7-hydroxy-2-methyl-6-(3-oxo-3-phenyl-propyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzoimidazole-5-carboxylic acid dimethylamide

Base Information

Chemical Name:7-hydroxy-2-methyl-6-(3-oxo-3-phenyl-propyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzoimidazole-5-carboxylic acid dimethylamide
CAS No.:774582-77-3
Molecular Formula:C₂₆H₃₅N₃O₄Si
Molecular Weight:481.667
Hs Code.:

Synonyms:7-hydroxy-2-methyl-6-(3-oxo-3-phenyl-propyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzoimidazole-5-carboxylic acid dimethylamide

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Chemical Property of 7-hydroxy-2-methyl-6-(3-oxo-3-phenyl-propyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzoimidazole-5-carboxylic acid dimethylamide

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Technology Process of 7-hydroxy-2-methyl-6-(3-oxo-3-phenyl-propyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzoimidazole-5-carboxylic acid dimethylamide

There total 6 articles about 7-hydroxy-2-methyl-6-(3-oxo-3-phenyl-propyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzoimidazole-5-carboxylic acid dimethylamide 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: 73.0%

: 774582-78-4
4-hydroxy-N,N,2-trimethyl-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazole-6-carboxamide

: 3433-56-5
1-(1-phenylvinyl)pyrrolidine

: 33797-51-2
eschenmoser's salt

: 774582-77-3
7-hydroxy-2-methyl-6-(3-oxo-3-phenyl-propyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzoimidazole-5-carboxylic acid dimethylamide

Guidance literature:: 4-hydroxy-N,N,2-trimethyl-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazole-6-carboxamide; eschenmoser's salt; In dichloromethane; at 20 ℃; for 3h;

1-(1-phenylvinyl)pyrrolidine; In toluene; for 3h; Heating / reflux;

With sodium hydroxide; (2E)-but-2-enedioic acid; more than 3 stages;

Reference yield:

: 774582-78-4
4-hydroxy-N,N,2-trimethyl-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazole-6-carboxamide

: N,N-dimethyleneammonium iodide

: 774582-77-3
7-hydroxy-2-methyl-6-(3-oxo-3-phenyl-propyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzoimidazole-5-carboxylic acid dimethylamide

Guidance literature:: 4-hydroxy-N,N,2-trimethyl-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazole-6-carboxamide; N,N-dimethyleneammonium iodide; In dichloromethane; at 20 ℃; for 3h;

In toluene; for 3h; Heating / reflux;

With sodium hydroxide; (2E)-but-2-enedioic acid; more than 3 stages;

Reference yield:

: 4-(benzyloxy)-N,N,2-trimethyl-1-{[2-(trimethylsilyl)ethoxy]-methyl}-1H-benzimidazole-6-carboxamide

: 774582-77-3
7-hydroxy-2-methyl-6-(3-oxo-3-phenyl-propyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-benzoimidazole-5-carboxylic acid dimethylamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen / palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 3750.38 Torr

2.1: dichloromethane / 3 h / 20 °C

2.2: 3 h / Heating / reflux

With hydrogen; palladium 10% on activated carbon; In ethanol; dichloromethane;