Chemistry-Switzerland最新文献

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Transformation of Linear Alkenyl N-Alkoxy Carbamates into Cyclic Bromo Carbonates. 线性炔基n -烷氧基氨基甲酸酯转化为环碳酸溴酯。
IF 2.4
Chemistry-Switzerland Pub Date : 2025-06-01 Epub Date: 2025-06-16 DOI: 10.3390/chemistry7030099
Shyam Sathyamoorthi, Steven P Kelley
{"title":"Transformation of Linear Alkenyl <i>N</i>-Alkoxy Carbamates into Cyclic Bromo Carbonates.","authors":"Shyam Sathyamoorthi, Steven P Kelley","doi":"10.3390/chemistry7030099","DOIUrl":"https://doi.org/10.3390/chemistry7030099","url":null,"abstract":"<p><p>We present a protocol for the facile conversion of linear alkenyl <i>N</i>-alkoxy carbamates into cyclic bromo carbonates. The reaction is operationally simple, uses widely available, inexpensive reagents, and requires no rigorous exclusion of air or moisture. A broad range of functional groups is compatible, and the reaction diastereoselectivities range from good to excellent. The reactions are scalable, and the product carbonates can be further transformed.</p>","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"7 3","pages":""},"PeriodicalIF":2.4,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12380031/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144978325","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis of Silver Nanocluster-Loaded FAU Zeolites and the Application in Light Emitting Diode 载银纳米团簇FAU沸石的合成及其在发光二极管中的应用
Chemistry-Switzerland Pub Date : 2025-05-30 DOI: 10.3390/chemistry7030090
Tianlong Zheng, Ruihao Huang, Haoran Zhang, Song Ye, Deping Wang
{"title":"Synthesis of Silver Nanocluster-Loaded FAU Zeolites and the Application in Light Emitting Diode","authors":"Tianlong Zheng, Ruihao Huang, Haoran Zhang, Song Ye, Deping Wang","doi":"10.3390/chemistry7030090","DOIUrl":"https://doi.org/10.3390/chemistry7030090","url":null,"abstract":"Silver nanoclusters that are confined inside zeolites can give off intensive tunable emission across the visible region under UV excitation. In this research, a series of silver nanoclusters loaded with R-FAU/Ag (R = Li, Na, K) zeolites were synthesized and then applied as phosphors for LEDs. The XRD and SEM measurements showed the R-FAU/Ag (R = Li, Na, K) zeolites have high crystallinity and a size distribution of 0.7–1.25 μm. Under excitations of 310–330 nm ultraviolet radiation, Li-FAU/Ag, Na-FAU/Ag, and K-FAU/Ag exhibit monotonically declining emission intensities and red-shifted emissions with peak wavelengths of 520, 527, and 535 nm, respectively. By using silicone-based epoxy resin as the packaging material, a series of LEDs were fabricated by mixing R-FAU/Ag (R = Li, Na, K) phosphors. It is indicated that the Li-FAU/Ag-LED shows the strongest intensity of 94.9 mcd, much higher than that of the LEDs made from Na-FAU/Ag (63.7 mcd) and K-FAU/Ag (74.2 mcd) phosphors. Additionally, the chromaticity coordinate of the Li-FAU/Ag-LED is located at (0.2651, 0.4073) and has a high color temperature of 7873 K. Thermal test data showed that upon heating to 440 K, the intensities of R-FAU/Ag (R = Li, Na, K) LEDs decreased to 81%, 79%, and 75% of their initial intensities measured at 280 K, respectively. This research proposes a method for regulating the luminescent properties of silver nanoclusters in FAU zeolite by modifying the extra-framework cations and demonstrates excellent performance in LED products.","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"7 3","pages":"90-90"},"PeriodicalIF":0.0,"publicationDate":"2025-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2624-8549/7/3/90/pdf?version=1748598880","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147916292","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Metal-Free C(sp3)–S Bond Cleavage of Thioethers to Selectively Access Aryl Aldehydes and Dithioacetals 无金属C(sp3) -S键裂解硫醚选择性接近芳基醛和二硫缩醛
Chemistry-Switzerland Pub Date : 2025-05-29 DOI: 10.3390/chemistry7030089
Dan Yuan, Yong Huang, Long Tang, Ke Yang
