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4-(6-methylthiazolo[3,2-b][1,2,4]triazol-5-yl)-N-phenylthiazol-2-amine

中文名称
——
中文别名
——
英文名称
4-(6-methylthiazolo[3,2-b][1,2,4]triazol-5-yl)-N-phenylthiazol-2-amine
英文别名
N-[4-(6-methyl[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)-1,3-thiazol-2-yl]-N-phenylamine;4-(6-methyl-[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)-N-phenyl-1,3-thiazol-2-amine
4-(6-methylthiazolo[3,2-b][1,2,4]triazol-5-yl)-N-phenylthiazol-2-amine化学式
CAS
——
化学式
C14H11N5S2
mdl
——
分子量
313.407
InChiKey
HGHOATCIRMWENE-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):
    3.9
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    112
  • 氢给体数:
    1
  • 氢受体数:
    6

文献信息

  • Thiazole compounds and methods of use
    申请人:Zhang Suoming
    公开号:US20070004711A1
    公开(公告)日:2007-01-04
    The present invention provides compounds, salts and hydrates of Formula I, wherein the variables Ar 1 , R 2 , R 3 , R 4 , r, q, and t are defined herein. Certain compounds of Formula I described herein possess potent antiviral activity. The invention also provides compounds of Formula I that are potent and/or selective inhibitors of Hepatitis C virus replication. Certain compounds described herein inhibit assembly of the HCV replication complex. The invention also provides pharmaceutical compositions containing one or more compounds of Formula I, or a salt, solvate, or acylated prodrug of such compounds, and one or more pharmaceutically acceptable carriers, excipients, or diluents. The invention further comprises methods of treating patients suffering from certain infectious diseases by administering to such patients an amount of a compound of Formula I effective to reduce signs or symptoms of the disease. These infectious diseases include viral infections, particularly HCV infections. The invention is particularly includes methods of treating human patients suffering from an infectious disease, but also encompasses methods of treating other animals, including livestock and domesticated companion animals, suffering from an infectious disease. Methods of treatment include administering a compound of Formula I as a single active agent or administering a compound of Formula I in combination with on or more other therapeutic agent.
  • THIAZOLE COMPOUNDS AND METHODS OF USE
    申请人:Zhang Suoming
    公开号:US20120108576A1
    公开(公告)日:2012-05-03
    The present invention provides compounds, salts and hydrates of Formula I, wherein the variables Ar 1 , R 2 , R 3 , R 4 , r, q, and t are defined herein. Certain compounds of Formula I described herein possess potent antiviral activity. The invention also provides compounds of Formula I that are potent and/or selective inhibitors of Hepatitis C virus replication. Certain compounds described herein inhibit assembly of the HCV replication complex. The invention also provides pharmaceutical compositions containing one or more compounds of Formula I, or a salt, solvate, or acylated prodrug of such compounds, and one or more pharmaceutically acceptable carriers, excipients, or diluents. The invention further comprises methods of treating patients suffering from certain infectious diseases by administering to such patients an amount of a compound of Formula I effective to reduce signs or symptoms of the disease. These infectious diseases include viral infections, particularly HCV infections. The invention is particularly includes methods of treating human patients suffering from an infectious disease, but also encompasses methods of treating other animals, including livestock and domesticated companion animals, suffering from an infectious disease. Methods of treatment include administering a compound of Formula I as a single active agent or administering a compound of Formula I in combination with on or more other therapeutic agent.
