[2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazol-4-yl]methanol

Base Information

Chemical Name:[2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazol-4-yl]methanol
CAS No.:1372540-40-3
Molecular Formula:C₂₂H₂₄F₃N₃O₂
Molecular Weight:419.447
Hs Code.:

Synonyms:[2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazol-4-yl]methanol

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Chemical Property of [2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazol-4-yl]methanol

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Technology Process of [2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazol-4-yl]methanol

There total 5 articles about [2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazol-4-yl]methanol 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: 88.0%

: 1372540-24-3
methyl 2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylate

: 1372540-40-3
[2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazol-4-yl]methanol

Guidance literature:: methyl 2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylate; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 0.5h;

With water; sodium hydroxide; In tetrahydrofuran;

Reference yield:

: 2516-95-2
5-chloro-2-nitrobenzoic acid

: 1372540-40-3
[2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazol-4-yl]methanol

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium tert-butylate; N-methoxylamine hydrochloride / copper diacetate / N,N-dimethyl-formamide / 3 h / 0 °C / Inert atmosphere

1.2: pH 1

2.1: triethylamine; HATU / tetrahydrofuran / 3 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 110 °C

4.1: iron / 5 h / Reflux

5.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 80 °C

6.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / 0 °C

With lithium aluminium tetrahydride; potassium tert-butylate; N-methoxylamine hydrochloride; iron; potassium carbonate; triethylamine; HATU; copper diacetate; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 874301-23-2
3-amino-5-chloro-2-nitrobenzoic acid methyl ester

: 1372540-40-3
[2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazol-4-yl]methanol

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 110 °C

2: iron / 5 h / Reflux

3: potassium carbonate / N,N-dimethyl-formamide / 3 h / 80 °C

4: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / 0 °C

With lithium aluminium tetrahydride; iron; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide;