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

Base Information

Chemical Name:N-(2-(3-benzyl-2-(methylamino)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide
CAS No.:1359935-94-6
Molecular Formula:C₂₃H₂₈N₄O₃S
Molecular Weight:440.566
Hs Code.:

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

There total 5 articles about N-(2-(3-benzyl-2-(methylamino)-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:

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

: 1359935-94-6
N-(2-(3-benzyl-2-(methylamino)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Guidance literature:: ethyl 1-benzyl-6-(2-(1-methyl-1H-imidazole-4-sulfonamido)ethoxy)-2,3-dihydro-1H-inden-2-ylcarbamate; With lithium aluminium tetrahydride; In tetrahydrofuran; for 2h; Reflux;

With sodium hydroxide; at 20 ℃;

Reference yield:

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

: 1359935-94-6
N-(2-(3-benzyl-2-(methylamino)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Guidance literature:: Multi-step reaction with 4 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: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / Reflux

4.2: 20 °C

With dmap; lithium aluminium tetrahydride; formic acid; caesium carbonate; In tetrahydrofuran; dichloromethane; acetonitrile;

Reference yield:

: 1359937-94-2
ethyl 6-(2-aminoethoxy)-1-benzyl-2,3-dihydro-1H-inden-2-ylcarbamate

: 1359935-94-6
N-(2-(3-benzyl-2-(methylamino)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: dmap / dichloromethane / 20 °C

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / Reflux

2.2: 20 °C

With dmap; lithium aluminium tetrahydride; In tetrahydrofuran; dichloromethane;