  • US8088806B2
    申请人:——
    公开号:US8088806B2
    公开(公告)日:2012-01-03
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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 (E)-butyl 3-(6-methylthiazolo[3,2-b][1,2,4]triazol-5-yl)acrylate (E)-6-methyl-5-styrylthiazolo[3,2-b][1,2,4]triazole Dimethyl-carbamic acid 6-methyl-thiazolo[3,2-b][1,2,4]triazol-2-yl ester 1-(6-methyl-2-(thiophen-2-yl)thiazolo[3,2-b][1,2,4]triazol-5-yl)ethan-1-one (+/-)-1-[6-methyl-2-(2-thienyl)[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl]ethanol 6-(4-methoxyphenyl)-5-pyrimidin-5-yl-thiazolo[3,2-b][1,2,4]triazole 6-methyl-5-(pyrimidin-5-yl)thiazolo[3,2-b][1,2,4]triazole 6-(p-tolyl)-5-pyrimidin-5-yl-thiazolo[3,2-b][1,2,4]triazole (+/-)-1-(3-bromo-5-methyl[1,3]thiazolo[2,3-c][1,2,4]triazol-6-yl)ethanol 3-acethoxymethyl-7-acetyl-6-methyl-5-(2-methyl-4-thiazolyl)pyrrolo<2,1-b>thiazole 1-(6-methylthiazolo[3,2-b][1,2,4]triazol-5-yl)-ethan-1-one oxime 6-methyl-5-(pyridin-4-yl)thiazolo[3,2-b][1,2,4]triazole 1-(5-Phenyl-thiazolo[2,3-c][1,2,4]triazol-3-yl)-ethanone; hydrochloride (E)-N-tert-butyl-3-(6-methylthiazolo[3,2-b][1,2,4]triazol-5-yl)acrylamide (+/-)-1-(5-methyl[1,3]thiazolo[2,3-c][1,2,4]triazol-6-yl)ethanol 2-Ethyl-5-p-chlorophenylthiazolo<3,2-b>-s-triazole 4-Imino-6-phenyl-4H-thiazolo[2,3-c][1,2,4]triazine-3-carbonitrile Isopropyl-phosphoramidic acid ethyl ester 6-methyl-thiazolo[3,2-b][1,2,4]triazol-2-yl ester 2-Ethyl-5-phenylthiazolo<3,2-b>-s-triazole 2-(6-methyl[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)-2-propanol Dimethyl-phosphinothioic acid O-(6-methyl-thiazolo[3,2-b][1,2,4]triazol-2-yl) ester 2-Hydroxy-6-methyl-thiazolo[3,2-b][1,2,4]triazole-5-carboxylic acid ethyl ester 6-(2-Furanylmethylene)-3-methylthiazolo[2,3-c]-1,2,4-triazol-5(6H)-one 3-Methyl-6-methoxy-1,2,4-triazolo-(2,3-b)-thiazol Thiazolo[2,3-c]-1,2,4-triazole-3-methanamine, 5-(3-fluoro-4-methoxyphenyl)-I+/--methyl- 2-[(4-methoxyphenyl)methyl]-6-methylthiazolo[3,2-b]-1,2,4-triazole-5-carboxylic acid ethyl ester 2-[(4-methoxyphenyl)ethyl]thiazolo[3,2-b]-1,2,4-triazole-6-acetic acid ethyl ester Thiophosphoric acid O-(5-bromo-6-ethyl-thiazolo[3,2-b][1,2,4]triazol-2-yl) ester O',O''-diethyl ester 3-(1-(5,7-diisopropyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl)-5-(4-methyl-cyclohexyl)-1,2,3,6-tetrahydro-pyridin-4-yl)-5-phenyl-thiophene-2-carboxylic acid (E)-6-(4-N,N-dimethylaminobenzylidene)-2-benzylthiazolo[3,2-b][1,2,4]triazol-5(6H)-one 2-[(4-methoxyphenyl)methyl]thiazolo[3,2-b]-1,2,4-triazole-6-acetic acid ethyl ester 5-D-6-phenylthiazolo[3,2-b][1,2,4]triazole 2-[(4-methoxyphenyl)ethyl]-6-methylthiazolo[3,2-b]-1,2,4-triazole-5-carboxylic acid ethyl ester 5,6-diphenylthiazolo[3,2-b]-1,2,4-triazole 1-(4-fluorobenzyl)-4-(4-methyl-5-(5-methyl-1H-1,2,4-triazol-3-yl)thiazol-2-yl)-1H-1,2,4-triazol-5(4H)-one (E)-6-methyl-5-(4-methylstyryl)thiazolo[3,2-b][1,2,4]triazole ethyl 1-(2-fluorobenzyl)-3-(thiazol-2-yl)-1H-1,2,4-triazole-5-carboxylate 6-benzoylamino-2-benzyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazolium betaine 2-(1-ethyl-1H-pyrazol-4-yl)-5-iodo-imidazo[2,1-b][1,3,4]thiadiazole 2-Hydroxy-6-methyl-thiazolo[3,2-b][1,2,4]triazole-5-carboxylic acid methyl ester