{"title":"Metal-Free C(sp3)–S Bond Cleavage of Thioethers to Selectively Access Aryl Aldehydes and Dithioacetals","authors":"Dan Yuan, Yong Huang, Long Tang, Ke Yang","doi":"10.3390/chemistry7030089","DOIUrl":"https://doi.org/10.3390/chemistry7030089","url":null,"abstract":"Metal-free C(sp3)–S bond cleavage of thioethers was achieved using NCS as a critical additive. A wide range of arylmethyl thioethers were successfully transformed into aryl aldehydes with satisfactory yields in chloroform. Meanwhile, employing fluorobenzene as the solvent enables the selective formation of dithioacetals from arylmethyl thioethers, achieving moderate to good yields. Notably, dithioacetals were first prepared through a metal-free C(sp3)–S bond cleavage and subsequent thioacetalization process. Furthermore, these simple and efficient approaches also provide complementary strategies for accessing important aryl aldehydes and dithioacetals.","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"7 3","pages":"89-89"},"PeriodicalIF":0.0,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147907730","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Enabling a Reversible Six-Electron Redox Reaction Based on I−/I+ and Br−/Br0 for Aqueous Zinc-Bromine Batteries 基于I−/I+和Br−/Br0的六电子可逆氧化还原反应在锌-溴水溶液电池中的实现
Chemistry-Switzerland Pub Date : 2025-05-02 DOI: 10.3390/chemistry7030075
Jing Zhang, Xiaoxing Ji, Qingxiu Yu, Xixi Zhang, Chuanlin Li, Na Li, Mengzhen Kong, Dingzheng Li, Wenjie Liu, Chenggang Wang, Xijin Xu
{"title":"Enabling a Reversible Six-Electron Redox Reaction Based on I−/I+ and Br−/Br0 for Aqueous Zinc-Bromine Batteries","authors":"Jing Zhang, Xiaoxing Ji, Qingxiu Yu, Xixi Zhang, Chuanlin Li, Na Li, Mengzhen Kong, Dingzheng Li, Wenjie Liu, Chenggang Wang, Xijin Xu","doi":"10.3390/chemistry7030075","DOIUrl":"https://doi.org/10.3390/chemistry7030075","url":null,"abstract":"Zinc-halogen batteries are usually based on two-electron transfer reactions from X− to X2. However, the halogen is capable of being further oxidized to higher valence states, thereby achieving the higher capacity of zinc- halogen batteries. Here, a six-electron reaction based on I−/I+ and Br−/Br0 is activated successfully by introducing KI into the electrolyte. ZIF-8-derived porous carbon (ZPC), serving as the host of halogen, effectively suppresses polybromide/polyiodide shuttle owing to the chemisorption/physical adsorption. Additionally, the adsorption of I− on the surface of the zinc anode effectively inhibits the growth of dendrites and the formation of by-products. Consequently, zinc-bromine batteries exhibit outstanding electrochemical performance, including a specific capacity of 345 mAh g−1 at 1 A g−1 and an excellent capacity retention of 80% after 3000 cycles at 2 A g−1. This strategy provides a novel way for enhancing the electrochemical performance of zinc-halogen batteries.","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"7 3","pages":"75-75"},"PeriodicalIF":0.0,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2624-8549/7/3/75/pdf?version=1746158936","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147882393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Phloretin–Chitosan Nanoparticles and Tamoxifen: Synergistic Modulation of BRCA Genes and Enhanced Sensitization in Breast Cancer 壳聚糖纳米颗粒和他莫昔芬:BRCA基因的协同调节和乳腺癌的增强敏化
Chemistry-Switzerland Pub Date : 2025-04-22 DOI: 10.3390/chemistry7030068
Abeer A. Ageeli, Sahera F. Mohamed
{"title":"Phloretin–Chitosan Nanoparticles and Tamoxifen: Synergistic Modulation of BRCA Genes and Enhanced Sensitization in Breast Cancer","authors":"Abeer A. Ageeli, Sahera F. Mohamed","doi":"10.3390/chemistry7030068","DOIUrl":"https://doi.org/10.3390/chemistry7030068","url":null,"abstract":"This study aims to evaluate the therapeutic potential of phloretin–chitosan nanoparticles (Ph-ChNPs), alone and in combination with the anticancer drug tamoxifen, in modulating breast cancer markers and improving in vivo treatment outcomes. Ph-ChNPs were prepared by ionic gelation in the presence of Tripolyphosphate (TPP) solution as a crosslinker agent. The nanoparticles were characterized using DLS, TEM, UV-VIS and FT-IR spectroscopy. In vitro cytotoxic assay of Ph-ChNPs on MCF-7 breast cancer cell lines revealed anticancer activity with an IC50 value of 32.12 ± 1.63 µg/mL. In vivo studies were