3-[2'-(S)-(1'''-naphthylacetyl)amino-3'-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone

Base Information

Chemical Name:3-[2'-(S)-(1'''-naphthylacetyl)amino-3'-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone
CAS No.:356578-38-6
Molecular Formula:C₃₈H₃₇N₃O₆
Molecular Weight:631.728
Hs Code.:

Synonyms:3-[2'-(S)-(1'''-naphthylacetyl)amino-3'-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone

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Chemical Property of 3-[2'-(S)-(1'''-naphthylacetyl)amino-3'-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone

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Technology Process of 3-[2'-(S)-(1'''-naphthylacetyl)amino-3'-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone

There total 7 articles about 3-[2'-(S)-(1'''-naphthylacetyl)amino-3'-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone 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: 86.0%

: 86-87-3
naphth-1-yl acetic acid

: 356578-36-4
3-[2'-(S)-amino-3-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone

: 356578-38-6
3-[2'-(S)-(1'''-naphthylacetyl)amino-3'-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone

Guidance literature:: naphth-1-yl acetic acid; With N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; at 0 ℃; for 0.333333h;

3-[2'-(S)-amino-3-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone; With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃; Further stages.;
DOI:10.1021/jm000446q

Reference yield:

: 21901-18-8
4-Methyl-3-nitro-2-pyridone

: 356578-38-6
3-[2'-(S)-(1'''-naphthylacetyl)amino-3'-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaH / dimethylformamide / 1 h

1.2: 56 percent / dimethylformamide / 20 °C

2.1: 96 percent / H₂ / 10percent Pd/C / ethanol / 5.5 h / 2068.65 Torr

3.1: EDC / CH₂Cl₂ / 0.33 h / 0 °C

3.2: 27 percent / CH₂Cl₂ / 0 - 20 °C

4.1: TFA / CH₂Cl₂ / 20 °C

5.1: EDC / CH₂Cl₂ / 0.33 h / 0 °C

5.2: 86 percent / iPr₂NEt / CH₂Cl₂ / 0 - 20 °C

With hydrogen; sodium hydride; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; trifluoroacetic acid; 10percent Pd/C; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm000446q

Reference yield:

: 824-94-2
p-methoxybenzyl chloride

: 356578-38-6
3-[2'-(S)-(1'''-naphthylacetyl)amino-3'-(4''-methoxycarbonylmethyl)benzene]propanoylamino-1-(4-methoxybenzyl)-4-methyl-2-pyridone

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaH / dimethylformamide / 1 h

1.2: 56 percent / dimethylformamide / 20 °C

2.1: 96 percent / H₂ / 10percent Pd/C / ethanol / 5.5 h / 2068.65 Torr

3.1: EDC / CH₂Cl₂ / 0.33 h / 0 °C

3.2: 27 percent / CH₂Cl₂ / 0 - 20 °C

4.1: TFA / CH₂Cl₂ / 20 °C

5.1: EDC / CH₂Cl₂ / 0.33 h / 0 °C

5.2: 86 percent / iPr₂NEt / CH₂Cl₂ / 0 - 20 °C

With hydrogen; sodium hydride; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; trifluoroacetic acid; 10percent Pd/C; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm000446q