tert-butyl 1-(2-(4-chlorophenyl)-1-hydroxybutan-2-yl)-1H-indol-4-ylcarbamate

Base Information

Chemical Name:tert-butyl 1-(2-(4-chlorophenyl)-1-hydroxybutan-2-yl)-1H-indol-4-ylcarbamate
CAS No.:1389326-57-1
Molecular Formula:C₂₃H₂₇ClN₂O₃
Molecular Weight:414.932
Hs Code.:

Synonyms:tert-butyl 1-(2-(4-chlorophenyl)-1-hydroxybutan-2-yl)-1H-indol-4-ylcarbamate

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Chemical Property of tert-butyl 1-(2-(4-chlorophenyl)-1-hydroxybutan-2-yl)-1H-indol-4-ylcarbamate

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Technology Process of tert-butyl 1-(2-(4-chlorophenyl)-1-hydroxybutan-2-yl)-1H-indol-4-ylcarbamate

There total 6 articles about tert-butyl 1-(2-(4-chlorophenyl)-1-hydroxybutan-2-yl)-1H-indol-4-ylcarbamate 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:

: 1389326-22-0
methyl 2-{4-[(tert-butoxycarbonyl)amino]-1H-indol-1-yl}-2-(4-chlorophenyl)butanoate

: 1389326-57-1
tert-butyl 1-(2-(4-chlorophenyl)-1-hydroxybutan-2-yl)-1H-indol-4-ylcarbamate

Guidance literature:: methyl 2-{4-[(tert-butoxycarbonyl)amino]-1H-indol-1-yl}-2-(4-chlorophenyl)butanoate; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 4h;

With water; In tetrahydrofuran;

Reference yield:

: 24091-92-7
methyl 2-bromo-2-(4-chlorophenyl)acetate

: 1389326-57-1
tert-butyl 1-(2-(4-chlorophenyl)-1-hydroxybutan-2-yl)-1H-indol-4-ylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / 0 °C

1.2: 3 h / 0 °C

2.1: hydrogen / 10% Pt/activated carbon / ethyl acetate / 3 h / Inert atmosphere

3.1: sodium hydrogencarbonate / 1,4-dioxane; water

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.25 h / 0 °C

4.2: 2 h / 0 °C

5.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 0 - 20 °C

With lithium aluminium tetrahydride; hydrogen; sodium hydride; sodium hydrogencarbonate; 10% Pt/activated carbon; In tetrahydrofuran; 1,4-dioxane; water; ethyl acetate; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 4769-97-5
4-nitro-1H-indoIe

: 1389326-57-1
tert-butyl 1-(2-(4-chlorophenyl)-1-hydroxybutan-2-yl)-1H-indol-4-ylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / 0 °C

1.2: 3 h / 0 °C

2.1: hydrogen / 10% Pt/activated carbon / ethyl acetate / 3 h / Inert atmosphere

3.1: sodium hydrogencarbonate / 1,4-dioxane; water

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.25 h / 0 °C

4.2: 2 h / 0 °C

5.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / 0 - 20 °C

With lithium aluminium tetrahydride; hydrogen; sodium hydride; sodium hydrogencarbonate; 10% Pt/activated carbon; In tetrahydrofuran; 1,4-dioxane; water; ethyl acetate; N,N-dimethyl-formamide; mineral oil;