2-((3,4,4-trifluorobut-3-en-1-yl)thio)benzothiazole | 27443-04-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻唑类
• 英文名称: 2-((3,4,4-trifluorobut-3-en-1-yl)thio)benzothiazole
• 英文别名: 2-(3,4,4-Trifluor-3-butenylthio)-benzthiazol；2-(3,4,4-trifluoro-but-3-enylsulfanyl)-benzothiazole；2-[(3,4,4-Trifluoro-3-butenyl)sulfanyl]-1,3-benzothiazole；2-(3,4,4-trifluorobut-3-enylsulfanyl)-1,3-benzothiazole
• CAS: 27443-04-5
• 化学式: C₁₁H₈F₃NS₂
• 分子量: 275.318
• InChiKey: UESPPBXGEOHJOM-UHFFFAOYSA-N

物化性质

• 沸点：
  351.5±52.0 °C(Predicted)
• 密度：
  1.41±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  17
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  66.4
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2-((3,4,4-trifluorobut-3-en-1-yl)thio)benzothiazole 在 双氧水 、 溶剂黄146 作用下， 以 水 为溶剂， 以63.9%的产率得到2-((3,4,4-trifluorobut-3-en-1-yl)sulfonyl)benzothiazole
  参考文献：
  名称：

  Fluoroalkane thioheterocyclic derivatives and their antitumor activity

  摘要：

  Two series of novel trifluorobutenyl derivatives of heterocyclic with convenient and efficient synthesis methods and their antitumor activity on three cell lines have been reported for the first time. The derivatives were synthesized by the nucleophilic substitution between 4-bromo-1,1,2-trifluorobutene-1-ene and commercially available nitrogen-containing heterocycles with sulfydryl or monosubstituted malononitrile. The twenty-four new compounds were characterized by (HNMR)-H-1, (CNMR)-C-13 and HR-MS. Totally, thirty-seven compounds were evaluated for the antitumor activity on three cancer cell lines (SH-SY5Y, MCF-7 and HepG2) using conventional MIT assay. The pharmacological results indicated that the compounds 3c, 3h, 4c, 8, 9, 10 and 11 showed potent to moderate antitumor activity against three cancer cell lines, with IC50 values ranging between 0.4 mu M and 41.5 mu M. Even though they had less active than the reference compound taxol against MCF-7 and HepG2 lines, but they were better than the reference compound noscapine against SH-SY5Y cells, especially the compound 3h with a IC50 value of 0.4 mu M. (C) 2015 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2015.02.031
• 作为产物：
  描述：

  4-溴-1,1,2-三氟-1-丁烯 、 2-巯基苯并噻唑 在 potassium carbonate 作用下， 以 乙腈 为溶剂， 以76.9%的产率得到2-((3,4,4-trifluorobut-3-en-1-yl)thio)benzothiazole
  参考文献：
  名称：

  Fluoroalkane thioheterocyclic derivatives and their antitumor activity

  摘要：

  Two series of novel trifluorobutenyl derivatives of heterocyclic with convenient and efficient synthesis methods and their antitumor activity on three cell lines have been reported for the first time. The derivatives were synthesized by the nucleophilic substitution between 4-bromo-1,1,2-trifluorobutene-1-ene and commercially available nitrogen-containing heterocycles with sulfydryl or monosubstituted malononitrile. The twenty-four new compounds were characterized by (HNMR)-H-1, (CNMR)-C-13 and HR-MS. Totally, thirty-seven compounds were evaluated for the antitumor activity on three cancer cell lines (SH-SY5Y, MCF-7 and HepG2) using conventional MIT assay. The pharmacological results indicated that the compounds 3c, 3h, 4c, 8, 9, 10 and 11 showed potent to moderate antitumor activity against three cancer cell lines, with IC50 values ranging between 0.4 mu M and 41.5 mu M. Even though they had less active than the reference compound taxol against MCF-7 and HepG2 lines, but they were better than the reference compound noscapine against SH-SY5Y cells, especially the compound 3h with a IC50 value of 0.4 mu M. (C) 2015 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2015.02.031

