959558-50-0

Usage

Uses

Used in Medicinal Chemistry:
4-Iodo-2,7-naphthyridin-1... is used as a key intermediate in the synthesis of pharmaceutical drugs and bioactive molecules. Its iodo substitution allows for further functionalization and modification, leading to the development of more complex and diverse compounds with potential biological activities.
Used in Organic Synthesis:
In the field of organic synthesis, 4-Iodo-2,7-naphthyridin-1... serves as a valuable precursor for creating a wide range of complex and diverse compounds. Its unique structure and reactivity enable the synthesis of novel compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
4-Iodo-2,7-naphthyridin-1... is utilized in research and development for exploring its potential applications in various scientific fields. Its unique structure and chemical properties make it an interesting target for further investigation, leading to the discovery of new compounds and applications.
Overall, 4-Iodo-2,7-naphthyridin-1... is a promising chemical compound with a wide range of applications in chemistry and pharmaceutical research, making it a valuable asset for the development of innovative products and solutions.

Upstream product

• 33402-75-4 4-methylnicotinic acid methyl ester 
• 67988-50-5 2,7-naphthyridinyl-1(2H)-one 

Downstream Products

• 1234616-02-4 1-chloro-4-iodo-2,7-diazanaphthalene 
• 1345044-53-2 1-chloro-4-phenyl-[2,7]naphthyridine 
• 2306193-61-1 (2S,4R)-N-(2-((5-(4-(2,6-dimethoxy-4-(2-methyl-1-oxo-1,2-dihydro-2,7-naphthyridin-4-yl)benzyl)piperazin-1-yl)pentyl)oxy)-4-(4-methylthiazol-5-yl)benzyl)-1-((S)-2-(1-fluorocyclopropane-1-carboxamido)-3,3-dimethylbutanoyl)-4-hydroxypyrrolidine-2-carboxamide 
• 2306193-61-1 (2S,4S)-N-(2-((5-(4-(2,6-dimethoxy-4-(2-methyl-1-oxo-1,2-dihydro-2,7-naphthyridin-4-yl)benzyl)piperazin-1-yl)pentyl)oxy)-4-(4-methylthiazol-5-yl)benzyl)-1-((S)-2-(1-fluorocyclopropane-1-carboxamido)-3,3-dimethylbutanoyl)-4-hydroxypyrrolidine-2-carboxamide 
• 1616401-76-3 2-benzyl-4-(3,5-dimethylisoxazol-4-yl)-2,7-naphthyridin-1(2H)-one 
• 1616403-12-3 2-benzyl-4-iodo-2,7-naphthyridin-1(2H)-one 
• 1353968-43-0 2-(5-chloro-2-fluoro-phenyl)-4-[1-(2-morpholin-4-yl-ethoxy)-[2,7]naphthyridin-4-yl]-[1,8]naphthyridine 
• 1353968-39-4 4-[2-(5-chloro-2-fluoro-phenyl)-[1,8]naphthyridin-4-yl]-2-(2-morpholin-4-yl-ethyl)-2H-[2,7]naphthyridin-1-one 
• 1353968-26-9 4-[2-(5-chloro-2-fluoro-phenyl)-[1,8]naphthyridin-4-yl]-2-(2-hydroxy-ethyl)-2H-[2,7]naphthyridin-1-one 

Relevant academic research and scientific papers

Pyrido/pyridazocyclic compound and application thereof

The invention discloses a pyrido/pyridazocyclic compound, a pharmaceutically acceptable salt and a solvent compound thereof. The invention further provides a preparation method of the compound, a composition with the compound and application of the compound for preparing medicines for treating diseases or disorders related to EED (embryonic ectoderm development) protein and/or PRC2 (polycomb repressive complex 2) protein composition action mechanisms.

Preparation of Polyfunctional Naphthyridines by Cobalt-Catalyzed Cross-Couplings of Halogenated Naphthyridines with Magnesium and Zinc Organometallics

CoCl2 (5%) catalyzes cross-couplings of various halogenated naphthyridines with alkyl- and arylmagnesium halides. Also, arylzinc halides undergo smooth cross-couplings with various naphthyridines in the presence of CoCl2·2LiCl (5%) a