ethyl 7-[(4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzyl)oxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate

Base Information

Chemical Name:ethyl 7-[(4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzyl)oxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate
CAS No.:949495-44-7
Molecular Formula:C₂₄H₂₃NO₁₀
Molecular Weight:485.447
Hs Code.:

Synonyms:ethyl 7-[(4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzyl)oxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate

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Chemical Property of ethyl 7-[(4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzyl)oxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate

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Technology Process of ethyl 7-[(4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzyl)oxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate

There total 5 articles about ethyl 7-[(4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzyl)oxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate 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: 57.0%

: 949495-43-6
ethyl {[4-(hydroxymethyl)-2-methoxyphenyl]amino}(oxo)acetate

: 949495-41-4
ethyl 5,7-dihydroxy-4-oxo-4H-chromene-2-carboxylate

: 949495-44-7
ethyl 7-[(4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzyl)oxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃;
DOI:10.1021/jm070336k

Reference yield:

: 949495-42-5
4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzoic acid

: 949495-44-7
ethyl 7-[(4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzyl)oxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 69 percent / trimethyl borate; BH₃*THF / tetrahydrofuran / 6 h / 20 °C

2: 57 percent / DIAD; triphenylphosphine / tetrahydrofuran / 20 °C

With borane-THF; Trimethyl borate; di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; 2: Mitsunobu reaction;
DOI:10.1021/jm070336k

Reference yield:

: 480-66-0,67471-34-5
2,4,6-trihydroxyacetophenone

: 949495-44-7
ethyl 7-[(4-{[ethoxy(oxo)acetyl]amino}-3-methoxybenzyl)oxy]-5-hydroxy-4-oxo-4H-chromene-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine / 20 °C

1.2: aq. Na₂CO₃ / ethanol / 2 h / 60 - 70 °C

2.1: 180 mg / sulfuric acid / Heating

3.1: 57 percent / DIAD; triphenylphosphine / tetrahydrofuran / 20 °C

With pyridine; di-isopropyl azodicarboxylate; sulfuric acid; triphenylphosphine; In tetrahydrofuran; 3.1: Mitsunobu reaction;
DOI:10.1021/jm070336k