N-(4-(3-chlorophenyl)thiophen-2-yl)-2-(4-(methylsulfonyl)phenyl)acetamide

Base Information

Chemical Name:N-(4-(3-chlorophenyl)thiophen-2-yl)-2-(4-(methylsulfonyl)phenyl)acetamide
CAS No.:1391982-04-9
Molecular Formula:C₁₉H₁₆ClNO₃S₂
Molecular Weight:405.926
Hs Code.:

Synonyms:N-(4-(3-chlorophenyl)thiophen-2-yl)-2-(4-(methylsulfonyl)phenyl)acetamide

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Chemical Property of N-(4-(3-chlorophenyl)thiophen-2-yl)-2-(4-(methylsulfonyl)phenyl)acetamide

Chemical Property:

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Technology Process of N-(4-(3-chlorophenyl)thiophen-2-yl)-2-(4-(methylsulfonyl)phenyl)acetamide

There total 4 articles about N-(4-(3-chlorophenyl)thiophen-2-yl)-2-(4-(methylsulfonyl)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:

: 1391981-99-9
4-(3-chlorophenyl)thiophen-2-amine hydrochloride

: 90536-66-6
4-(methylsulfonyl)phenylacetic acid

: 1391982-04-9
N-(4-(3-chlorophenyl)thiophen-2-yl)-2-(4-(methylsulfonyl)phenyl)acetamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; Inert atmosphere; Reflux;

Reference yield:

: 99-02-5
3'-Chloroacetophenone

: 1391982-04-9
N-(4-(3-chlorophenyl)thiophen-2-yl)-2-(4-(methylsulfonyl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: morpholine; sulfur / ethanol / Reflux

2.1: ethanol; potassium hydroxide / 20 h / Reflux

2.2: pH 7

3.1: hydrogenchloride / ethanol; water / 2 h / 20 °C

4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Inert atmosphere; Reflux

With morpholine; hydrogenchloride; ethanol; benzotriazol-1-ol; sulfur; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In ethanol; dichloromethane; water;

Reference yield:

: 473438-03-8
ethyl 2-amino-4-(3-chlorophenyl)-thiophene-3-carboxylate

: 1391982-04-9
N-(4-(3-chlorophenyl)thiophen-2-yl)-2-(4-(methylsulfonyl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanol; potassium hydroxide / 20 h / Reflux

1.2: pH 7

2.1: hydrogenchloride / ethanol; water / 2 h / 20 °C

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Inert atmosphere; Reflux

With hydrogenchloride; ethanol; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In ethanol; dichloromethane; water;