N-(2-(3-benzyl-2-(3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Base Information

Chemical Name:N-(2-(3-benzyl-2-(3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide
CAS No.:1359938-03-6
Molecular Formula:C₂₆H₃₂N₄O₃S
Molecular Weight:480.631
Hs Code.:

Synonyms:N-(2-(3-benzyl-2-(3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

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Chemical Property of N-(2-(3-benzyl-2-(3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

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Technology Process of N-(2-(3-benzyl-2-(3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

There total 6 articles about N-(2-(3-benzyl-2-(3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide 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: 10.0%

: 6974-77-2
1-bromo-3-chloro-2-methyl propane

: 1359938-01-4
N-(2-(2-amino-3-benzyl-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

: 1359938-03-6
N-(2-(3-benzyl-2-(3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Guidance literature:: With potassium carbonate; In water; acetonitrile; at 120 ℃; for 0.666667h;

Reference yield:

: 1359937-93-1
ethyl 1-benzyl-6-(2-(1-methyl-1H-imidazole-4-sulfonamido)ethoxy)-2,3-dihydro-1H-inden-2-ylcarbamate

: 1359938-03-6
N-(2-(3-benzyl-2-(3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / ethanol / 1 h / 100 °C / Microwave irradiation

2: potassium carbonate / acetonitrile; water / 0.67 h / 120 °C

With potassium carbonate; potassium hydroxide; In ethanol; water; acetonitrile;

Reference yield:

: ethyl 1-benzyl-6-hydroxy-2,3-dihydro-1H-indene-2-ylcarbamate

: 1359938-03-6
N-(2-(3-benzyl-2-(3-methylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Guidance literature:: Multi-step reaction with 5 steps

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

1.2: 2 h / 50 - 80 °C

2.1: formic acid / 20 °C

3.1: dmap / dichloromethane / 20 °C

4.1: potassium hydroxide / ethanol / 1 h / 100 °C / Microwave irradiation

5.1: potassium carbonate / acetonitrile; water / 0.67 h / 120 °C

With dmap; formic acid; potassium carbonate; caesium carbonate; potassium hydroxide; In ethanol; dichloromethane; water; acetonitrile;