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Synthesis of spiro[pyrazolo[3,4-b] pyridine-4,3′-indoline] and spiro [benzo[h]pyrazolo[3,4-b]quinoline-4,3′-indoline] derivatives using wet cyanuric chloride under solvent-free conditionS

Zhikui Yin, +2 more
- 19 Jun 2013 - 
- Vol. 125, Iss: 3, pp 601-606
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TLDR
In this article, a simple and efficient synthesis of spiro[pyrazolo[3,4-b]pyridine-4,3′-indoline] and spiro [benzo[h] pyrazolo [3, 4-b]-quinoline- 4, 3′indoline derivatives has been accomplished by the one-pot condensation of isatins, 3-methyl-1-phenyl-1H-pyrazol-5-amine and Meldrum's acid or 2-hydroxy-1, 4n
Abstract
A simple and efficient synthesis of spiro[pyrazolo[3,4-b]pyridine-4,3′-indoline] and spiro[benzo[h] pyrazolo[3,4-b]quinoline-4,3′-indoline] derivatives has been accomplished by the one-pot condensation of isatins, 3-methyl-1-phenyl-1H-pyrazol-5- amine and Meldrum’s acid or 2-hydroxy-1,4-naphthoquinone in the presence of wet cyanuric chloride as a catalyst under solvent-free conditions.

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Multicomponent Dipolar Cycloaddition Strategy: Combinatorial Synthesis of Novel Spiro-Tethered Pyrazolo[3,4-b]quinoline Hybrid Heterocycles

TL;DR: The stereoselective syntheses of a library of novel spiro-tethered pyrazolo[3,4-b]quinoline-pyrrolidine/ pyrrolothiazole/indolizine-oxindole/acenaphthene hybrid heterocycles have been achieved through the 1,3-dipolar cycloaddition of azomethine ylides generated in situ from α-amino acids and 1,2-d
Journal ArticleDOI

The catalyst-free syntheses of pyrazolo[3,4-b]quinolin-5-one and pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidin-5,7-dione derivatives by one-pot, three-component reactions

TL;DR: In this article, the synthesis of tricyclic pyrazolo[3,4- b ]quinolin-5-one and pyrido[2,3- d ]pyrimidin-5,7-dione derivatives by cyclocondensation was reported.
Journal ArticleDOI

Use of 2,4,6-trichloro-1,3,5-triazine (TCT) as organic catalyst in organic synthesis

TL;DR: In recent years, 2,4,6-trichloro-1,3,5-triazine (TCT, cyanuric chloride) has been used as organic catalyst in many organic synthesis, because it is stable, nonvolatile, inexpensive, commercially available, and easy to handle.
References
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Journal ArticleDOI

Multiple-Component Condensation Strategies for Combinatorial Library Synthesis

TL;DR: This Account focuses on multiple-component condensations (MCCs) as one subset of strategies for the generation of compound libraries, and it is instructive to contrast this approach with linear synthesis to highlight the differences in methods, potential library size, and output format.
Journal ArticleDOI

Paraherquamides, brevianamides, and asperparalines: laboratory synthesis and biosynthesis. An interim report.

TL;DR: Key biosynthetic studies are described, along with classical synthetic approaches as well as those inspired by Nature for the synthesis of these interesting molecules.
Journal ArticleDOI

Recent advances in multicomponent reactions for diversity-oriented synthesis

TL;DR: This review will highlight recent developments in MCRs as a rich source of molecular diversity as well as the discovery of new reactions, development of the first asymmetric catalysts, and the application of M CRs to natural products and other targets of biological interest.
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