69407-71-2

Usage

Uses

Used in Pharmaceutical Research:
Ethyl 1-allyl-4-hydroxy-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate is used as a research compound for exploring its potential biological activity and therapeutic applications. The presence of hydroxy and allyl groups indicates that it may interact with biological systems, warranting further investigation into its effects on various diseases and conditions.
Used in Drug Development:
In the field of drug development, ethyl 1-allyl-4-hydroxy-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate is utilized as a starting material or a structural component in the synthesis of new pharmaceutical agents. Its unique chemical features may contribute to the discovery of novel drugs with improved efficacy and selectivity.

Upstream product

• 78997-37-2 2-allylamino-6-methylnicotinic acid methyl ester 
• 36239-09-5 ethyl chlorocarbonylacetate 
• 97484-82-7 1-allyl-7-methyl-2H-pyrido<2,3-d><1,3>oxazine-2,4(1H)-dione 
• 105-53-3 diethyl malonate 
• 53277-47-7 2-chloro-6-methylnicotinic acid methyl ester 
• 28900-10-9 2-chloro-6-methylnicotinonitrile 
• 97484-92-9 2-allylamino-6-methyl-3-pyridinecarbonitrile 
• 97484-94-1 2-allylamino-6-methylnicotinic acid sodium salt 
• 55552-69-7 2-ethylmalonyl dichloride 

Relevant academic research and scientific papers

2-Oxo-1,8-naphthyridine-3-carboxylic Acid Derivatives with Potent Gastric Antisecretory Properties

The syntheses of 2-oxo-1,8-naphthyridine-3-carboxylic acid derivatives having potent gastric antisecretory properties in the pyloric-ligated (Shay) rat model are described.Two of the more potent compounds tested that were selected for more detailed dose-r

The Chemistry of 3-Azaisatoic Anhydrides. Synthesis and Reactions of Polyaza Heterocycles

The preparation of a variety of N-substituted 3-azaisotoic anhydrides 3 and 8 is described.These anhydrides reacted with thiopseudoureas to give interesting bicyclic, tricyclic, and tetracyclic heterocycles many of which are new ring systems.One such hete

4-Amino-3-carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives

4-Amino-3-carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives are anti-secretory agents for use in the treatment of peptic ulcer disease.

Antisecretory 4-oxy-3-carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives

Substituted 4-oxy-3-carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives as gastric antisecretory agents for use in the treatment of peptic ulcer disease.

4-Hydroxy-pyrido[2,3-b]pyridine-2(1H)-one-3-carboxylic acids and esters

Anti-allergic 4-hydroxy-pyrido[2,3-b]pyridine-2(1H)-one-3-carboxylic acids and esters are prepared by reacting a 3,4-dihydro-1,3-dioxo-1H-pyrido[2,3-d][1,3]oxazine (a 3-azaisatoic anhydride) with an alkali metal salt of a malonic ester.