(R)-(3-Acetylamino-5-benzylcarbamoyl-6-methyl-2-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl-acetic acid ethyl ester

Base Information

Chemical Name:(R)-(3-Acetylamino-5-benzylcarbamoyl-6-methyl-2-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl-acetic acid ethyl ester
CAS No.:185856-28-4
Molecular Formula:C₂₆H₂₉N₃O₅
Molecular Weight:463.533
Hs Code.:

Synonyms:(R)-(3-Acetylamino-5-benzylcarbamoyl-6-methyl-2-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl-acetic acid ethyl ester

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Chemical Property of (R)-(3-Acetylamino-5-benzylcarbamoyl-6-methyl-2-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl-acetic acid ethyl ester

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Technology Process of (R)-(3-Acetylamino-5-benzylcarbamoyl-6-methyl-2-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl-acetic acid ethyl ester

There total 3 articles about (R)-(3-Acetylamino-5-benzylcarbamoyl-6-methyl-2-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl-acetic acid ethyl ester 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:

: 882-36-0
N-benzyl-3-oxobutanamide

: 185856-28-4
(R)-(3-Acetylamino-5-benzylcarbamoyl-6-methyl-2-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: BF₃*OEt₂ / benzene / Heating

2: EtO₂CCl / tetrahydrofuran / 14 h / Ambient temperature

With boron trifluoride diethyl etherate; chloroformic acid ethyl ester; In tetrahydrofuran; benzene;
DOI:10.1021/jo9600520

Reference yield:

: 100-46-9
benzylamine

: 185856-28-4
(R)-(3-Acetylamino-5-benzylcarbamoyl-6-methyl-2-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / NaHCO₃ / benzene / 14 h / Ambient temperature

2: BF₃*OEt₂ / benzene / Heating

3: EtO₂CCl / tetrahydrofuran / 14 h / Ambient temperature

With boron trifluoride diethyl etherate; chloroformic acid ethyl ester; sodium hydrogencarbonate; In tetrahydrofuran; benzene;
DOI:10.1021/jo9600520

Reference yield:

: Sodium; 2-acetylamino-acrylate

: 1027948-17-9
(R)-((Z)-2-Benzylcarbamoyl-1-methyl-vinylamino)-phenyl-acetic acid ethyl ester

: 185856-28-4
(R)-(3-Acetylamino-5-benzylcarbamoyl-6-methyl-2-oxo-3,4-dihydro-2H-pyridin-1-yl)-phenyl-acetic acid ethyl ester

Guidance literature:: With chloroformic acid ethyl ester; In tetrahydrofuran; for 14h; Yield given; Ambient temperature;
DOI:10.1021/jo9600520