86814-97-3

Usage

Chemical structure

1,3-dimethyl-1,7-dihydropyrano[4,3-b]pyrrole-4,6-dione has a complex molecular structure with a pyranopyrrole ring and two methyl groups attached to the 1 and 3 positions of the ring.

Biological activities

The compound has potential biological activities, which make it a subject of interest for further research.

Therapeutic properties

It has been studied for its potential as an antifungal and anticancer agent, indicating its potential use in the development of new treatments for these conditions.

Medicinal chemistry

The unique structure of 1,3-dimethyl-1,7-dihydropyrano[4,3-b]pyrrole-4,6-dione makes it an interesting target for further research in the field of medicinal chemistry.

Drug development

The compound's potential therapeutic properties and unique structure make it a promising candidate for drug development, particularly in the areas of antifungal and anticancer treatments.

Molecule type

1,3-dimethyl-1,7-dihydropyrano[4,3-b]pyrrole-4,6-dione is an organic compound, specifically a heterocyclic compound due to the presence of multiple heteroatoms in its structure.

Potential applications

Due to its antifungal and anticancer properties, 1,3-dimethyl-1,7-dihydropyrano[4,3-b]pyrrole-4,6-dione may be used in the development of new pharmaceuticals for the treatment of fungal infections and cancer.

Research focus

Further research on 1,3-dimethyl-1,7-dihydropyrano[4,3-b]pyrrole-4,6-dione may focus on understanding its mechanism of action, optimizing its structure for improved efficacy, and evaluating its safety and potential side effects.

Structural complexity

The complex structure of 1,3-dimethyl-1,7-dihydropyrano[4,3-b]pyrrole-4,6-dione presents challenges in synthesis and characterization, but also offers opportunities for the development of novel therapeutic agents.

Upstream product

• 33369-26-5 1,4-dimethyl-3-carbethoxy-pyrrole-2-acetic acid ethyl ester 
• 105-50-0 diethyl 1,3-acetonedicarboxylate 
• 33369-45-8 3-carboxy-1,4-dimethyl-1H-pyrrole-2-acetic acid 
• 108-24-7 acetic anhydride 

Relevant academic research and scientific papers

Catalytic asymmetric tamura cycloadditions

In the presence of a novel, tert-butyl-substituted squaramide-based catalyst, enolizable anhydrides react with alkylidene oxindoles to generate spirooxindole products of significant synthetic interest with excellent enantio- and diastereocontrol. The methodology is of wide scope and encompasses both homophthalic and glutaconic anhydride derivatives, which lead to structurally diverse products. Glutaconic acid-derived anhydrides undergo a clean post-cyclization decarboxylation process which is not a feature of reactions involving homophthalic acid-derived anhydrides. The unusual influence of reaction temperature on diastereocontrol has been probed, with reactions occurring at 30 °C and -30 °C delivering products epimeric at one stereocenter only, in near optical purity. Squared away: The first strategy for bringing about enantioselective Tamura reactions is reported. In the presence of a squaramide-based catalyst, enolizable anhydrides react with alkylidene oxindoles to generate spirooxindole products with excellent enantio- and diastereocontrol. The methodology is of wide scope and leads to structurally diverse products.

Regioselective Acetylation of some N-Methylpyrrole Derivatives with Isopropenyl Acetate and Different Acetic Anhydrides

We studied the reactions of some N-methylpyrrole derivatives with isopropenyl acetate and different acetic anhydrides.We have found that the reaction with isopropenyl acetate afforded 5-acetylpyrrole derivatives while with acetic anhydrides acetylation oc

Facile and Efficient Syntheses of Carboxylic Anhydrides and Amides Using (Trimethylsilyl)ethoxyacetylene

(Trimethylsilyl)ethoxyacetylene, a stable and easy-handling reagent, serves as an excellent dehydrating agent for the synthesis of carboxylic anhydrides and amides from the corresponding carboxylic acids.By means of this reagent, various types of acid-sensitive carboxylic anhydrides and amides were obtained almost in quantative yields.Twenty-two examples of carboxylic anhydrides and 12 examples of amides were presented.

A MILD AND FACILE SYNTHESIS OF CARBOXYLIC ANHYDRIDES

Reaction of carboxylic acids with trimethylsilylethoxyacetylene in an inert solvent under mild conditions affords the corresponding carboxylic anhydrides in almost quantitative yields.