ethyl 8-[3-fluoro-4-(2-{2-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]ethoxy}ethoxy)phenyl]-1,6-naphthyridine-2-carboxylate

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Chemical Name:ethyl 8-[3-fluoro-4-(2-{2-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]ethoxy}ethoxy)phenyl]-1,6-naphthyridine-2-carboxylate
CAS No.:1248555-75-0
Molecular Formula:C₂₈H₃₃FN₂O₇
Molecular Weight:528.578
Hs Code.:

Synonyms:ethyl 8-[3-fluoro-4-(2-{2-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]ethoxy}ethoxy)phenyl]-1,6-naphthyridine-2-carboxylate

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Chemical Property of ethyl 8-[3-fluoro-4-(2-{2-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]ethoxy}ethoxy)phenyl]-1,6-naphthyridine-2-carboxylate

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Technology Process of ethyl 8-[3-fluoro-4-(2-{2-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]ethoxy}ethoxy)phenyl]-1,6-naphthyridine-2-carboxylate

There total 4 articles about ethyl 8-[3-fluoro-4-(2-{2-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]ethoxy}ethoxy)phenyl]-1,6-naphthyridine-2-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: 70.0%

: 1248555-73-8
ethyl 8-(3-fluoro-4-hydroxyphenyl)-1,6-naphthyridine-2-carboxylate

: 60221-37-6
8-(1H-tetrahydropyran-2-yloxy)-3n₆³-dioxaoctan-1-ol

: 1248555-75-0
ethyl 8-[3-fluoro-4-(2-{2-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]ethoxy}ethoxy)phenyl]-1,6-naphthyridine-2-carboxylate

Guidance literature:: With cyanomethylenetributyl-phosphorane; In toluene; at 80 ℃; for 1h; Inert atmosphere;

Reference yield:

: 2105-94-4
4-bromo-2-fluorophenol

: 1248555-75-0
ethyl 8-[3-fluoro-4-(2-{2-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]ethoxy}ethoxy)phenyl]-1,6-naphthyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetone / 2 h / 20 °C

2.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / dimethyl sulfoxide / 1 h / 80 °C

3.1: potassium carbonate / bis-triphenylphosphine-palladium(II) chloride / ethanol; water / 1 h / 90 °C / Inert atmosphere

3.2: 0.75 h / 90 °C

4.1: cyanomethylenetributyl-phosphorane / toluene / 1 h / 80 °C / Inert atmosphere

With potassium acetate; potassium carbonate; cyanomethylenetributyl-phosphorane; bis-triphenylphosphine-palladium(II) chloride; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In ethanol; water; dimethyl sulfoxide; acetone; toluene; 3.1: Suzuki Coupling / 4.1: Mitsunobu reaction;

Reference yield:

: 143610-62-2
4-bromo-2-fluoro-1-methoxymethoxybenzene

: 1248555-75-0
ethyl 8-[3-fluoro-4-(2-{2-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]ethoxy}ethoxy)phenyl]-1,6-naphthyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / dimethyl sulfoxide / 1 h / 80 °C

2.1: potassium carbonate / bis-triphenylphosphine-palladium(II) chloride / ethanol; water / 1 h / 90 °C / Inert atmosphere

2.2: 0.75 h / 90 °C

3.1: cyanomethylenetributyl-phosphorane / toluene / 1 h / 80 °C / Inert atmosphere

With potassium acetate; potassium carbonate; cyanomethylenetributyl-phosphorane; bis-triphenylphosphine-palladium(II) chloride; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In ethanol; water; dimethyl sulfoxide; toluene; 2.1: Suzuki Coupling / 3.1: Mitsunobu reaction;