1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(2-amino-1-benzylethyl)-4-fluorophenoxy]ethyl}amide

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Chemical Name:1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(2-amino-1-benzylethyl)-4-fluorophenoxy]ethyl}amide
CAS No.:1359840-78-0
Molecular Formula:C₂₁H₂₅FN₄O₃S
Molecular Weight:432.519
Hs Code.:

Synonyms:1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(2-amino-1-benzylethyl)-4-fluorophenoxy]ethyl}amide

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Chemical Property of 1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(2-amino-1-benzylethyl)-4-fluorophenoxy]ethyl}amide

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Technology Process of 1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(2-amino-1-benzylethyl)-4-fluorophenoxy]ethyl}amide

There total 8 articles about 1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(2-amino-1-benzylethyl)-4-fluorophenoxy]ethyl}amide 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: 36.0%

: 1359840-77-9
1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(benzylcyanomethyl)-4-fluorophenoxy]ethyl}amide

: 1359840-78-0
1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(2-amino-1-benzylethyl)-4-fluorophenoxy]ethyl}amide

Guidance literature:: 1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(benzylcyanomethyl)-4-fluorophenoxy]ethyl}amide; With diisobutylaluminium hydride; In dichloromethane; toluene; at 0 ℃; for 0.5h;

With sodium tetrahydroborate; In tetrahydrofuran; methanol; dichloromethane; toluene; at 0 - 20 ℃; for 1h;

Reference yield:

: 100-52-7
benzaldehyde

: 1359840-78-0
1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(2-amino-1-benzylethyl)-4-fluorophenoxy]ethyl}amide

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium ethanolate / ethanol / 20 °C

2.1: sodium tetrahydroborate / ethanol / 20 °C

3.1: boron tribromide / dichloromethane / 0 - 20 °C / Inert atmosphere

4.1: caesium carbonate / acetonitrile / 1 h / 80 °C / Inert atmosphere

4.2: 2 h / 50 - 80 °C

5.1: hydrogenchloride / 1,4-dioxane / 20 °C

6.1: dmap / dichloromethane / 20 °C / Inert atmosphere

7.1: diisobutylaluminium hydride / dichloromethane; toluene / 0.5 h / 0 °C

7.2: 1 h / 0 - 20 °C

With hydrogenchloride; dmap; sodium tetrahydroborate; sodium ethanolate; boron tribromide; diisobutylaluminium hydride; caesium carbonate; In 1,4-dioxane; ethanol; dichloromethane; toluene; acetonitrile;

Reference yield:

: 1359840-72-4
2-(2-fluoro-5-methoxyphenyl)-3-phenylacrylonitrile

: 1359840-78-0
1-methyl-1H-imidazole-4-sulfonic acid {2-[3-(2-amino-1-benzylethyl)-4-fluorophenoxy]ethyl}amide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium tetrahydroborate / ethanol / 20 °C

2.1: boron tribromide / dichloromethane / 0 - 20 °C / Inert atmosphere

3.1: caesium carbonate / acetonitrile / 1 h / 80 °C / Inert atmosphere

3.2: 2 h / 50 - 80 °C

4.1: hydrogenchloride / 1,4-dioxane / 20 °C

5.1: dmap / dichloromethane / 20 °C / Inert atmosphere

6.1: diisobutylaluminium hydride / dichloromethane; toluene / 0.5 h / 0 °C

6.2: 1 h / 0 - 20 °C

With hydrogenchloride; dmap; sodium tetrahydroborate; boron tribromide; diisobutylaluminium hydride; caesium carbonate; In 1,4-dioxane; ethanol; dichloromethane; toluene; acetonitrile;