59997-14-7

Usage

Uses

Used in Medicinal Chemistry:
10-ethyl-3-methylpyrimido[4,5-b]quinoline-2,4(3H,10H)-dione is used as a potential candidate for the development of novel drugs and pharmaceuticals due to its unique molecular structure and potential applications in medicinal chemistry.
Further research is needed to fully understand the specific properties and uses of this chemical compound in various fields.

Upstream product

• 4017-00-9 o-(N-ethyl)aminobenzyl alcohol 
• 4318-56-3 3-methyl-6-chlorouracil 
• 80885-70-7 C₁₄H₁₃N₃O₃ 

Downstream Products

• 137347-74-1 10-Ethyl-3-methyl-5-phenethylamino-10H-pyrimido[4,5-b]quinoline-2,4-dione 
• 67984-95-6 1-ethyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid 
• 80885-75-2 3-hydroxy-1-ethylquinolin-2(1H)-one 
• 37942-07-7 3,5-di-tert-butyl-2-hydroxybenzaldehyde 
• 100-52-7 benzaldehyde 

Relevant academic research and scientific papers

A new synthetic approach to 5-deazaflavin and 5-deaza-10-thiaflavin

A novel, one-step synthesis of 5-deazaflavin was developed, in which a [4 + 2]cycloaddition is presumably involved, to give the 5-deazaflavin derivative in moderate yield. This methodology was successfully applied to the stepwise preparation of its thio a

A New Synthetic Method for the Preparation of 5-Deazaflavins and 5-Deaza-10-oxaflavins

The condensation of 6-chlorouracils with o-(substituted amino)benzyl alcohols and o-hydroxybenzyl alcohol gave directly 5-deazaflavin and 5-deaza-10-oxaflavin derivatives, respectively.

REACTIVITY OF 4a,5-EPOXY-5-DEAZAFLAVINS

Reactions of 4a,5-epoxy-5-deazaflavins with aqueous potassium carbonate, Vilsmeier reagent (dimethylformamide-phosphorus oxychloride), acetic anhydride-acetic acid, pyridine and triethanolamine gave the corresponding oxazolonoquinolines, 5-chloro-5-deazaflavins, 4a,5-diacetoxy-5-deazaflavins, l,5-dihydro-5-deazaflavin-5-ones, and deoxygenated 5-deazaflavins, respectively.