Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Synthesis of 3-Alkyl-5-(diethylaminomethyl)-1-(1,3-thiazole)pyrazoles

View through CrossRef
By the reaction of 3-alkyl-5-(diethylaminomethyl) pyrazoles with chloroanhydride of monochloroacetic acid, the pyrazoles with chloromethyl carbonyl substituent have been synthesized. Due to presence of reactive COCH2Cl groups in a molecule, the pyrazoles have been subjected to heterocyclization with thicarbamides (thiobenzamide, thicarbamide and phenylthiocarbamide) in the presence of triethyleamine in a medium of ethanol, as a result of which the previously unknown 3-alkyl-5-diethylaminomethyl-1-(1,3-thiazol)substituted pyrazole derivatives have been obtained.
Title: Synthesis of 3-Alkyl-5-(diethylaminomethyl)-1-(1,3-thiazole)pyrazoles
Description:
By the reaction of 3-alkyl-5-(diethylaminomethyl) pyrazoles with chloroanhydride of monochloroacetic acid, the pyrazoles with chloromethyl carbonyl substituent have been synthesized.
Due to presence of reactive COCH2Cl groups in a molecule, the pyrazoles have been subjected to heterocyclization with thicarbamides (thiobenzamide, thicarbamide and phenylthiocarbamide) in the presence of triethyleamine in a medium of ethanol, as a result of which the previously unknown 3-alkyl-5-diethylaminomethyl-1-(1,3-thiazol)substituted pyrazole derivatives have been obtained.

Related Results

Thiazole-Based Antioxidants: Pioneering a Decade of Therapeutic Advances
Thiazole-Based Antioxidants: Pioneering a Decade of Therapeutic Advances
Background:: Thiazole-based compounds have attracted considerable interest due to their potent antioxidant abilities, which are crucial for combating diseases a...
Thiazoles in glycosylation reactions: Novel synthesis of thiazole thioglycosides
Thiazoles in glycosylation reactions: Novel synthesis of thiazole thioglycosides
AbstractThis research reports a novel method for synthesizing new thiazole thioglycosides. This series of thiazole thioglycosides were designed by the reaction of potassium cyanoca...
Synthetic and Medicinal Perspective of Fused-Thiazoles as Anticancer Agents
Synthetic and Medicinal Perspective of Fused-Thiazoles as Anticancer Agents
Background:Cancer is second leading disease after cardiovascular disease. Presently, Chemotherapy, Radiotherapy and use of chemicals are some treatments available these days. Thiaz...
THIAZOLE DERIVATIVES AS POTENTIAL ANTIDIABETIC AGENTS
THIAZOLE DERIVATIVES AS POTENTIAL ANTIDIABETIC AGENTS
Various molecules showing pharmacological activities consist of thiazole as a core structure having heteroatom as sulfur and nitrogen. Thiazole is present in many naturally occurri...
Synthesis, Characterization, and Antioxidant Activity Evaluation of New N-Methyl Substituted Thiazole-Derived Polyphenolic Compounds
Synthesis, Characterization, and Antioxidant Activity Evaluation of New N-Methyl Substituted Thiazole-Derived Polyphenolic Compounds
Reactive oxygen species play a significant role in various pathological conditions, driving the need for novel, potent antioxidants. While polyphenols are known for their antioxida...
Synthesis of tubuvaline utilizing Mn-mediated radical addition conditions modified for compatibility with heteroaromatics
Synthesis of tubuvaline utilizing Mn-mediated radical addition conditions modified for compatibility with heteroaromatics
The Mn-mediated radical addition reaction developed by our group can synthesize chiral amine substructure with excellent diatereoselectivity. Such methodology was applied in the to...
Wurtz Synthesis
Wurtz Synthesis
Abstract This reaction is a sodium‐mediated coupling of two alkyl halides into a higher order of hydrocarbon and is generally known as the Wurtz synthesis. Analogously, t...
Enamines in Heterocyclic Synthesis: A Route to 4-Substituted Pyrazoles and Condensed Pyrazoles
Enamines in Heterocyclic Synthesis: A Route to 4-Substituted Pyrazoles and Condensed Pyrazoles
Abstract The reaction of nitrile imines, generated in situ, from hydrazonoyl halides 3a - e with enamines 2a - c affords pyrazoles 8a - g. These pyrazoles have been ...

Back to Top