ethyl N-[1-(4-hydroxy-3-isopropylbenzyl)-2-methyl-1H-indol-4-yl]oxamate

Base Information

Chemical Name:ethyl N-[1-(4-hydroxy-3-isopropylbenzyl)-2-methyl-1H-indol-4-yl]oxamate
CAS No.:1000602-30-1
Molecular Formula:C₂₃H₂₆N₂O₄
Molecular Weight:394.47
Hs Code.:

Synonyms:ethyl N-[1-(4-hydroxy-3-isopropylbenzyl)-2-methyl-1H-indol-4-yl]oxamate

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Chemical Property of ethyl N-[1-(4-hydroxy-3-isopropylbenzyl)-2-methyl-1H-indol-4-yl]oxamate

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Technology Process of ethyl N-[1-(4-hydroxy-3-isopropylbenzyl)-2-methyl-1H-indol-4-yl]oxamate

There total 9 articles about ethyl N-[1-(4-hydroxy-3-isopropylbenzyl)-2-methyl-1H-indol-4-yl]oxamate 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: 23.0%

: 1000605-54-8
ethyl N-[1-(3-isopropyl-4-triisopropylsilanyloxybenzyl)-2-methyl-1H-indol-4-yl]oxamate

: 1000602-30-1
ethyl N-[1-(4-hydroxy-3-isopropylbenzyl)-2-methyl-1H-indol-4-yl]oxamate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.1016/j.bmc.2013.11.001

Reference yield:

: 26307-50-6
4-bromo-2-isopropyl-phenol

: 1000602-30-1
ethyl N-[1-(4-hydroxy-3-isopropylbenzyl)-2-methyl-1H-indol-4-yl]oxamate

Guidance literature:: Multi-step reaction with 7 steps

1.1: 1H-imidazole / N,N-dimethyl-formamide / 24 h / 20 °C

2.1: n-butyllithium / tetrahydrofuran; pentane / 2 h / -78 °C

2.2: 4 h / -78 - 20 °C

3.1: thionyl chloride / dichloromethane / 2 h / 20 °C

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 5 °C

4.2: 3 h / 5 °C

5.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; ethanol / 3 h / 20 °C

6.1: 3 h / 100 °C

7.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 20 °C

With 1H-imidazole; n-butyllithium; thionyl chloride; palladium 10% on activated carbon; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; mineral oil; pentane;
DOI:10.1016/j.bmc.2013.11.001

Reference yield:

: 88-69-7
2-(1-methylethyl)phenol

: 1000602-30-1
ethyl N-[1-(4-hydroxy-3-isopropylbenzyl)-2-methyl-1H-indol-4-yl]oxamate

Guidance literature:: Multi-step reaction with 8 steps

1.1: N-Bromosuccinimide / acetonitrile / 4 h / 0 - 20 °C

2.1: 1H-imidazole / N,N-dimethyl-formamide / 24 h / 20 °C

3.1: n-butyllithium / tetrahydrofuran; pentane / 2 h / -78 °C

3.2: 4 h / -78 - 20 °C

4.1: thionyl chloride / dichloromethane / 2 h / 20 °C

5.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 5 °C

5.2: 3 h / 5 °C

6.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; ethanol / 3 h / 20 °C

7.1: 3 h / 100 °C

8.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 20 °C

With 1H-imidazole; N-Bromosuccinimide; n-butyllithium; thionyl chloride; palladium 10% on activated carbon; tetrabutyl ammonium fluoride; hydrogen; sodium hydride; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile; mineral oil; pentane;
DOI:10.1016/j.bmc.2013.11.001