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2-(2-Chlorophenyl)-8-fluoro-4-thiophen-2-yl-2,5-dihydro-1,5-benzothiazepine | 1160496-29-6

中文名称
——
中文别名
——
英文名称
2-(2-Chlorophenyl)-8-fluoro-4-thiophen-2-yl-2,5-dihydro-1,5-benzothiazepine
英文别名
——
2-(2-Chlorophenyl)-8-fluoro-4-thiophen-2-yl-2,5-dihydro-1,5-benzothiazepine化学式
CAS
1160496-29-6
化学式
C19H13ClFNS2
mdl
——
分子量
373.902
InChiKey
JFYHGCNFWJTJKE-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):
    6.2
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    65.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-(2-chlorophenyl)-1-(2-thienyl)-2-propenone2-氨基-5-氟苯硫酚盐酸 作用下, 以 乙醇 为溶剂, 以60%的产率得到2-(2-Chlorophenyl)-8-fluoro-4-thiophen-2-yl-2,5-dihydro-1,5-benzothiazepine
    参考文献:
    名称:
    Syntheses of 1,5-Benzothiazepines: Part XXXVI—Syntheses and Antimicrobial Evaluation of 2-(2-Chlorophenyl)-4-(4-chlorophenyl/2-thienyl)-2,5-dihydro-8-substituted-1,5-benzothiazepines
    摘要:
    Six 5-substituted-2-aminobenzenethiols have been reacted with 3-(2-chlorophenyl)-1-(4-chlorophenyl)-2-propenone and 3-(2-chlorophenyl)-1-(2-thienyl)-2-propenone in dry ethanol saturated with dry HCl gas, to obtain twelve new compounds, 8-substituted-2-(2-chlorophenyl)-4-(4-chlorophenyl/2-thienyl)-2,5-dihydro-1,5-benzothiazepines in satisfactory yields. The structures of the final products have been assigned by elemental microanalyses data for elements, C, H, and N and by IR, 1H NMR, and mass spectroscopies. The synthesized compounds have been evaluated for their relative antimicrobial activity against the gram-positive bacteria, Staphylococcus aureus, gram-negative bacteria, Pseudomonas aeruginosa and the fungus, Candida albicans. The compounds have been found to show little antibacterial activity, but interestingly, showed significant antifungal activity.
    DOI:
    10.1080/10426500802048920
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文献信息

  • Syntheses of 1,5-Benzothiazepines: Part XXXVI—Syntheses and Antimicrobial Evaluation of 2-(2-Chlorophenyl)-4-(4-chlorophenyl/2-thienyl)-2,5-dihydro-8-substituted-1,5-benzothiazepines
    作者:Seema Pant、Priyanka Sharma、Umesh C. Pant
    DOI:10.1080/10426500802048920
    日期:2008.11.7
    Six 5-substituted-2-aminobenzenethiols have been reacted with 3-(2-chlorophenyl)-1-(4-chlorophenyl)-2-propenone and 3-(2-chlorophenyl)-1-(2-thienyl)-2-propenone in dry ethanol saturated with dry HCl gas, to obtain twelve new compounds, 8-substituted-2-(2-chlorophenyl)-4-(4-chlorophenyl/2-thienyl)-2,5-dihydro-1,5-benzothiazepines in satisfactory yields. The structures of the final products have been assigned by elemental microanalyses data for elements, C, H, and N and by IR, 1H NMR, and mass spectroscopies. The synthesized compounds have been evaluated for their relative antimicrobial activity against the gram-positive bacteria, Staphylococcus aureus, gram-negative bacteria, Pseudomonas aeruginosa and the fungus, Candida albicans. The compounds have been found to show little antibacterial activity, but interestingly, showed significant antifungal activity.
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同类化合物

齐瑞索韦 马来酸地尔硫卓 贝匹斯汀 苯甲醇,-α--(1-氨基-2-丙烯基)-(9CI) 硫西新 盐酸地尔硫卓O-去乙酰化物 盐酸地尔硫卓 盐酸地尔硫卓 氯噻平 氟水杨基<邻羟苄基>醛 尼克噻嗪 富马酸喹硫平 奎硫平去羟乙基杂质 奎硫平乙醚(富马酸) 奎硫平DBTO砜 地尔硫卓肾上腺素 地尔硫卓杂质8 地尔硫卓杂质5 地尔硫卓杂质4 地尔硫卓杂质 地尔硫卓EP杂质A 地尔硫卓-d6 地尔硫卓 喹硫平砜 喹硫平杂质E 喹硫平杂质DHCl 喹硫平亚砜 喹硫平二聚体 喹硫平EP杂质S盐 喹硫平 N-氧化物 喹硫平 哌苯硫氮杂卓 哌嗪,3,3-二甲基-1-(1-甲基乙基)-(9CI) 去乙酰基地尔硫卓N-氧化物 去乙酰地尔硫卓 去乙酰-O-去甲基地尔硫卓 克仑硫卓 倍氯米松杂质D 二苯并[b,f]咪唑并[1,2-d][1,4]硫氮杂卓 二苯并[b,f][1,4]硫氮杂卓-11-胺 二苯并[b,f][1,4]硫氮杂卓-11-[10H]酮 二苯并(b,f)-1,2,4-三唑并(4,3-d)(1,4)硫氮杂卓-6-胺 [5-(2-二甲基氨基乙基)-8-甲基-2-(4-甲基苯基)-4-氧代-2,3-二氢-1,5-苯并硫氮杂卓-3-基]乙酸酯 [5-(2-二甲基氨基乙基)-2-(4-甲氧基苯基)-4-氧代-2,3-二氢-1,5-苯并硫氮杂卓-3-基]乙酸酯 [2H6]-乙酰基地尔硫卓 [1,3]噻唑并[4,5-I][1,5]苯并硫氮杂卓 [(2S,3S)-3-乙酰氧基-2-(4-乙氧基苯基)-4-氧代-2,3-二氢-1,5-苯并硫氮杂卓-5-基]-乙基-二甲基铵碘化物 [(2S,3S)-2-(4-甲氧基苯基)-5-[2-(甲基-丙-2-基氨基)乙基]-4-氧代-2,3-二氢-1,5-苯并硫氮杂卓-3-基]乙酸酯 N-去甲地尔硫卓马来酸盐 N,N-二去甲基地尔硫卓盐酸盐