1,1-dimethylethyl ((1S)-2-{[3-{[(2-chlorophenyl)sulfonyl]amino}-4-(methyloxy)phenyl]amino}-1-methyl-2-oxoethyl)methylcarbamate

Base Information

Chemical Name:1,1-dimethylethyl ((1S)-2-{[3-{[(2-chlorophenyl)sulfonyl]amino}-4-(methyloxy)phenyl]amino}-1-methyl-2-oxoethyl)methylcarbamate
CAS No.:953391-89-4
Molecular Formula:C₂₂H₂₈ClN₃O₆S
Molecular Weight:498
Hs Code.:

Synonyms:1,1-dimethylethyl ((1S)-2-{[3-{[(2-chlorophenyl)sulfonyl]amino}-4-(methyloxy)phenyl]amino}-1-methyl-2-oxoethyl)methylcarbamate

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Chemical Property of 1,1-dimethylethyl ((1S)-2-{[3-{[(2-chlorophenyl)sulfonyl]amino}-4-(methyloxy)phenyl]amino}-1-methyl-2-oxoethyl)methylcarbamate

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Technology Process of 1,1-dimethylethyl ((1S)-2-{[3-{[(2-chlorophenyl)sulfonyl]amino}-4-(methyloxy)phenyl]amino}-1-methyl-2-oxoethyl)methylcarbamate

There total 4 articles about 1,1-dimethylethyl ((1S)-2-{[3-{[(2-chlorophenyl)sulfonyl]amino}-4-(methyloxy)phenyl]amino}-1-methyl-2-oxoethyl)methylcarbamate 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:

: 953391-74-7
N-[5-amino-2-(methyloxy)phenyl]-4-bromo-2-chlorobenzenesulfonamide

: 953391-89-4
1,1-dimethylethyl ((1S)-2-{[3-{[(2-chlorophenyl)sulfonyl]amino}-4-(methyloxy)phenyl]amino}-1-methyl-2-oxoethyl)methylcarbamate

Guidance literature:: N-(tert-butoxycarbonyl)-N-methyl-L-alanine; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.333333h;

N-[5-amino-2-(methyloxy)phenyl]-4-bromo-2-chlorobenzenesulfonamide; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 953391-73-6
4-bromo-2-chloro-N-[2-(methyloxy)-5-nitrophenyl]benzenesulfonamide

: 953391-89-4
1,1-dimethylethyl ((1S)-2-{[3-{[(2-chlorophenyl)sulfonyl]amino}-4-(methyloxy)phenyl]amino}-1-methyl-2-oxoethyl)methylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: ammonium formate / 5 % platinum on carbon / methanol; water / 40 h / 20 °C

2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.33 h / 20 °C

2.2: 20 °C

With ammonium formate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; 5 % platinum on carbon; In methanol; water; N,N-dimethyl-formamide;

Reference yield:

: 351003-52-6
4-bromo-2-chlorobenzene-1-sulfonyl chloride

: 953391-89-4
1,1-dimethylethyl ((1S)-2-{[3-{[(2-chlorophenyl)sulfonyl]amino}-4-(methyloxy)phenyl]amino}-1-methyl-2-oxoethyl)methylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine / dichloromethane / 20 °C

2.1: ammonium formate / 5 % platinum on carbon / methanol; water / 40 h / 20 °C

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.33 h / 20 °C

3.2: 20 °C

With pyridine; ammonium formate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; 5 % platinum on carbon; In methanol; dichloromethane; water; N,N-dimethyl-formamide;