文献信息

• BENZOXAZOLE AND BEZOTHIAZOLE DERIVATIVES
  申请人：ZENECA LIMITED

  公开号：EP0660830A1

  公开（公告）日：1995-07-05
• US5451594A
  申请人：——

  公开号：US5451594A

  公开（公告）日：1995-09-19
• [EN] BENZOXAZOLE AND BEZOTHIAZOLE DERIVATIVES<br/>[FR] DERIVES DE BENZOXAZOLE ET DE BENZOTHIAZOLE
  申请人：ZENECA LIMITED

  公开号：WO1994006782A1

  公开（公告）日：1994-03-31

  (EN) The invention provides novel compounds of formula (I) having nematicidal, insecticidal, acaricidal and fungicidal properties, compositions comprising them and processes and intermediates for their preparation, wherein X is oxygen or sulphur; n is 0, 1 or 2; R1, R2, R3, and R4 are independently selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, alkylcycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted aryloxy, optionally substituted arylalkoxy, alkoxy, alkenyloxy, alkynyloxy, hydroxyalkyl, alkoxyalkyl, alkylthio, alkenylthio, alkynylthio, haloalkyl, haloalkenyl, haloalkynyl, haloalkoxy, haloalkenyloxy, haloalkynyloxy, haloalkylthio, haloalkenylthio, haloalkynylthio, halogen, hydroxy, cyano, nitro, -NR5R6, -NR7COR8, -NR9SO2R10, -N(SO2-R11)(SO2-R12), -COR13, -CONR14R15, -COOR16, -OCOR17, -OSO2R18, -SO2NR19R20, -SO2R21, -SOR22, -CSNR23R24, -SiR25R26R27, -OCH2CO2R28, -OCH2CH2CO2R29, -CONR30SO2R31 and -SO2Z; or an adjacent pair of R1, R2, R3 and R4 when taken together form a fused 5- or 6-membered carbocyclic or heterocyclic ring; R5, R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18, R19, R20, R21, R22, R23, R24, R25, R26, R27, R28, R29, R30 and R31 are independently selected from hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl, optionally substituted aryl and optionally substituted aryalkyl; and Z is halogen.(FR) L'invention concerne des nouveaux composés de formule (I) ayant des propriétés nématicides, insecticides, acaricides et fongicides, des compositions comprenant ces composés et des procédés ainsi que des intermédiaires pour leur préparation, dans laquelle X représente oxygène ou soufre; N est égal à 0, 1 ou 2; R1, R2, R3 et R4 sont sélectionnés indépendamment parmi hydrogène, alkyle, alkényle, alkynyle, cycloalkyle, alkylcycloalkyle, aryle éventuellement substitué, arylalkyle éventuellement substitué, aryloxy éventuellement substitué, arylalkyloxy éventuellement substitué, alcoxy, alkoxy, alkenyloxy, alkynyloxy, hydroxyalkyle, alkoxyalkyle, alkylthio, alkénylthio, alkynylthio, haloalkyle, haloalkényle, haloalkynyle, haloalkoxy, haloalkenyloxy, haloalkynyloxy, haloalkylthio, haloalkénylthio, haloalkynylthio, halogène, hydroxy, cyano, nitro, -NR5R6, -NR7COR8, -NR9SO2R10, -N(SO2-R11)(SO2-R12), -COR13, -CONR14R15, -COOR16, -OCOR17, -OSO2R18, -SO2NR19R20, -SO2R21, -SOR22, -CSNR23R24, -SiR25R26R27, -OCH2CO2R28, -OCH2CH2CO2R29, -CONR30SO2R31 et -SO2Z, ou une paire adjacente refroupant R1, R2, R3 et R4 lorsqu'ils sont pris ensemble forment un cycle carboxylique ou hétérocyclique fusionné à 5 ou 6 chaînons; R5, R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16, R17, R18, R9, R20, R21, R22, R23, R24, R25, R26, R27, R28, R29, R30 et R31 sont sélectionnés indépendamment parmi hydrogène, alkyle, alkényle, alkynyle, haloalkyle, haloalkényle, haloalkynyle, aryle éventuellement substitué et arylalkyle éventuellement substitué; et Z représente halogène.