4-Methyl-benzenesulfinic acid [(1R,2S)-2-benzylamino-3-(4-chloro-phenylsulfanyl)-1-cyano-propyl]-amide

Base Information

Chemical Name:4-Methyl-benzenesulfinic acid [(1R,2S)-2-benzylamino-3-(4-chloro-phenylsulfanyl)-1-cyano-propyl]-amide
CAS No.:594874-66-5
Molecular Formula:C₂₄H₂₄ClN₃OS₂
Molecular Weight:470.059
Hs Code.:

Synonyms:4-Methyl-benzenesulfinic acid [(1R,2S)-2-benzylamino-3-(4-chloro-phenylsulfanyl)-1-cyano-propyl]-amide

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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 4-Methyl-benzenesulfinic acid [(1R,2S)-2-benzylamino-3-(4-chloro-phenylsulfanyl)-1-cyano-propyl]-amide

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Technology Process of 4-Methyl-benzenesulfinic acid [(1R,2S)-2-benzylamino-3-(4-chloro-phenylsulfanyl)-1-cyano-propyl]-amide

There total 2 articles about 4-Methyl-benzenesulfinic acid [(1R,2S)-2-benzylamino-3-(4-chloro-phenylsulfanyl)-1-cyano-propyl]-amide 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: 82.0%

: 106-54-7
p-Chlorothiophenol

: (2R,S_S,αR)-α-(p-toluenesulfinylamino)-α-(1-benzylaziridin-2-yl)acetonitrile

: 594874-66-5
4-Methyl-benzenesulfinic acid [(1R,2S)-2-benzylamino-3-(4-chloro-phenylsulfanyl)-1-cyano-propyl]-amide

Guidance literature:: In dichloromethane; at 20 ℃;
DOI:10.1021/jo034477f

Reference yield:

: 429694-44-0
4-Methyl-benzenesulfinic acid 1-((R)-1-benzyl-aziridin-2-yl)-meth-(E)-ylideneamide

: 594874-66-5
4-Methyl-benzenesulfinic acid [(1R,2S)-2-benzylamino-3-(4-chloro-phenylsulfanyl)-1-cyano-propyl]-amide

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / CsF / tetrahydrofuran / -50 °C

2: 82 percent / CH₂Cl₂ / 20 °C

With cesium fluoride; In tetrahydrofuran; dichloromethane; 1: Strecker reaction;
DOI:10.1021/jo034477f