5-chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide methanesulfonate

Base Information

Chemical Name:5-chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide methanesulfonate
CAS No.:1312422-72-2
Molecular Formula:CH₄O₃S*C₂₀H₁₅ClN₄O₂S
Molecular Weight:506.991
Hs Code.:

Synonyms:5-chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide methanesulfonate

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Chemical Property of 5-chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide methanesulfonate

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Technology Process of 5-chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide methanesulfonate

There total 4 articles about 5-chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide methanesulfonate 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: 95.0%

: 5-Chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide

: 1312422-72-2
5-chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide methanesulfonate

Guidance literature:: With methanesulfonic acid; In tetrahydrofuran; butanone; at 20 - 50 ℃; for 1.5h; Industry scale;

Reference yield: 95.0%

: 5-Chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide

: 75-75-2,98527-29-8
methanesulfonic acid

: 1312422-72-2
5-chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide methanesulfonate

Guidance literature:: In tetrahydrofuran; butanone; at 20 - 50 ℃; for 1.5h; Product distribution / selectivity;

Reference yield:

: 24065-33-6
5-Chlorothiophene-2-carboxylic acid

: 1312422-72-2
5-chloro-N-((1-(4-(2-oxopyridin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide methanesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / 16 h / 64 °C / Industry scale; Inert atmosphere

2.1: ammonium hydroxide / n-heptane / 20 °C / Industry scale

3.1: toluene / 0.25 h / Industry scale

3.2: 4 h / 100 °C / Industry scale

3.3: 1.25 h / 15 - 35 °C / Industry scale

4.1: butanone; tetrahydrofuran / 1.5 h / 20 - 50 °C / Industry scale

With ammonium hydroxide; sulfuric acid; In tetrahydrofuran; n-heptane; toluene; butanone;