N-[(1S)-1-methoxycarbonylethyl]-2,4,6-trimethyl-N-[(E)-3-phenylprop-2-enyl]phenylsulfonamide

Base Information

Chemical Name:N-[(1S)-1-methoxycarbonylethyl]-2,4,6-trimethyl-N-[(E)-3-phenylprop-2-enyl]phenylsulfonamide
CAS No.:942509-25-3
Molecular Formula:C₂₂H₂₇NO₄S
Molecular Weight:401.527
Hs Code.:

Synonyms:N-[(1S)-1-methoxycarbonylethyl]-2,4,6-trimethyl-N-[(E)-3-phenylprop-2-enyl]phenylsulfonamide

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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-[(1S)-1-methoxycarbonylethyl]-2,4,6-trimethyl-N-[(E)-3-phenylprop-2-enyl]phenylsulfonamide

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Technology Process of N-[(1S)-1-methoxycarbonylethyl]-2,4,6-trimethyl-N-[(E)-3-phenylprop-2-enyl]phenylsulfonamide

There total 2 articles about N-[(1S)-1-methoxycarbonylethyl]-2,4,6-trimethyl-N-[(E)-3-phenylprop-2-enyl]phenylsulfonamide 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: 55.0%

: 59724-80-0
methyl (2S)-2-[(2,4,6-trimethylphenylsulfonyl)amino]propanoate

: 4392-24-9
Cinnamyl bromide

: 942509-25-3
N-[(1S)-1-methoxycarbonylethyl]-2,4,6-trimethyl-N-[(E)-3-phenylprop-2-enyl]phenylsulfonamide

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 2h;
DOI:10.1021/jo0700528

Reference yield:

: 773-64-8
2-mesitylenesulphonyl chloride

: 942509-25-3
N-[(1S)-1-methoxycarbonylethyl]-2,4,6-trimethyl-N-[(E)-3-phenylprop-2-enyl]phenylsulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 46 percent / Et₃N / dimethylformamide / 2.5 h / 20 °C

2: 55 percent / NaH / dimethylformamide / 2 h / 20 °C

With sodium hydride; triethylamine; In N,N-dimethyl-formamide;
DOI:10.1021/jo0700528