(S)-N-(4-(4-methoxyphenethylamino)-3,4-dioxo-1-phenylbutan-2-yl)-6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxamide

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Chemical Name:(S)-N-(4-(4-methoxyphenethylamino)-3,4-dioxo-1-phenylbutan-2-yl)-6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxamide
CAS No.:1298120-33-8
Molecular Formula:C₃₁H₃₀N₂O₈
Molecular Weight:558.588
Hs Code.:

Synonyms:(S)-N-(4-(4-methoxyphenethylamino)-3,4-dioxo-1-phenylbutan-2-yl)-6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxamide

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Chemical Property of (S)-N-(4-(4-methoxyphenethylamino)-3,4-dioxo-1-phenylbutan-2-yl)-6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxamide

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Technology Process of (S)-N-(4-(4-methoxyphenethylamino)-3,4-dioxo-1-phenylbutan-2-yl)-6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxamide

There total 7 articles about (S)-N-(4-(4-methoxyphenethylamino)-3,4-dioxo-1-phenylbutan-2-yl)-6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxamide 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: 44.0%

: C₃₃H₃₄N₂O₉

: 1298120-33-8
(S)-N-(4-(4-methoxyphenethylamino)-3,4-dioxo-1-phenylbutan-2-yl)-6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxamide

Guidance literature:: With hydrogenchloride; In methanol; at 70 ℃; for 2h;
DOI:10.1016/j.ejmech.2011.02.025

Reference yield:

: 1298119-95-5
C₁₆H₁₈O₇

: 1298120-33-8
(S)-N-(4-(4-methoxyphenethylamino)-3,4-dioxo-1-phenylbutan-2-yl)-6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium hydroxide / ethanol; water / 1 h / 20 °C

1.2: pH 2

2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 2 h / 0 - 20 °C

3.1: Dess-Martin periodane / N,N-dimethyl-formamide / 2 h / 0 - 20 °C

4.1: hydrogenchloride / methanol / 2 h / 70 °C

With hydrogenchloride; benzotriazol-1-ol; Dess-Martin periodane; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; potassium hydroxide; In methanol; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2011.02.025

Reference yield:

: 1298119-90-0
ethyl 6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxylate

: 1298120-33-8
(S)-N-(4-(4-methoxyphenethylamino)-3,4-dioxo-1-phenylbutan-2-yl)-6-hydroxy-7-methoxy-3-methyl-4-oxo-4H-chromene-2-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 - 20 °C

2.1: potassium hydroxide / ethanol; water / 1 h / 20 °C

2.2: pH 2

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 2 h / 0 - 20 °C

4.1: Dess-Martin periodane / N,N-dimethyl-formamide / 2 h / 0 - 20 °C

5.1: hydrogenchloride / methanol / 2 h / 70 °C

With hydrogenchloride; benzotriazol-1-ol; Dess-Martin periodane; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2011.02.025