carried out on mice, treated with DMBA to induce breast cancer and followed the effect of the prepared nanoparticle, either alone or with combination with tamoxifen, on mice health. The biochemical parameters measured after treatment with Ph-ChNPs alone showed an improvement in lipid profile with decreased total cholesterol (TC) and Triglyceride (TG) levels and increased HDL-c levels. Ph-ChNPs significantly reduced IL-6 and cyclin D1 levels, with a slight increase in cyclin E2 levels. Antioxidant enzyme levels were improved, and oxidative stress markers were reduced. The combination treatment showed a synergistic effect in reducing inflammation and cell proliferation. DMBA-injected mice had substantially increased BRCA1 and BRCA2 gene expression. Ph-ChNP-treated mice showed well-organized mammary gland structures, while DMBA-injected mice displayed dense tumor cell aggregations. Ph-ChNPs and tamoxifen treatments improved histopathological variations, with the combination treatment showing significant apoptosis of tumor cells. This study demonstrates the significant potential of Ph-ChNPs combined with tamoxifen in breast cancer treatment. The combination therapy effectively reduces tumor growth, induces apoptosis and modulates critical breast cancer markers, offering a promising therapeutic strategy.","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"7 3","pages":"68-68"},"PeriodicalIF":0.0,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2624-8549/7/3/68/pdf?version=1745326533","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147331596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tethered Antigenic Suppression Shields the Hemagglutinin Head Domain and Refocuses the Antibody Response to the Stalk Domain. 栓系抗原抑制屏蔽血凝素头部结构域,并将抗体反应重新集中到茎结构域。
IF 2.6
Chemistry-Switzerland Pub Date : 2025-02-01 Epub Date: 2025-01-21 DOI: 10.3390/chemistry7010012
Donguk Kim, Kathryn Loeffler, Yixin Hu, Ammar Arsiwala, Steven Frey, Shruthi Murali, Vivek Hariharan, Alberto Moreno, Ravi S Kane
{"title":"Tethered Antigenic Suppression Shields the Hemagglutinin Head Domain and Refocuses the Antibody Response to the Stalk Domain.","authors":"Donguk Kim, Kathryn Loeffler, Yixin Hu, Ammar Arsiwala, Steven Frey, Shruthi Murali, Vivek Hariharan, Alberto Moreno, Ravi S Kane","doi":"10.3390/chemistry7010012","DOIUrl":"10.3390/chemistry7010012","url":null,"abstract":"<p><p>Influenza has been a global health concern for the past century. Current seasonal influenza vaccines primarily elicit an antibody response that targets the immunodominant head domain of the viral glycoprotein hemagglutinin (HA), which consistently mutates due to selective pressure. To circumvent this problem, we introduce a \"tethered antigenic suppression\" strategy to shield the HA head domain and refocus the immune response towards the conserved but immunosubdominant stalk domain of HA. Specifically, we tethered an antibody fragment (Fab) that recognizes the Sb antigenic site in the HA head domain to the HA protein with a linker. We immunized separate groups of female mice with the Fab-tethered HA or regular HA and characterized the elicited antibody response. We demonstrate that shielding the HA head domain with a tethered Fab suppresses the antibody titers towards all five key antigenic sites in the HA head domain while eliciting a robust anti-stalk antibody response. Our work highlights the potential of tethered antigenic suppression as a strategy to refocus the antibody response towards conserved epitopes on protein antigens.</p>","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"7 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12468577/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145187455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficient Catalytic Hydrogenation of Lignin-Derived Phenolics Under Mild Conditions 温和条件下木质素衍生酚类化合物的高效催化加氢反应
Chemistry-Switzerland Pub Date : 2024-12-12 DOI: 10.3390/chemistry6060098
Yumeng Song, Ping Chen, Hui Lou, Xiaoming Zheng, Xiangen Song
