4-(3-chlorobenzo[b]thiophene-2-carboxamido)-3-(5-methylthiazol-2-ylcarbamoyl)benzoic acid

Base Information

Chemical Name:4-(3-chlorobenzo[b]thiophene-2-carboxamido)-3-(5-methylthiazol-2-ylcarbamoyl)benzoic acid
CAS No.:1374778-43-4
Molecular Formula:C₂₁H₁₄ClN₃O₄S₂
Molecular Weight:471.945
Hs Code.:

Synonyms:4-(3-chlorobenzo[b]thiophene-2-carboxamido)-3-(5-methylthiazol-2-ylcarbamoyl)benzoic acid

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Chemical Property of 4-(3-chlorobenzo[b]thiophene-2-carboxamido)-3-(5-methylthiazol-2-ylcarbamoyl)benzoic acid

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Technology Process of 4-(3-chlorobenzo[b]thiophene-2-carboxamido)-3-(5-methylthiazol-2-ylcarbamoyl)benzoic acid

There total 7 articles about 4-(3-chlorobenzo[b]thiophene-2-carboxamido)-3-(5-methylthiazol-2-ylcarbamoyl)benzoic 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: 21.0%

: 1374779-86-8
C₂₂H₁₆ClN₃O₄S₂

: 1374778-43-4
4-(3-chlorobenzo[b]thiophene-2-carboxamido)-3-(5-methylthiazol-2-ylcarbamoyl)benzoic acid

Guidance literature:: With water; lithium hydroxide; In tetrahydrofuran; at 20 ℃;

Reference yield:

: 4315-09-7
4-nitroisophthalic acid

: 1374778-43-4
4-(3-chlorobenzo[b]thiophene-2-carboxamido)-3-(5-methylthiazol-2-ylcarbamoyl)benzoic acid

Guidance literature:: Multi-step reaction with 6 steps

1: sulfuric acid / methanol / 4 h / Reflux

2: hydrogen / palladium 10% on activated carbon / methanol / 20 h

3: tetrahydrofuran / 24 h / Reflux

4: dmap / N,N-dimethyl-formamide / 10 h / 70 - 80 °C

5: tetrahydrofuran / 12 h / Reflux

6: water; lithium hydroxide / tetrahydrofuran / 20 °C

With sulfuric acid; water; hydrogen; lithium hydroxide; dmap; palladium 10% on activated carbon; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;

Reference yield:

: 89-87-2,156617-89-9,37551-97-6
2,4-dimethylnitrobenzene

: 1374778-43-4
4-(3-chlorobenzo[b]thiophene-2-carboxamido)-3-(5-methylthiazol-2-ylcarbamoyl)benzoic acid

Guidance literature:: Multi-step reaction with 7 steps

1: potassium permanganate / water / 90 °C

2: sulfuric acid / methanol / 4 h / Reflux

3: hydrogen / palladium 10% on activated carbon / methanol / 20 h

4: tetrahydrofuran / 24 h / Reflux

5: dmap / N,N-dimethyl-formamide / 10 h / 70 - 80 °C

6: tetrahydrofuran / 12 h / Reflux

7: water; lithium hydroxide / tetrahydrofuran / 20 °C

With potassium permanganate; sulfuric acid; water; hydrogen; lithium hydroxide; dmap; palladium 10% on activated carbon; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;