6-ylmethyl)cyclohexanamine;hydron;chloride 6-(1H-imidazol-3-ium-3-ylmethyl)-[1,3]thiazolo[3,2-b][1,2,4]triazole;chloride 3-methylsulfanyl-5-phenylthiazolo[2,3-c][1,2,4]triazole 5-[(2,4-Dichlorophenyl)methylidene]-2-(furan-2-yl)[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one 5-[(4-Bromophenyl)methylidene]-2-[2-(4-chlorophenyl)ethenyl][1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one 2-[2-(4-Chlorophenyl)ethenyl]-5-[(5-methylfuran-2-yl)methylidene][1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one 2-[2-(4-Chlorophenyl)ethenyl]-5-{[4-(hexyloxy)-3-methoxyphenyl]methylidene}[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one (+/-)-1-(6-methyl[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)ethyl cyclobutylcarbamate [1,3]Thiazolo[3,2-b][1,2,4]triazole