{"title":"Efficient Catalytic Hydrogenation of Lignin-Derived Phenolics Under Mild Conditions","authors":"Yumeng Song, Ping Chen, Hui Lou, Xiaoming Zheng, Xiangen Song","doi":"10.3390/chemistry6060098","DOIUrl":"https://doi.org/10.3390/chemistry6060098","url":null,"abstract":"This paper studies the catalytic hydrogenation reduction of lignin-derived phenolic compounds, such as catechol, guaiacol (O-methoxyphenol), phenol, P-methylphenol, O-ethylphenol, O-ethoxyphenol, etc. The reaction system focuses on the catalytic performance of hydrodeoxygenation reactions involving the phenolic derivatives of the lignin depolymerization products catechol and guaiacol. A series of Al2O3-TiO2 composite oxide supports with different Al/Ti ratios were prepared by a co-precipitation method, and a 5% Pd/Al2O3-TiO2 bifunctional catalyst was prepared by an impregnation method and characterized with XRD, SEM, BET, NH3-TPD, etc. Among these, the Pd/Al2Ti1 catalyst had the most excellent catalytic performance. At 100 °C and 2 MPa hydrogen pressure, the conversion of catechol was as high as 100%, and at 100 °C and 5 MPa hydrogen pressure, the conversion of guaiacol reached 90%.","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"6 6","pages":"1622-1634"},"PeriodicalIF":0.0,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147889037","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Dynamic Magnetic Control of Lanthanide Metal–Organic Framework Crystals and Their Polarized Emissions 镧系金属-有机骨架晶体的动态磁控制及其极化发射
Chemistry-Switzerland Pub Date : 2024-11-14 DOI: 10.3390/chemistry6060084
Bojun Shi, Hao Jia, Lingfang Chen, Shuchun Zhang, Yu Zhang, Baipeng Yin, Shuming Bai, Chuang Zhang
{"title":"Dynamic Magnetic Control of Lanthanide Metal–Organic Framework Crystals and Their Polarized Emissions","authors":"Bojun Shi, Hao Jia, Lingfang Chen, Shuchun Zhang, Yu Zhang, Baipeng Yin, Shuming Bai, Chuang Zhang","doi":"10.3390/chemistry6060084","DOIUrl":"https://doi.org/10.3390/chemistry6060084","url":null,"abstract":"Traditional barcode encoding methods are constrained by the inability to dynamically control crystal orientations, thereby limiting their applications. In this work, we investigate the dynamic magnetic control of lanthanide metal–organic framework crystals and their potential for advancing photonic barcode technology. A paramagnetic fluorescent Eu-MOF microcrystal with sizes ranging from 30 to 40 μm in length and 5 to 10 μm in width was synthesized, and its magnetic orientation and polarized emission were systematically investigated. Eu-MOF crystallizes in an orthorhombic space group, growing along the crystallographic b-axis and ultimately forming an anisotropic cuboid shape. Eu-MOF microcrystals exhibit significant magnetic anisotropy, causing the crystallographic c-axis of the crystal to align with the magnetic field when a uniaxial magnetic field of ~10 mT is applied. Furthermore, the Eu-MOF microcrystal exhibited characteristic Eu emissions with peaks at 594 nm, 616 nm, and 695 nm, and showed a high degree of polarization (DOP), reaching 0.904 at 616 nm. Therefore, the utilization of a rotating magnetic field not only enables precise and dynamic control over the crystal orientations but also results in a significant variation in the luminescence intensity. This capability enabled us to propose an innovative encryption barcode scheme in which the emission intensities of different luminescence peaks are converted into barcode widths, with the sequence of magnetic field directions serving as the encryption key. This approach presents a novel method for data storage and anti-counterfeiting, significantly enhancing the versatility and capacity of photonic barcodes.","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"6 6","pages":"1415-1426"},"PeriodicalIF":0.0,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2624-8549/6/6/84/pdf?version=1731567049","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147896096","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preparation of Hierarchical Porous ZIF-67 and Its Application in Zinc Battery Separator 分级多孔ZIF-67的制备及其在锌电池隔膜中的应用
Chemistry-Switzerland Pub Date : 2024-10-31 DOI: 10.3390/chemistry6060080
Tian Zhao, Jian Yu, Pengcheng Xiao, Saiqun Nie, Shilin Peng, Jiayao Chen, Fuli Luo, Christoph Janiak, Yi Chen
