(R(S))-2-((1S)-1-[tert-butyl(methyl)oxo-λ6-sulfanylidene]amino-2,2-dimethylpropyl)-4-chloro-N-methylaniline

Base Information

Chemical Name:(R(S))-2-((1S)-1-[tert-butyl(methyl)oxo-λ6-sulfanylidene]amino-2,2-dimethylpropyl)-4-chloro-N-methylaniline
CAS No.:1287718-67-5
Molecular Formula:C₁₇H₂₉ClN₂OS
Molecular Weight:344.949
Hs Code.:

Synonyms:(R(S))-2-((1S)-1-[tert-butyl(methyl)oxo-λ6-sulfanylidene]amino-2,2-dimethylpropyl)-4-chloro-N-methylaniline

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Chemical Property of (R(S))-2-((1S)-1-[tert-butyl(methyl)oxo-λ6-sulfanylidene]amino-2,2-dimethylpropyl)-4-chloro-N-methylaniline

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Technology Process of (R(S))-2-((1S)-1-[tert-butyl(methyl)oxo-λ6-sulfanylidene]amino-2,2-dimethylpropyl)-4-chloro-N-methylaniline

There total 7 articles about (R(S))-2-((1S)-1-[tert-butyl(methyl)oxo-λ6-sulfanylidene]amino-2,2-dimethylpropyl)-4-chloro-N-methylaniline 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: 75.0%

: 1287718-39-1
(R(S))-N-(S)-[1-[5-chloro-2-(methylamino)phenyl]-2,2-dimethylpropyl]-2-methyl-2-propanesulfinamide

: 74-88-4
methyl iodide

: 1287718-67-5
(R(S))-2-((1S)-1-[tert-butyl(methyl)oxo-λ6-sulfanylidene]amino-2,2-dimethylpropyl)-4-chloro-N-methylaniline

Guidance literature:: (R(S))-N-(S)-[1-[5-chloro-2-(methylamino)phenyl]-2,2-dimethylpropyl]-2-methyl-2-propanesulfinamide; With lithium hexamethyldisilazane; In tetrahydrofuran; N,N-dimethyl-formamide; at -20 ℃; for 1h; Inert atmosphere;

methyl iodide; In tetrahydrofuran; N,N-dimethyl-formamide; for 2h; Inert atmosphere;
DOI:10.1021/jo1025767

Reference yield:

: 1313017-13-8
N-[4-chloro-2-(2,2-dimethyl-1-oxopropyl)phenyl]-2,2-dimethylpropanamide

: 1287718-67-5
(R(S))-2-((1S)-1-[tert-butyl(methyl)oxo-λ6-sulfanylidene]amino-2,2-dimethylpropyl)-4-chloro-N-methylaniline

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 20 °C / Inert atmosphere

1.2: 5 h

2.1: hydrogenchloride; water / 12 h / 90 °C

3.1: titanium(IV) tetraethanolate / 12 h / 75 °C / Inert atmosphere

3.2: 0.17 h

4.1: diisobutylaluminium hydride / tetrahydrofuran; hexane / 3 h / -78 °C / Inert atmosphere

5.1: lithium hexamethyldisilazane / tetrahydrofuran; N,N-dimethyl-formamide / 1 h / -20 °C / Inert atmosphere

5.2: 2 h / Inert atmosphere

With hydrogenchloride; titanium(IV) tetraethanolate; water; sodium hydride; diisobutylaluminium hydride; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1021/jo1025767

Reference yield:

: 1287718-22-2
N-[(Z)-1-[5-chloro-2-(methylamino)phenyl]-2,2-dimethylpropylidene]-2-methyl-(R(S))-2-propanesulfinamide

: 1287718-67-5
(R(S))-2-((1S)-1-[tert-butyl(methyl)oxo-λ6-sulfanylidene]amino-2,2-dimethylpropyl)-4-chloro-N-methylaniline

Guidance literature:: Multi-step reaction with 2 steps

1.1: diisobutylaluminium hydride / tetrahydrofuran; hexane / 3 h / -78 °C / Inert atmosphere

2.1: lithium hexamethyldisilazane / tetrahydrofuran; N,N-dimethyl-formamide / 1 h / -20 °C / Inert atmosphere

2.2: 2 h / Inert atmosphere

With diisobutylaluminium hydride; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1021/jo1025767