N-[4-(1-benzenesulfonyl-1H-indol-2-yl)but-1-enyl]-N-benzyl-2-ethylsulfenylacetamide

Base Information

Chemical Name:N-[4-(1-benzenesulfonyl-1H-indol-2-yl)but-1-enyl]-N-benzyl-2-ethylsulfenylacetamide
CAS No.:459832-04-3
Molecular Formula:C₂₉H₃₀N₂O₃S₂
Molecular Weight:518.701
Hs Code.:

Synonyms:N-[4-(1-benzenesulfonyl-1H-indol-2-yl)but-1-enyl]-N-benzyl-2-ethylsulfenylacetamide

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Chemical Property of N-[4-(1-benzenesulfonyl-1H-indol-2-yl)but-1-enyl]-N-benzyl-2-ethylsulfenylacetamide

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Technology Process of N-[4-(1-benzenesulfonyl-1H-indol-2-yl)but-1-enyl]-N-benzyl-2-ethylsulfenylacetamide

There total 2 articles about N-[4-(1-benzenesulfonyl-1H-indol-2-yl)but-1-enyl]-N-benzyl-2-ethylsulfenylacetamide 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:

: 165532-83-2
1-Benzenesulfonyl-2-(4-bromobutanyl)-1H-indole

: 459832-04-3
N-[4-(1-benzenesulfonyl-1H-indol-2-yl)but-1-enyl]-N-benzyl-2-ethylsulfenylacetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 69 percent / silver(I) tetrafluoroborate; DMSO / 18 h / 20 °C

2: magnesium sulfate / CH₂Cl₂ / 2 h / 20 °C

3: 0.9 g / pyridine / CH₂Cl₂ / 3 h / 20 °C

With pyridine; silver tetrafluoroborate; magnesium sulfate; dimethyl sulfoxide; In dichloromethane;
DOI:10.1021/jo020083x

Reference yield:

: 459832-03-2
4-(1-benzenesulfonyl-1H-indol-2-yl)butyraldehyde

: 459832-04-3
N-[4-(1-benzenesulfonyl-1H-indol-2-yl)but-1-enyl]-N-benzyl-2-ethylsulfenylacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: magnesium sulfate / CH₂Cl₂ / 2 h / 20 °C

2: 0.9 g / pyridine / CH₂Cl₂ / 3 h / 20 °C

With pyridine; magnesium sulfate; In dichloromethane;
DOI:10.1021/jo020083x