摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

methyl 2-[3-(3-butenyl)-4-oxo-2-thioxo-1,3-thiazolidin-5-yliden]acetate | 1140921-03-4

中文名称
——
中文别名
——
英文名称
methyl 2-[3-(3-butenyl)-4-oxo-2-thioxo-1,3-thiazolidin-5-yliden]acetate
英文别名
——
methyl 2-[3-(3-butenyl)-4-oxo-2-thioxo-1,3-thiazolidin-5-yliden]acetate化学式
CAS
1140921-03-4
化学式
C9H9NO3S2
mdl
——
分子量
243.307
InChiKey
DNMMXIUIAOGJPH-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

物化性质

  • 熔点:
    140-142 °C
  • 沸点:
    332.0±52.0 °C(Predicted)
  • 密度:
    1.40±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.09
  • 重原子数:
    15.0
  • 可旋转键数:
    3.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    46.61
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    methyl 2-[3-(3-butenyl)-4-oxo-2-thioxo-1,3-thiazolidin-5-yliden]acetate 、 在 三乙胺 作用下, 以 乙醇 为溶剂, 反应 0.33h, 以77%的产率得到2-allyl-4-amino-1,3,10-trioxo-1,2,3,10-tetrahydroindeno[2,1-e]-isoindole-5-carbonitrile
    参考文献:
    名称:
    取代邻苯二甲酰亚胺的合成通过超声促进一锅多组分反应
    摘要:
    在这项工作中,描述了一种直接合成取代的邻苯二甲酰亚胺的新策略,其中包括碱介导的迈克尔加成/分子内环化/ [1,5] -H移位/ CS 2裂解/芳香化/ 2的亲核酰基取代反应-(4-氧代-2-硫代噻吩并恶唑烷-5-亚烷基)乙酸酯和α,α-二氰基烯烃在超声(US)辐射下。该方法的一些优点如下:操作简单,原料易得,化学选择性级联工艺,合成有用的收率以及通过利用US辐射作为能源并使用乙醇作为溶剂的绿色条件。
    DOI:
    10.1021/acs.joc.0c02245
  • 作为产物:
    参考文献:
    名称:
    Application of the β-cyclodextrin supramolecules as a green accelerator hosts in one-step preparation of highly functionalised rhodanine scaffolds
    摘要:
    beta-Cyclodextrin (beta-CD) supramolecule was found to be a convenient, green and economical tool in one-pot synthesis of rhodanine scaffolds as a highly efficient mediating agent in aqueous media in which the reaction accelerated to complete in 15min and room temperature. In this work, amines reacted with equimolar ratio of CS2 (not excess ratio of CS2) and then with activated acetylenes in the presence of beta-CD in aqueous media.
    DOI:
    10.1080/10610278.2014.890200
点击查看最新优质反应信息

文献信息

  • EtOAc-dispersed magnetic nanoparticles (DMNPs) of γ-Fe2O3 in the single-pot domino preparation of 5-oxo-2-thioxo-3-thiophenecarboxylate derivatives
    作者:Sadegh Rostamnia
    DOI:10.1016/j.crci.2013.03.002
    日期:2013.11
    Résumé EtOAc-dispersed magnetic nanoparticles (DMNPs) of γ-Fe2O3 represent a straightforward and green catalyst for the rapid three-component synthesis of 5-oxo-2-thioxo-3-thiophenecarboxylate derivatives as rhodanine skeletons via a single-pot domino process. The rhodanines were prepared over magnetic nanoparticles of γ-Fe2O3 without any salt or additives. Dispersed nano-γ-Fe2O3 have many advantages, such as stability in air, reusability, reactions with high efficiency, simple separation with magnetic external field from mixture reactions, chemical stability, and also low toxicity.
    摘要 EtOAc-分散的γ-Fe2O3磁性纳米粒子(DMNPs)是一种直接、绿色的催化剂,可通过单锅多米诺过程,以罗丹宁为骨架,快速合成 5-氧代-2-酮-3-噻吩羧酸酯衍生物的三组分化合物。这些罗丹宁是在γ- 的磁性纳米粒子上制备的,不含任何盐或添加剂。分散纳米γ- 具有许多优点,如在空气中稳定、可重复使用、反应效率高、利用磁场从混合物反应中分离简单、化学性质稳定以及毒性低等。
  • A simple and effective approach to the synthesis of rhodanine derivatives via three-component reactions in water
    作者:Abdolali Alizadeh、Sadegh Rostamnia、Nasrin Zohreh、Reza Hosseinpour
    DOI:10.1016/j.tetlet.2008.12.107
    日期:2009.4
    A facile and direct synthetic entry to rhodanine derivatives via the three-component coupling of carbon disulfide, primary amines, and acetylenic esters under neutral conditions in water is reported.
    据报道,在中性条件下,通过二硫化碳伯胺和炔属酯的三组分偶联,可以很容易地直接合成罗丹宁生物
  • A Rapid, Catalyst-Free, Three-Component Synthesis of Rhodanines in Water Using Ultrasound
    作者:Sadegh Rostamnia、Kamran Lamei
    DOI:10.1055/s-0030-1260158
    日期:2011.10
    A green, efficient, rapid, high-yielding, catalyst-free method for the synthesis of rhodanines in water using ultrasonic irradiation is described. The procedure is straightforward and the rhodanine products are isolated by simple filtration.
    本文描述了一种绿色、高效、快速、高产、无催化剂的超声波辐射法,用于在中合成罗丹宁。该方法操作简单,罗丹宁产品可通过简单过滤进行分离。
  • The use of κ-carrageenan/Fe3O4 nanocomposite as a nanomagnetic catalyst for clean synthesis of rhodanines
    作者:Sadegh Rostamnia、Behzad Zeynizadeh、Esmail Doustkhah、Ali Baghban、Khadijeh Ojaghi Aghbash
    DOI:10.1016/j.catcom.2015.05.002
    日期:2015.8
    In this work, magnetically separable Fe3O4 nanoparticles were synthesized in the presence of natural K-carrageenan (KCAR) biopolymer to provide Fe3O4@KCAR. FT-IR analysis, scanning electron microscopy (SEM), X-ray diffraction, VSM analysis, and SEM-EDAX were incorporated for the characterization of Fe3O4@KCAR nanocomposite. And then, the first catalytic report of Fe3O4@KCAR with no post-modification was achieved by studying its catalytic activity in the multicomponent reaction of rhodanine synthesis. Based on this study, Fe3O4@KCAR was an efficient, magnetically separable and recyclable, water-dispersible and green catalyst with natural source. This catalyst also showed 9-run recyclability with no significant yield decrease. (C) 2015 Elsevier B.V. All rights reserved.
  • Cetyltrimethylammonium bromide-surfactant aqueous micelles as a green and ultra-rapid reactor for synthesis of 5-oxo-2-thioxo-2,5-dihydro-3-thiophenecarboxylate derivatives
    作者:Sadegh Rostamnia、Ziba Karimi、Mehdi Ghavidel
    DOI:10.1080/17415993.2012.662980
    日期:2012.6
    Aqueous cetyltrimethylammonium bromide-surfactant micelles were found to be an efficient and rapid reactor system for the synthesis of rhodanine by a three-component reaction of amine, carbon disulfide, and activated acetylene. The advantages of this method are the use of a water medium and a simple and easy workup resulting in a green and direct synthetic method to give excellent yields of rhodanine derivatives.
查看更多

