70292-64-7Relevant academic research and scientific papers
Cs2CO3-Promoted C?O Coupling Protocol Enables Solventless (Hetero)aryl Ether Synthesis under Air Atmosphere
Jiang, Bowen,Chen, Cheng,Fan, Guang-Gao,Sang, Wei,Cheng, Hua,Zhang, Rui,Yuan, Ye,Li, Qi-Zhong,Verpoort, Francis
supporting information, (2022/02/05)
In this work, a Cs2CO3-promoted synthetic approach was identified for (hetero)aryl ether synthesis via the C?O coupling of various (hetero)aryl chlorides and alcohols/phenol. To our delight, the reactions could be carried out under transition-metal-free and solvent-free conditions. Moreover, analytical-grade reagents and air atmosphere were readily tolerated. To showcase the practical usefulness of the present protocol, the assembly of a bioactive molecule was facilely realized and the gram-scale production of selected ether products was also efficiently accomplished. In addition, density functional theory (DFT) studies, along with a few mechanistic experiments, were conducted to elucidate a proposed reaction pathway and rationalize the pivotal role of Cs2CO3 in promoting this process. Hopefully, this work could provide useful information for researchers who are engaging in C?O cross-coupling reactions.
Syntheses of benzo[d]thiazol-2(3H)-one derivatives and their antidepressant and anticonvulsant effects
Jin, Qinghao,Fu, Zhiyang,Guan, Liping,Jiang, Haiying
, (2019/07/31)
Thirty-four new benzo[d]thiazol derivatives 2a–2i, 3a–3r, and 4a–4g were synthesized and investigated for their potential antidepressant and anticonvulsant effects. In a forced swimming test, 2c and 2d showed the highest antidepressant and anticonvulsant
Copper(I)-catalyzed cascade synthesis of 2-substituted 1,3-benzothiazoles: Direct access to benzothiazolones
Murru, Siva,Mondal, Pravat,Yella, Ramesh,Patel, Bhisma K.
experimental part, p. 5406 - 5413 (2010/02/28)
An efficient cascade process for the preparation of 2-substituted 1,3-benzothiazoles directly from 2-haloaryl isothiocyanates and O or S nucleophiles by a Cu-catalyzed, intramolecular, C-S bond formation has been developed. This cascade method is viable f
Process for synthesizing thiacyanine dyes
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, (2008/06/13)
There is described a process for synthesizing a thiacyanine dye wherein a 2-halo, 2-alkoxy or 2-aryloxybenzothiazole is alkylated by a strong alkylating agent to form a quaternized benzothiazole which, without being isolated, is condensed with a benzothiazolium betaine in a nonaqueous homogeneous medium. The thiacyanine dye is useful for enhancing the photosensitivity of a blue-sensitive silver halide emulsion.
