1-(2,4-dimethoxy-benzyl)-6-fluoro-7-pyrrolidin-1-yl-1H-[1,8]naphthyridin-4-one

Base Information

• Chemical Name: 1-(2,4-dimethoxy-benzyl)-6-fluoro-7-pyrrolidin-1-yl-1H-[1,8]naphthyridin-4-one
• CAS No.: 779343-25-8
• Molecular Formula: C₂₁H₂₂FN₃O₃
• Molecular Weight: 383.422
• Mol file: 779343-25-8.mol

Synonyms:1-(2,4-dimethoxy-benzyl)-6-fluoro-7-pyrrolidin-1-yl-1H-[1,8]naphthyridin-4-one

Chemical Property of 1-(2,4-dimethoxy-benzyl)-6-fluoro-7-pyrrolidin-1-yl-1H-[1,8]naphthyridin-4-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(2,4-dimethoxy-benzyl)-6-fluoro-7-pyrrolidin-1-yl-1H-[1,8]naphthyridin-4-one

There total 5 articles about 1-(2,4-dimethoxy-benzyl)-6-fluoro-7-pyrrolidin-1-yl-1H-[1,8]naphthyridin-4-one 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: 88.0%

1-(2,4-dimethoxybenzyl)-6-fluoro-4-oxo-7-pyrrolidin-1-yl-1,4-dihydro-1,8-naphthyridine-3-carboxylic Acid (779337-66-5) → 1-(2,4-dimethoxy-benzyl)-6-fluoro-7-pyrrolidin-1-yl-1H-[1,8]naphthyridin-4-one (779343-25-8)

Guidance literature:

With quinoline; copper(I) oxide; at 180 ℃; for 20h;

DOI:10.1016/j.bmcl.2004.03.091

Reference yield:

2,4-Dimethoxybenzylamine (20781-20-8) → 1-(2,4-dimethoxy-benzyl)-6-fluoro-7-pyrrolidin-1-yl-1H-[1,8]naphthyridin-4-one (779343-25-8)

Guidance literature:

Multi-step reaction with 5 steps

1: CH₂Cl₂ / 3 h / 25 °C

2: K₂CO₃ / acetonitrile / 16 h / Heating

3: K₂CO₃ / CH₂Cl₂ / 16 h / 25 °C

4: aq. LiOH / ethanol / 60 °C

5: 88 percent / Cu₂O; quinoline / 20 h / 180 °C

With quinoline; copper(I) oxide; lithium hydroxide; potassium carbonate; In ethanol; dichloromethane; acetonitrile;

DOI:10.1016/j.bmcl.2004.03.091

Reference yield:

2,6-dichloro-α-(ethoxymethylene)-5-fluoro-β-oxo-3-pyridinepropanoic acid ethyl ester (96568-05-7) → 1-(2,4-dimethoxy-benzyl)-6-fluoro-7-pyrrolidin-1-yl-1H-[1,8]naphthyridin-4-one (779343-25-8)

Guidance literature:

Multi-step reaction with 5 steps

1: CH₂Cl₂ / 3 h / 25 °C

2: K₂CO₃ / acetonitrile / 16 h / Heating

3: K₂CO₃ / CH₂Cl₂ / 16 h / 25 °C

4: aq. LiOH / ethanol / 60 °C

5: 88 percent / Cu₂O; quinoline / 20 h / 180 °C

With quinoline; copper(I) oxide; lithium hydroxide; potassium carbonate; In ethanol; dichloromethane; acetonitrile;

DOI:10.1016/j.bmcl.2004.03.091

upstream raw materials:

1-(2,4-dimethoxybenzyl)-6-fluoro-4-oxo-7-pyrrolidin-1-yl-1,4-dihydro-1,8-naphthyridine-3-carboxylic Acid

2,4-Dimethoxybenzylamine

2,6-dichloro-α-(ethoxymethylene)-5-fluoro-β-oxo-3-pyridinepropanoic acid ethyl ester

7-chloro-1-(2,4-dimethoxybenzyl)-6-fluoro-4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxylic acid ethyl ester