(R)-3-(N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)sulfamoyl)propyl acetate

Base Information

Chemical Name:(R)-3-(N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)sulfamoyl)propyl acetate
CAS No.:1380335-96-5
Molecular Formula:C₂₀H₃₁NO₆S
Molecular Weight:413.535
Hs Code.:

Synonyms:(R)-3-(N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)sulfamoyl)propyl acetate

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Chemical Property of (R)-3-(N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)sulfamoyl)propyl acetate

Chemical Property:

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Technology Process of (R)-3-(N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)sulfamoyl)propyl acetate

There total 3 articles about (R)-3-(N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)sulfamoyl)propyl acetate 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: 79.0%

: 1380335-93-2
(R)-3-chloro-N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)propane-1-sulfonamide

: 127-09-3
sodium acetate

: 1380335-96-5
(R)-3-(N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)sulfamoyl)propyl acetate

Guidance literature:: With sodium iodide; In N,N-dimethyl-formamide; at 20 - 90 ℃; for 6h; Inert atmosphere;
DOI:10.1021/jm300416h

Reference yield:

: 1309653-53-9
(S)-N-((R)-1-(3-(cyclopentyloxy)phenyl)ethyl)-2-methylpropane-2-sulfinamide

: 1380335-96-5
(R)-3-(N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)sulfamoyl)propyl acetate

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / 1,4-dioxane; methanol / 0.5 h / 20 °C / Inert atmosphere

2: triethylamine / dichloromethane / 4 h / 0 - 20 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 20 - 45 °C / Inert atmosphere

4: sodium iodide / N,N-dimethyl-formamide / 6 h / 20 - 90 °C / Inert atmosphere

With hydrogenchloride; triethylamine; N-ethyl-N,N-diisopropylamine; sodium iodide; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm300416h

Reference yield:

: 1198223-03-8
(R)-1-(3-(cyclopentyloxy)phenyl)ethan-1-amine hydrochloride

: 1380335-96-5
(R)-3-(N-(1-(3-(cyclopentyloxy)phenyl)ethyl)-N-(methoxymethyl)sulfamoyl)propyl acetate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 4 h / 0 - 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 20 - 45 °C / Inert atmosphere

3: sodium iodide / N,N-dimethyl-formamide / 6 h / 20 - 90 °C / Inert atmosphere

With triethylamine; N-ethyl-N,N-diisopropylamine; sodium iodide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm300416h