{"title":"Preparation of Hierarchical Porous ZIF-67 and Its Application in Zinc Battery Separator","authors":"Tian Zhao, Jian Yu, Pengcheng Xiao, Saiqun Nie, Shilin Peng, Jiayao Chen, Fuli Luo, Christoph Janiak, Yi Chen","doi":"10.3390/chemistry6060080","DOIUrl":"https://doi.org/10.3390/chemistry6060080","url":null,"abstract":"This study successfully prepared a hierarchically porous ZIF-67 (H-ZIF-67) by incorporating the polyvinylpyrrolidone (PVP) at room temperature. Compared to standard control ZIF-67 (C-ZIF-67) with a yield of 81% and a BET specific surface area of 1228 m2·g−1, the H-ZIF-67 not only exhibited improved crystallinity and pore structure but also achieved a yield of up to 93% and a BET specific surface area of 1457 m2·g−1. Due to its hierarchically porous structure, H-ZIF-67 demonstrated excellent adsorption capacity and efficiency for methylene orange (MO). Additionally, the composite separator created by combining H-ZIF-67 with nanocellulose (CNF) exhibited remarkable uniformity and dispersion in zinc batteries. In comparison to a conventional CNF separator, the porous structure and high specific surface area of H-ZIF-67 significantly enhanced its electrolyte wettability and Zn2+ transport rates. Its abundant Lewis acid sites effectively promoted the uniform deposition of Zn2+, thereby suppressing the formation of zinc dendrites and improving the cycling and safety performance of zinc-ion batteries. Experimental results indicate that the ion conductivity of the membrane was 4.31 mS·cm−1, the electrolyte absorption rate was 316%, and it could cycle stable for over 4000 h at a current density of 1 mA·cm−2 with a discharge capacity of 1 mAh·cm−2. This achievement will open up new avenues for the preparation and application of ZIF-67 composite separators in aqueous zinc-ion batteries.","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"6 6","pages":"1363-1373"},"PeriodicalIF":0.0,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2624-8549/6/6/80/pdf?version=1730689547","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147907256","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
An Alternative Method for Synthesizing N,2,3-Trimethyl-2H-indazol-6-amine as a Key Component in the Preparation of Pazopanib 制备帕唑帕尼关键组分N,2,3-三甲基- 2h -茚唑-6-胺的替代方法
Chemistry-Switzerland Pub Date : 2024-09-19 DOI: 10.3390/chemistry6050063
Thi Thanh Cham Bui, Hue Linh Luu, Thanh Thi Luong, Thị Ngọc Anh Nguyễn, Nguyệt Sương Huyền Đào, Van Giang Nguyen, Đình Luyện Nguyễn, Nguyen Trieu Trinh, Van Hai Nguyen
{"title":"An Alternative Method for Synthesizing N,2,3-Trimethyl-2H-indazol-6-amine as a Key Component in the Preparation of Pazopanib","authors":"Thi Thanh Cham Bui, Hue Linh Luu, Thanh Thi Luong, Thị Ngọc Anh Nguyễn, Nguyệt Sương Huyền Đào, Van Giang Nguyen, Đình Luyện Nguyễn, Nguyen Trieu Trinh, Van Hai Nguyen","doi":"10.3390/chemistry6050063","DOIUrl":"https://doi.org/10.3390/chemistry6050063","url":null,"abstract":"Due to its application as an anti-cancer drug, pazopanib (1) has attracted the interest of many researchers, and several studies on pazopanib synthesis have been reported over the years. This paper provides a novel route for synthesizing N,2,3-trimethyl-2H-indazol-6-amine (5), which is a crucial building block in the synthesis of pazopanib from 3-methyl-6-nitro-1H-indazole (6). By alternating between the reduction and two methylation steps, compound 5 was obtained in a yield comparable (55%) to what has been reported (54%). It is noteworthy that the last step of N2-methylation also yielded N,N,2,3-tetramethyl-2H-indazol-6-amine (5′) as a novel compound. Furthermore, the data presented in this paper can serve as a valuable resource for future research aimed at further refining the process of synthesizing pazopanib and its derivatives.","PeriodicalId":53216,"journal":{"name":"Chemistry-Switzerland","volume":"6 5","pages":"1089-1098"},"PeriodicalIF":0.0,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/2624-8549/6/5/63/pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147918936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
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