(2E)-3-[2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-(3-oxobutoxy)phenyl]-N-(pentylsulfonyl)acrylamide

Base Information

Chemical Name:(2E)-3-[2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-(3-oxobutoxy)phenyl]-N-(pentylsulfonyl)acrylamide
CAS No.:926303-27-7
Molecular Formula:C₂₄H₂₆ClF₃N₂O₆S
Molecular Weight:562.994
Hs Code.:

Synonyms:(2E)-3-[2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-(3-oxobutoxy)phenyl]-N-(pentylsulfonyl)acrylamide

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Chemical Property of (2E)-3-[2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-(3-oxobutoxy)phenyl]-N-(pentylsulfonyl)acrylamide

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Technology Process of (2E)-3-[2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-(3-oxobutoxy)phenyl]-N-(pentylsulfonyl)acrylamide

There total 8 articles about (2E)-3-[2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-(3-oxobutoxy)phenyl]-N-(pentylsulfonyl)acrylamide 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: 60.0%

: 926303-26-6
(2E)-3-(2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-[2-(2-methyl-1,3-dioxolan-2-yl)ethoxy]phenyl)-N-(pentylsulfonyl)acrylamide

: 926303-27-7
(2E)-3-[2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-(3-oxobutoxy)phenyl]-N-(pentylsulfonyl)acrylamide

Guidance literature:: With hydrogenchloride; water; In tetrahydrofuran; at 60 ℃; for 1h;
DOI:10.1016/j.bmc.2012.03.036

Reference yield:

: 926295-27-4
ethyl (2E)-3-(2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-hydroxyphenyl)acrylate

: 926303-27-7
(2E)-3-[2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-(3-oxobutoxy)phenyl]-N-(pentylsulfonyl)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 - 80 °C

2.1: sodium hydroxide / tetrahydrofuran; ethanol; water / 0.5 h / 50 °C

2.2: 20 °C

3.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 0 - 20 °C

4.1: hydrogenchloride; water / tetrahydrofuran / 1 h / 60 °C

With hydrogenchloride; dmap; water; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.bmc.2012.03.036

Reference yield:

: 926298-27-3
ethyl (2E)-3-(2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-[2-(2-methyl-1,3-dioxolan-2-yl)ethoxy]phenyl)acrylate

: 926303-27-7
(2E)-3-[2-([3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy)-4-(3-oxobutoxy)phenyl]-N-(pentylsulfonyl)acrylamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / tetrahydrofuran; ethanol; water / 0.5 h / 50 °C

1.2: 20 °C

2.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 0 - 20 °C

3.1: hydrogenchloride; water / tetrahydrofuran / 1 h / 60 °C

With hydrogenchloride; dmap; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; ethanol; water; acetonitrile;
DOI:10.1016/j.bmc.2012.03.036