N-((1R,2R)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-((1R,2R)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)-4-methylbenzenesulfonamide
CAS No.:1242103-61-2
Molecular Formula:C₂₃H₂₆N₂O₃S
Molecular Weight:410.537
Hs Code.:

Synonyms:N-((1R,2R)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)-4-methylbenzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-((1R,2R)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)-4-methylbenzenesulfonamide

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Technology Process of N-((1R,2R)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)-4-methylbenzenesulfonamide

There total 3 articles about N-((1R,2R)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)-4-methylbenzenesulfonamide 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: 92.0%

: 1333982-13-0
N-((1R,2R)-1,2-diphenyl-2-(2-(tetrahydro-2H-pyran-2-yloxy)ethylamino)ethyl)-4-methylbenzenesulfonamide

: 1242103-61-2
N-((1R,2R)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)-4-methylbenzenesulfonamide

Guidance literature:: With hydrogenchloride; water; In ethanol; at 40 ℃; for 2h; Inert atmosphere;
DOI:10.1021/ja207283t

Reference yield: 47.0%

: 1242103-60-1
C₃₉H₄₂N₂O₃SSi

: 1242103-61-2
N-((1R,2R)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)-4-methylbenzenesulfonamide

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1016/j.tetlet.2010.06.017

Reference yield:

: 144222-34-4
(R,R)-N-(p-toluenesulfonyl)-1,2-diphenylethylenediamine

: 1242103-61-2
N-((1R,2R)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: dimethyl sulfoxide / 30 h / 60 °C / Inert atmosphere

2: hydrogenchloride; water / ethanol / 2 h / 40 °C / Inert atmosphere

With hydrogenchloride; water; In ethanol; dimethyl sulfoxide;
DOI:10.1021/ja207283t