methyl 3-(N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)sulfamoyl)thiophene-2-carboxylate

Base Information

Chemical Name:methyl 3-(N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)sulfamoyl)thiophene-2-carboxylate
CAS No.:1404097-64-8
Molecular Formula:C₂₄H₂₄N₄O₇S₂
Molecular Weight:544.609
Hs Code.:

Synonyms:methyl 3-(N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)sulfamoyl)thiophene-2-carboxylate

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Chemical Property of methyl 3-(N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)sulfamoyl)thiophene-2-carboxylate

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Technology Process of methyl 3-(N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)sulfamoyl)thiophene-2-carboxylate

There total 7 articles about methyl 3-(N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)sulfamoyl)thiophene-2-carboxylate 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: 65.0%

: 1404097-62-6
4-(((1-(5-nitropyridin-2-yl)piperidin-4-yl)amino)methyl)benzaldehyde

: 59337-92-7
2-(carbomethoxy)thiophene-3-sulfonyl chloride

: 1404097-64-8
methyl 3-(N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)sulfamoyl)thiophene-2-carboxylate

Guidance literature:: With triethylamine; In dichloromethane; at 20 - 25 ℃;
DOI:10.1021/jm301164y

Reference yield:

: C₁₀H₁₄N₄O₂*C₂HF₃O₂

: 1404097-64-8
methyl 3-(N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)sulfamoyl)thiophene-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / ethanol; water / 25 - 80 °C

2: sodium tetrahydroborate / methanol / 0.5 h / 0 - 60 °C

3: hydrogenchloride / water; acetone / 0.5 h

4: triethylamine / dichloromethane / 20 - 25 °C

With hydrogenchloride; sodium tetrahydroborate; potassium carbonate; triethylamine; In methanol; ethanol; dichloromethane; water; acetone;
DOI:10.1021/jm301164y

Reference yield:

: 4548-45-2
2-chloro-5-nitropyridine

: 1404097-64-8
methyl 3-(N-(4-formylbenzyl)-N-(1-(5-nitropyridin-2-yl)piperidin-4-yl)sulfamoyl)thiophene-2-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 80 °C

2: dichloromethane / 3 h / 0 - 25 °C

3: potassium carbonate / ethanol; water / 25 - 80 °C

4: sodium tetrahydroborate / methanol / 0.5 h / 0 - 60 °C

5: hydrogenchloride / water; acetone / 0.5 h

6: triethylamine / dichloromethane / 20 - 25 °C

With hydrogenchloride; sodium tetrahydroborate; potassium carbonate; triethylamine; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm301164y