N-(2-{[3-Benzyl-2-(3,3-dimethylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yl]oxy}ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Base Information

Chemical Name:N-(2-{[3-Benzyl-2-(3,3-dimethylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yl]oxy}ethyl)-1-methyl-1H-imidazole-4-sulfonamide
CAS No.:1359938-04-7
Molecular Formula:C₂₇H₃₄N₄O₃S
Molecular Weight:494.658
Hs Code.:

Synonyms:N-(2-{[3-Benzyl-2-(3,3-dimethylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yl]oxy}ethyl)-1-methyl-1H-imidazole-4-sulfonamide

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Chemical Property of N-(2-{[3-Benzyl-2-(3,3-dimethylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yl]oxy}ethyl)-1-methyl-1H-imidazole-4-sulfonamide

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Technology Process of N-(2-{[3-Benzyl-2-(3,3-dimethylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yl]oxy}ethyl)-1-methyl-1H-imidazole-4-sulfonamide

There total 8 articles about N-(2-{[3-Benzyl-2-(3,3-dimethylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yl]oxy}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:

: 1359938-06-9
N-(2-(3-benzyl-2-(3-chloro-2,2-dimethylpropylamino)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

: 1359938-04-7
N-(2-{[3-Benzyl-2-(3,3-dimethylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yl]oxy}ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Guidance literature:: With sodium hydrogencarbonate; In acetonitrile; at 70 ℃; for 2h; Microwave irradiation;

Reference yield:

: cis-ethyl 1-benzyl-6-methoxy-2,3-dihydro-1H-inden-2-ylcarbamate

: 1359938-04-7
N-(2-{[3-Benzyl-2-(3,3-dimethylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yl]oxy}ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Guidance literature:: Multi-step reaction with 8 steps

1.1: boron tribromide / dichloromethane / Inert atmosphere

1.2: Cooling with ice

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

2.2: 2 h / 50 - 80 °C

3.1: formic acid / 20 °C

4.1: dmap / dichloromethane / 20 °C

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

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

7.1: borane dimethyl complex / tetrahydrofuran / 20 - 60 °C

7.2: 2 h / Reflux

8.1: sodium hydrogencarbonate / acetonitrile / 2 h / 70 °C / Microwave irradiation

With dmap; formic acid; boron tribromide; sodium hydrogencarbonate; caesium carbonate; diisopropylamine; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; acetonitrile;

Reference yield:

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

: 1359938-04-7
N-(2-{[3-Benzyl-2-(3,3-dimethylazetidin-1-yl)-2,3-dihydro-1H-inden-5-yl]oxy}ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: diisopropylamine / dichloromethane / 20 °C / Inert atmosphere

2.1: borane dimethyl complex / tetrahydrofuran / 20 - 60 °C

2.2: 2 h / Reflux

3.1: sodium hydrogencarbonate / acetonitrile / 2 h / 70 °C / Microwave irradiation

With sodium hydrogencarbonate; diisopropylamine; In tetrahydrofuran; dichloromethane; acetonitrile;