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1H-3-(4'-thiazolyl)indole | 22258-53-3

中文名称
——
中文别名
——
英文名称
1H-3-(4'-thiazolyl)indole
英文别名
4-(Indol-3-yl)thiazole;4-(1H-indol-3-yl)-1,3-thiazole
1H-3-(4'-thiazolyl)indole化学式
CAS
22258-53-3
化学式
C11H8N2S
mdl
——
分子量
200.264
InChiKey
WMACHIODVOSLNK-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):
    2.7
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    56.9
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    3-碘吲哚4-二甲氨基吡啶四(三苯基膦)钯 、 sodium carbonate 、 三乙胺三苯基膦 作用下, 以 1,4-二氧六环二氯甲烷 为溶剂, 反应 23.5h, 生成 1H-3-(4'-thiazolyl)indole
    参考文献:
    名称:
    通过 Masuda Borylation-Suzuki Arylation (MBSA) 序列一锅法合成 Camalexins 和 3,3'-联吲哚
    摘要:
    从 N 保护的 3-碘吲哚开始的 Masuda 硼酸化/铃木芳基化 (MBSA) 序列已成功扩展到芳基化步骤中五元杂环和吲哚的偶联,这是以前开发的 MBSA 方法无法实现的。通过这种方法,该方法的一锅法特性以及简单催化剂体系的使用得到了保留。该方法的适用性已通过 camalexins 和 3,3'-联吲哚的轻松合成得到证明,这些化合物由于其显着的抗真菌、抗菌和细胞毒性活性而受到特别关注。
    DOI:
    10.1002/ejoc.201300133
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文献信息

  • [EN] HETEROARYL COMPOUNDS AS AGROCHEMICAL FUNGICIDES<br/>[FR] COMPOSÉS HÉTÉROARYLES EN TANT QUE FONGICIDES AGROCHIMIQUES
    申请人:BASF SE
    公开号:WO2018210659A1
    公开(公告)日:2018-11-22
    Heteroaryl compounds as agrochemical fungicides Formula (I) The present invention relates to heteroaryl compounds of formula (I) or a compound in the form of a stereoisomer, an agriculturally acceptable salt, a tautomer, an isotopic form, a N-oxide, a S- oxide, a prodrug or mixture thereof. The present invention further relates to the use of a com- pound of formula (I). Furthermore, the present invention relates to methods for combating phy- topathogenic harmful fungi, which methods comprising the steps of treatment of the phytopatho- genic fungi, the plant orthe plant propagation material selected from seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants, including seedlings and young plants to be protected against fungal attack, stored materials or harvest, or alternatelythe locus or soil or soil substituents or surfaces therefrom, with at least one compound of formula (I).
    杂环烷基化合物作为农用杀菌剂的化学式(I)。本发明涉及化学式(I)的杂环烷基化合物或立体异构体形式的化合物、农业可接受的盐、互变异构体、同位素形式、N-氧化物、S-氧化物、前药或其混合物。本发明还涉及化学式(I)化合物的使用。此外,本发明涉及用于对抗植物病原有害真菌的方法,包括处理植物病原真菌、植物或植物繁殖材料(包括种子、根、水果、块茎、球茎、根茎、新芽等植物部分,包括需要受到真菌攻击保护的幼苗和幼苗)、储存物料或收获物料的步骤,或者选择定位或土壤或土壤替代物或其表面,用化学式(I)的至少一种化合物进行处理。
  • Indole derivatives
    作者:Yu. I. Smushkevich、Ts. M. Babueva、N. N. Suvorov
    DOI:10.1007/bf01031770
    日期:——
  • [EN] HETEROARYL COMPOUNDS AS AGROCHEMICAL FUNGICIDES<br/>[FR] COMPOSÉS HÉTÉROARYLE EN TANT QUE FONGICIDES AGROCHIMIQUES
    申请人:BASF SE
    公开号:WO2018210660A1
    公开(公告)日:2018-11-22
    The present invention relates to heteroaryl compounds of formula (I) or a compound in the form of a stereoisomer, an agriculturally acceptable salt, a tautomer, an isotopic form, a N-oxide, a S-oxide, a prodrug or mixture thereof. The present invention further relates to the use of a compound of formula (I). Furthermore, the present invention relates to methods for combating phytopathogenic harmful fungi, which methods comprising the steps of treatment of the phytopathogenic fungi, the plant or the plant propagation material selected from seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants, including seedlings and young plants to be protected against fungal attack, stored materials or harvest, or alternately the locus or soil or soil substituents or surfaces therefrom, with at least one compound of formula (I).
  • [EN] HETEROARYL COMPOUNDS AS AGROCHEMICAL FUNGICIDES<br/>[FR] COMPOSÉS HÉTÉROARYLE FAISANT OFFICE DE FONGICIDES AGROCHIMIQUES
    申请人:BASF SE
    公开号:WO2018210661A1
    公开(公告)日:2018-11-22
    The present invention relates to heteroaryl compounds of formula (I) or a compound in the form of a stereoisomer, an agriculturally acceptable salt, a tautomer, an isotopic form, a N-oxide, a S- oxide, a prodrug or mixture thereof. The present invention further relates to the use of a com- pound of formula (I). Furthermore, the present invention relates to methods for combating phy- topathogenic harmful fungi, which methods comprising the steps of treatment of the phytopatho- genic fungi, the plant or the plant propagation material selected from seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants, including seedlings and young plants to be protected against fungal attack, stored materials or harvest, or alternately the locus orsoil or soil substituents or surfaces therefrom, with at least one compound of formula (I).
  • One-Pot Synthesis of Camalexins and 3,3′-Biindoles by the Masuda Borylation-Suzuki Arylation (MBSA) Sequence
    作者:Boris O. A. Tasch、Dragutin Antovic、Eugen Merkul、Thomas J. J. Müller
    DOI:10.1002/ejoc.201300133
    日期:2013.7
    The Masuda borylation/Suzuki arylation (MBSA) sequence starting from N-protected 3-iodoindoles has successfully been extended to the coupling of five-membered heterocycles and indoles in the arylation step, which could not be achieved with previously developed MBSA methods. By this approach the one-pot nature of the method as well as the use of a simple catalyst system has been retained. The applicability
    从 N 保护的 3-碘吲哚开始的 Masuda 硼酸化/铃木芳基化 (MBSA) 序列已成功扩展到芳基化步骤中五元杂环和吲哚的偶联,这是以前开发的 MBSA 方法无法实现的。通过这种方法,该方法的一锅法特性以及简单催化剂体系的使用得到了保留。该方法的适用性已通过 camalexins 和 3,3'-联吲哚的轻松合成得到证明,这些化合物由于其显着的抗真菌、抗菌和细胞毒性活性而受到特别关注。
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