N-(5-(4-chloro-2-(trifluoromethyl)phenoxy)-4-(3-cyanophenyl)thiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

Base Information

Chemical Name:N-(5-(4-chloro-2-(trifluoromethyl)phenoxy)-4-(3-cyanophenyl)thiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide
CAS No.:1391979-79-5
Molecular Formula:C₂₇H₁₉ClF₃N₃O₄S₂
Molecular Weight:606.046
Hs Code.:

Synonyms:N-(5-(4-chloro-2-(trifluoromethyl)phenoxy)-4-(3-cyanophenyl)thiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

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Chemical Property of N-(5-(4-chloro-2-(trifluoromethyl)phenoxy)-4-(3-cyanophenyl)thiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

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Technology Process of N-(5-(4-chloro-2-(trifluoromethyl)phenoxy)-4-(3-cyanophenyl)thiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

There total 11 articles about N-(5-(4-chloro-2-(trifluoromethyl)phenoxy)-4-(3-cyanophenyl)thiazol-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: 11.0%

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

: 1391980-14-5
3-(2-amino-5-(4-chloro-2-(trifluoromethyl)phenoxy)thiazol-4-yl)benzonitrile

: 1391979-79-5
N-(5-(4-chloro-2-(trifluoromethyl)phenoxy)-4-(3-cyanophenyl)thiazol-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 40 ℃; for 12h;
DOI:10.1016/j.bmc.2015.07.068

Reference yield:

: 1535-76-8
4-amino-2-(trifluoromethyl)phenol

: 1391979-79-5
N-(5-(4-chloro-2-(trifluoromethyl)phenoxy)-4-(3-cyanophenyl)thiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium nitrite; hydrogenchloride / acetonitrile; water / 0 °C

1.2: 6 h / 100 °C

2.1: caesium carbonate / acetone / 4 h / 45 °C

3.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 12 h / 40 °C

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

Reference yield:

: 654-76-2
1-methoxy-4-nitro-2-(trifluoromethyl)benzene

: 1391979-79-5
N-(5-(4-chloro-2-(trifluoromethyl)phenoxy)-4-(3-cyanophenyl)thiazol-2-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium chloride; N,N-dimethyl-formamide / 5 h / 160 °C

2.1: zinc; ammonium formate / methanol; water / 3 h / 80 °C

3.1: sodium nitrite; hydrogenchloride / acetonitrile; water / 0 °C

3.2: 6 h / 100 °C

4.1: caesium carbonate / acetone / 4 h / 45 °C

5.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 12 h / 40 °C

With hydrogenchloride; ammonium formate; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; lithium chloride; zinc; sodium nitrite; In methanol; dichloromethane; water; acetone; acetonitrile;
DOI:10.1016/j.bmc.2015.07.068