ethyl 3-[3-(ethoxycarbonyl)benzyl]-1-[(6-ethylbenzo[d][1,3]dioxol-5-yl)methyl]-6-hydroxy-4-oxo-1,4-dihydroquinoline-2-carboxylate

Base Information

Chemical Name:ethyl 3-[3-(ethoxycarbonyl)benzyl]-1-[(6-ethylbenzo[d][1,3]dioxol-5-yl)methyl]-6-hydroxy-4-oxo-1,4-dihydroquinoline-2-carboxylate
CAS No.:1159608-54-4
Molecular Formula:C₃₂H₃₁NO₈
Molecular Weight:557.6
Hs Code.:

Synonyms:ethyl 3-[3-(ethoxycarbonyl)benzyl]-1-[(6-ethylbenzo[d][1,3]dioxol-5-yl)methyl]-6-hydroxy-4-oxo-1,4-dihydroquinoline-2-carboxylate

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Chemical Property of ethyl 3-[3-(ethoxycarbonyl)benzyl]-1-[(6-ethylbenzo[d][1,3]dioxol-5-yl)methyl]-6-hydroxy-4-oxo-1,4-dihydroquinoline-2-carboxylate

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Technology Process of ethyl 3-[3-(ethoxycarbonyl)benzyl]-1-[(6-ethylbenzo[d][1,3]dioxol-5-yl)methyl]-6-hydroxy-4-oxo-1,4-dihydroquinoline-2-carboxylate

There total 10 articles about ethyl 3-[3-(ethoxycarbonyl)benzyl]-1-[(6-ethylbenzo[d][1,3]dioxol-5-yl)methyl]-6-hydroxy-4-oxo-1,4-dihydroquinoline-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: 90.0%

: ethyl-3-(3-(ethoxycarbonyl)benzyl)-1-((6-ethylbenzo[d][1,3]dioxol-5-yl)methyl)-4-oxo-6-((2,3,3-trimethylbutan-2-yl)oxy)-1,4-dihydroquinoline-2-carboxylate

: 1159608-54-4
ethyl 3-[3-(ethoxycarbonyl)benzyl]-1-[(6-ethylbenzo[d][1,3]dioxol-5-yl)methyl]-6-hydroxy-4-oxo-1,4-dihydroquinoline-2-carboxylate

Guidance literature:: With hydrogenchloride; In ethanol; at 0 - 20 ℃; for 12h;
DOI:10.1016/j.bmcl.2017.04.049

Reference yield:

(E)-3-(3-(5-hydroxy-2-nitrophenyl)-3-oxoprop-1-en-1-yl)benzoic acid: 1159608-45-3
(E)-3-(3-(5-hydroxy-2-nitrophenyl)-3-oxoprop-1-en-1-yl)benzoic acid

: 1159608-54-4
ethyl 3-[3-(ethoxycarbonyl)benzyl]-1-[(6-ethylbenzo[d][1,3]dioxol-5-yl)methyl]-6-hydroxy-4-oxo-1,4-dihydroquinoline-2-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydrogenchloride / ethanol / 12 h / 0 °C

2.1: 1H-imidazole / N,N-dimethyl-formamide / 48 h / 20 °C

3.1: platinum(IV) oxide / ethanol / 2 h / 20 °C / 3620.13 Torr

4.1: 1,2-dichloro-ethane / 0.25 h / 20 °C

4.2: 5 h / 20 °C

5.1: triethylamine / N,N-dimethyl-formamide / 0.25 h / 0 - 20 °C

5.2: 4 h / 20 °C

6.1: ethanol / 2 h / 20 °C

7.1: hydrogenchloride / ethanol / 12 h / 0 - 20 °C

With 1H-imidazole; hydrogenchloride; platinum(IV) oxide; triethylamine; In ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2017.04.049

Reference yield:

: 75889-41-7
6-ethylbenzo[d][1,3]dioxole-5-carbaldehyde

: 1159608-54-4
ethyl 3-[3-(ethoxycarbonyl)benzyl]-1-[(6-ethylbenzo[d][1,3]dioxol-5-yl)methyl]-6-hydroxy-4-oxo-1,4-dihydroquinoline-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1,2-dichloro-ethane / 0.25 h / 20 °C

1.2: 5 h / 20 °C

2.1: triethylamine / N,N-dimethyl-formamide / 0.25 h / 0 - 20 °C

2.2: 4 h / 20 °C

3.1: ethanol / 2 h / 20 °C

4.1: hydrogenchloride / ethanol / 12 h / 0 - 20 °C

With hydrogenchloride; triethylamine; In ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2017.04.049