ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-methoxy-1,5-naphthyridine-3-carboxylate

Base Information

Chemical Name:ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-methoxy-1,5-naphthyridine-3-carboxylate
CAS No.:1310359-75-1
Molecular Formula:C₁₉H₁₄ClF₃N₂O₃
Molecular Weight:410.78
Hs Code.:

Synonyms:ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-methoxy-1,5-naphthyridine-3-carboxylate

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Chemical Property of ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-methoxy-1,5-naphthyridine-3-carboxylate

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Technology Process of ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-methoxy-1,5-naphthyridine-3-carboxylate

There total 1 articles about ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-methoxy-1,5-naphthyridine-3-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: 182344-18-9
2-chloro-5-(trifluoromethyl)phenylboronic acid

: 724788-64-1
ethyl 4-bromo-6-methoxy-1,5-naphthyridine-3-carboxylate

: 1310359-75-1
ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-methoxy-1,5-naphthyridine-3-carboxylate

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium carbonate; In 1,4-dioxane; water; for 2h; Reflux;
DOI:10.1021/jo200824b

Reference yield: 92.0%

: 1310359-75-1
ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-methoxy-1,5-naphthyridine-3-carboxylate

: 1310359-87-5
ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-oxo-5,6-dihydro-1,5-naphthyridine-3-carboxylate

Guidance literature:: ethyl 4-[2-chloro-5-(trifluoromethyl)phenyl]-6-methoxy-1,5-naphthyridine-3-carboxylate; With chloro-trimethyl-silane; sodium iodide; In acetonitrile; Reflux;

With water; In acetonitrile;
DOI:10.1021/jo200824b