N-(4-(3-chlorophenyl)-5-phenoxythiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

Base Information

Chemical Name:N-(4-(3-chlorophenyl)-5-phenoxythiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide
CAS No.:1391979-69-3
Molecular Formula:C₂₅H₂₁ClN₂O₄S₂
Molecular Weight:513.038
Hs Code.:

Synonyms:N-(4-(3-chlorophenyl)-5-phenoxythiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

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Chemical Property of N-(4-(3-chlorophenyl)-5-phenoxythiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

Chemical Property:

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Technology Process of N-(4-(3-chlorophenyl)-5-phenoxythiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

There total 8 articles about N-(4-(3-chlorophenyl)-5-phenoxythiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide 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: 5.0%

: 383135-47-5
2-[4-(ethanesulfonyl)phenyl]acetic acid

: 1391980-05-4
4-(3-chlorophenyl)-5-phenoxythiazol-2-amine

: 1391979-69-3
N-(4-(3-chlorophenyl)-5-phenoxythiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 35 ℃; for 48h;
DOI:10.1016/j.bmc.2015.07.068

Reference yield:

: 90533-23-6
4-(3-chlorophenyl)-1,3-thiazol-2-amine

: 1391979-69-3
N-(4-(3-chlorophenyl)-5-phenoxythiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide / tetrahydrofuran / 20 °C

2: caesium carbonate / acetone / 45 °C

3: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 48 h / 35 °C

With N-Bromosuccinimide; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1016/j.bmc.2015.07.068

Reference yield:

: 41011-01-2
2-bromo-1-(3-chloro-phenyl)-ethanone

: 1391979-69-3
N-(4-(3-chlorophenyl)-5-phenoxythiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: ethanol / Reflux

2: N-Bromosuccinimide / tetrahydrofuran / 20 °C

3: caesium carbonate / acetone / 45 °C

4: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 48 h / 35 °C

With N-Bromosuccinimide; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; dichloromethane; acetone;
DOI:10.1016/j.bmc.2015.07.068