7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-4-fluoro-2-methylphenyl)-1-isopropyl-1,6-naphthyridin-2(1H)-one

Base Information

Chemical Name:7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-4-fluoro-2-methylphenyl)-1-isopropyl-1,6-naphthyridin-2(1H)-one
CAS No.:1442470-60-1
Molecular Formula:C₂₇H₂₉FN₄O₂
Molecular Weight:460.551
Hs Code.:

Synonyms:7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-4-fluoro-2-methylphenyl)-1-isopropyl-1,6-naphthyridin-2(1H)-one

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Chemical Property of 7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-4-fluoro-2-methylphenyl)-1-isopropyl-1,6-naphthyridin-2(1H)-one

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Technology Process of 7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-4-fluoro-2-methylphenyl)-1-isopropyl-1,6-naphthyridin-2(1H)-one

There total 6 articles about 7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-4-fluoro-2-methylphenyl)-1-isopropyl-1,6-naphthyridin-2(1H)-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: 76.9%

: 702-24-9
4-methoxy-N-methylbenzylamine

: 1442470-59-8
3-(5-amino-4-fluoro-2-methylphenyl)-7-chloro-1-isopropyl-1,6-naphthyridin-2(1H)-one

: 1442470-60-1
7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-4-fluoro-2-methylphenyl)-1-isopropyl-1,6-naphthyridin-2(1H)-one

Guidance literature:: at 180 ℃; for 8h; Inert atmosphere;

Reference yield:

: 407640-40-8
2-(4-fluoro-2-methylphenyl)acetic acid

: 1442470-60-1
7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-4-fluoro-2-methylphenyl)-1-isopropyl-1,6-naphthyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: nitric acid / 0.25 h / -15 - 5 °C

2: sulfuric acid / 2.5 h / 85 °C

3: palladium 10% on activated carbon; hydrogen / ethanol / 2 h / 2660.18 Torr

4: caesium carbonate / N,N-dimethyl-formamide / 100 °C

5: trifluoroacetic acid / acetic acid / 8 h / 180 °C / Inert atmosphere

With sulfuric acid; palladium 10% on activated carbon; hydrogen; nitric acid; caesium carbonate; trifluoroacetic acid; In ethanol; acetic acid; N,N-dimethyl-formamide;

Reference yield:

: 1012880-03-3
2-(4-fluoro-2-methyl-5-nitrophenyl)acetic acid

: 1442470-60-1
7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-4-fluoro-2-methylphenyl)-1-isopropyl-1,6-naphthyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: sulfuric acid / 2.5 h / 85 °C

2: palladium 10% on activated carbon; hydrogen / ethanol / 2 h / 2660.18 Torr

3: caesium carbonate / N,N-dimethyl-formamide / 100 °C

4: trifluoroacetic acid / acetic acid / 8 h / 180 °C / Inert atmosphere

With sulfuric acid; palladium 10% on activated carbon; hydrogen; caesium carbonate; trifluoroacetic acid; In ethanol; acetic acid; N,N-dimethyl-formamide;