3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid

Base Information

Chemical Name:3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid
CAS No.:1309852-77-4
Molecular Formula:C₂₁H₂₁Cl₂NO₃S
Molecular Weight:438.375
Hs Code.:

Synonyms:3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid

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Chemical Property of 3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid

Chemical Property:

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Technology Process of 3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid

There total 4 articles about 3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid 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:

: 1309853-34-6
3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid methyl ester

: 1309852-77-4
3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid

Guidance literature:: 3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid methyl ester; With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; at 20 ℃; for 16h;

With hydrogenchloride; In water; pH=3;

Reference yield:

: 107818-55-3
3-amino-5-bromo-thiophene-2-carboxylic acid methyl ester

: 1309852-77-4
3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium tris(acetoxy)borohydride; acetic acid / 1,2-dichloro-ethane / 20 °C

2.1: N-chloro-succinimide; triphenylphosphine / dichloromethane / 16 h / 20 °C / Reflux

3.1: triethylamine / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide / N,N-dimethyl-formamide / 24 h / 60 °C

4.1: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 16 h / 20 °C

4.2: pH 3

With N-chloro-succinimide; lithium hydroxide monohydrate; water; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; triphenylphosphine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; In tetrahydrofuran; methanol; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: 478028-33-0
5-bromo-3-isopropylamino-thiophene-2-carboxylic acid methyl ester

: 1309852-77-4
3-[(2,4-dichlorobenzoyl)isopropylamino]-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-chloro-succinimide; triphenylphosphine / dichloromethane / 16 h / 20 °C / Reflux

2.1: triethylamine / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide / N,N-dimethyl-formamide / 24 h / 60 °C

3.1: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 16 h / 20 °C

3.2: pH 3

With N-chloro-succinimide; lithium hydroxide monohydrate; water; triethylamine; triphenylphosphine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;