methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)-N-((4-trifluoromethoxy)benzyl)sulfamoyl)benzoate

Base Information

Chemical Name:methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)-N-((4-trifluoromethoxy)benzyl)sulfamoyl)benzoate
CAS No.:1381785-36-9
Molecular Formula:C₂₄H₂₀F₃N₃O₅S
Molecular Weight:519.501
Hs Code.:

Synonyms:methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)-N-((4-trifluoromethoxy)benzyl)sulfamoyl)benzoate

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Chemical Property of methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)-N-((4-trifluoromethoxy)benzyl)sulfamoyl)benzoate

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Technology Process of methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)-N-((4-trifluoromethoxy)benzyl)sulfamoyl)benzoate

There total 5 articles about methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)-N-((4-trifluoromethoxy)benzyl)sulfamoyl)benzoate 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:

: 1381785-35-8
Methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)sulfamoyl)benzoate

: 50824-05-0
4-trifluoromethoxybenzyl bromide

: 1381785-36-9
methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)-N-((4-trifluoromethoxy)benzyl)sulfamoyl)benzoate

Guidance literature:: Methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)sulfamoyl)benzoate; With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;

4-trifluoromethoxybenzyl bromide; In N,N-dimethyl-formamide; at 20 ℃; for 18h;

Reference yield:

: 1381785-33-6
tert-Butyl (3-methylimidazo[1,2-a]pyridin-2-yl)carbamate

: 1381785-36-9
methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)-N-((4-trifluoromethoxy)benzyl)sulfamoyl)benzoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0.33 h / 0 °C

1.2: 2 h / 20 °C

2.1: hydrogenchloride / 1,4-dioxane / 18 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C

3.2: 18 h / 20 °C

With hydrogenchloride; sodium hydride; potassium carbonate; In 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 1038828-20-4
ethyl 3-methyl H-imidazo[1,2-a]pyridine-2-carboxylate

: 1381785-36-9
methyl 4-(N-(3-methylimidazo[1,2-a]pyridin-2-yl)-N-((4-trifluoromethoxy)benzyl)sulfamoyl)benzoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide / methanol / 18 h / Reflux

1.2: pH 7

2.1: N-ethyl-N,N-diisopropylamine; diphenylphosphoranyl azide / 1,2-dichloro-ethane / 18 h / 20 °C

2.2: 82 °C

3.1: sodium hydride / N,N-dimethyl-formamide / 0.33 h / 0 °C

3.2: 2 h / 20 °C

4.1: hydrogenchloride / 1,4-dioxane / 18 h / 20 °C

5.1: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C

5.2: 18 h / 20 °C

With hydrogenchloride; diphenylphosphoranyl azide; sodium hydride; potassium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In 1,4-dioxane; methanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;