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1,2,3-Triazolo<5,1-b>thiazole | 54101-88-1

中文名称
——
中文别名
——
英文名称
1,2,3-Triazolo<5,1-b>thiazole
英文别名
Thiazolo[3,2-c][1,2,3]triazole;[1,3]thiazolo[3,2-c]triazole
1,2,3-Triazolo<5,1-b>thiazole化学式
CAS
54101-88-1
化学式
C4H3N3S
mdl
——
分子量
125.154
InChiKey
YXNXWFFPNAIBPN-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):
    0.5
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    58.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1,2,3-Triazolo<5,1-b>thiazole 在 selenium(IV) oxide 作用下, 以 1,4-二氧六环 为溶剂, 以79%的产率得到2-醛基噻唑
    参考文献:
    名称:
    1,2,3-triazolo[5,1-b]thiazoles; synthesis and properties
    摘要:
    The synthesis of 1,2,3-triazolo[5,1-b]thiazole (15) and its 3-methyl- (16) and 3-phenyl- (17) derivatives is reported, together with their spectra, quaternisation, and ring opening reactions.
    DOI:
    10.1016/s0040-4020(01)87090-3
  • 作为产物:
    描述:
    4-methyl-N-(1,3-thiazol-2-ylmethylideneamino)benzenesulfonamidesodium hydroxide四丁基溴化铵 作用下, 以 二氯甲烷 为溶剂, 反应 72.0h, 以49%的产率得到1,2,3-Triazolo<5,1-b>thiazole
    参考文献:
    名称:
    L'abbe, Gerrit; Luyten, Ingrid; Frederix, Ann, Bulletin des Societes Chimiques Belges, 1990, vol. 99, # 6, p. 389 - 390
    摘要:
    DOI:
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文献信息

  • 1,2,3-Triazolo[5,1-b]thiazoles. Part 2 Lithiation experiments leading to 2,4-disubstituted thiazoles
    作者:Gurnos Jones、Hermione Ollivierre、L.S. Fuller、J.H. Young
    DOI:10.1016/s0040-4020(01)87091-5
    日期:1991.1
    3-Methyltriazolothiazole (2) and 3-phenyltriazolothiazole (3) were regiospecifically lithiated at position 6, triazolothiazole (1) at position 6 and 3 with the former predominating. The lithiated triazolothiazoles (4), (10) and (11) reacted with a number of electrophiles to give x:6-disubstituted triazolothiazoles, which could be converted into 2,4-disubstituted thiazoles.
  • L'abbe, Gerrit; Luyten, Ingrid; Frederix, Ann, Bulletin des Societes Chimiques Belges, 1990, vol. 99, # 6, p. 389 - 390
    作者:L'abbe, Gerrit、Luyten, Ingrid、Frederix, Ann、Gelinne, Marleen
    DOI:——
    日期:——
  • 1,2,3-triazolo[5,1-b]thiazoles; synthesis and properties
    作者:Gurnos Jones、Hermione Ollivierre、L.S. Fuller、J.H. Young
    DOI:10.1016/s0040-4020(01)87090-3
    日期:1991.1
    The synthesis of 1,2,3-triazolo[5,1-b]thiazole (15) and its 3-methyl- (16) and 3-phenyl- (17) derivatives is reported, together with their spectra, quaternisation, and ring opening reactions.
  • L'abbe, Gerrit; Luyten, Ingrid; Toppet, Suzanne, Journal of Heterocyclic Chemistry, 1992, vol. 29, # 4, p. 713 - 717
    作者:L'abbe, Gerrit、Luyten, Ingrid、Toppet, Suzanne
    DOI:——
    日期:——
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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 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