同类化合物

(R)-4-异丙基-2-恶唑烷硫酮 麻黄恶碱 顺-八氢-2H-苯并咪唑-2-酮 顺-1-(4-氟苯基)-4-[1-(4-氟苯基)-4-羰基-1,3,8-三氮杂螺[4.5]癸-8-基]环己甲腈 非达司他 降冰片烯缩醛3-((1S,2S,4S)-双环[2.2.1]庚-5-烯-2-羰基)恶唑烷-2-酮 阿齐利特 阿那昔酮 阿洛双酮 阿帕鲁胺 阿帕他胺杂质2 铟烷-2-YL-甲基胺盐酸 钾3-{2-[3-氰基-3-(十二烷基磺酰基)-2-丙烯-1-亚基]-1,3-噻唑烷-3-基}-1-丙烷磺酸酯 钠2-{[4,5-二羟基-3-(羟基甲基)-2-氧代-1-咪唑烷基]甲氧基}乙烷磺酸酯 重氮烷基脲 詹氏催化剂 解草恶唑 解草噁唑 表告依春 螺莫司汀 螺立林 螺海因氮丙啶 螺[咪唑烷-4,3'-吲哚啉]-2,2',5-三酮 螺[1-氮杂双环[2.2.2]辛烷-8,5'-咪唑烷]-2',4'-二酮 苯甲酸,4-氟-,2-[5,7-二(三氟甲基)-1,8-二氮杂萘-2-基]-2-甲基酰肼 苯氰二硫酸,1-氰基-1-甲基-4-氧代-4-(2-硫代-3-噻唑烷基)丁酯 苯妥英钠杂质8 苯妥英钠 苯妥英-D10 苯妥英 苯基硫代海因半胱氨酸钠盐 苯基硫代乙内酰脲-谷氨酸 苯基硫代乙内酰脲-蛋氨酸 苯基硫代乙内酰脲-苯丙氨酸 苯基硫代乙内酰脲-色氨酸 苯基硫代乙内酰脲-脯氨酸 苯基硫代乙内酰脲-缬氨酸 苯基硫代乙内酰脲-异亮氨酸 苯基硫代乙内酰脲-天冬氨酸 苯基硫代乙内酰脲-亮氨酸 苯基硫代乙内酰脲-丙氨酸 苯基硫代乙内酰脲-D-苏氨酸 苯基硫代乙内酰脲-(NΕ-苯基硫代氨基甲酰)-赖氨酸 苯基乙内酰脲-甘氨酸 苏氨酸-1-(苯基硫基)-2,4-咪唑烷二酮(1:1) 色氨酸标准品002 膦酸,(2-羰基-1-咪唑烷基)-,二(1-甲基乙基)酯 脱氢-1,3-二甲基尿囊素 脱氢-1,3,8-三甲基尿囊素 聚(d(A-T)铯)