methyl 2-(4-chlorophenyl)-4-fluoro-2-(4-(methylsulfonamido)-1H-indol-1-yl)butanoate

Base Information

Chemical Name:methyl 2-(4-chlorophenyl)-4-fluoro-2-(4-(methylsulfonamido)-1H-indol-1-yl)butanoate
CAS No.:1389325-77-2
Molecular Formula:C₂₀H₂₀ClFN₂O₄S
Molecular Weight:438.907
Hs Code.:

Synonyms:methyl 2-(4-chlorophenyl)-4-fluoro-2-(4-(methylsulfonamido)-1H-indol-1-yl)butanoate

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Chemical Property of methyl 2-(4-chlorophenyl)-4-fluoro-2-(4-(methylsulfonamido)-1H-indol-1-yl)butanoate

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Technology Process of methyl 2-(4-chlorophenyl)-4-fluoro-2-(4-(methylsulfonamido)-1H-indol-1-yl)butanoate

There total 6 articles about methyl 2-(4-chlorophenyl)-4-fluoro-2-(4-(methylsulfonamido)-1H-indol-1-yl)butanoate 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:

: 1389326-75-3
methyl 2-(4-amino-1H-indol-1-yl)-2-(4-chlorophenyl)-4-fluorobutanoate

: 124-63-0
methanesulfonyl chloride

: 1389325-77-2
methyl 2-(4-chlorophenyl)-4-fluoro-2-(4-(methylsulfonamido)-1H-indol-1-yl)butanoate

Guidance literature:: With 4-methyl-morpholine; In dichloromethane; at 20 ℃; for 4h;

Reference yield:

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

: 1389325-77-2
methyl 2-(4-chlorophenyl)-4-fluoro-2-(4-(methylsulfonamido)-1H-indol-1-yl)butanoate

Guidance literature:: Multi-step reaction with 6 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 / 1 h / 0 °C / Inert atmosphere

4.2: 4 h / 20 °C

5.1: hydrogenchloride / methanol / 2 h / 20 °C

6.1: 4-methyl-morpholine / dichloromethane / 4 h / 20 °C

With 4-methyl-morpholine; hydrogenchloride; hydrogen; sodium hydride; sodium hydrogencarbonate; 10% Pt/activated carbon; In 1,4-dioxane; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; mineral oil;

Reference yield:

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

: 1389325-77-2
methyl 2-(4-chlorophenyl)-4-fluoro-2-(4-(methylsulfonamido)-1H-indol-1-yl)butanoate

Guidance literature:: Multi-step reaction with 6 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 / 1 h / 0 °C / Inert atmosphere

4.2: 4 h / 20 °C

5.1: hydrogenchloride / methanol / 2 h / 20 °C

6.1: 4-methyl-morpholine / dichloromethane / 4 h / 20 °C

With 4-methyl-morpholine; hydrogenchloride; hydrogen; sodium hydride; sodium hydrogencarbonate; 10% Pt/activated carbon; In 1,4-dioxane; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; mineral oil;