2-((3,5-dichloropyridin-4-yl)amino)-N-(4-fluorobenzyl)-7-methyl-1H-benzofuro[4,5-d]imidazole-5-carboxamide

Base Information

Chemical Name:2-((3,5-dichloropyridin-4-yl)amino)-N-(4-fluorobenzyl)-7-methyl-1H-benzofuro[4,5-d]imidazole-5-carboxamide
CAS No.:1374296-13-5
Molecular Formula:C₂₃H₁₆Cl₂FN₅O₂
Molecular Weight:484.317
Hs Code.:

Synonyms:2-((3,5-dichloropyridin-4-yl)amino)-N-(4-fluorobenzyl)-7-methyl-1H-benzofuro[4,5-d]imidazole-5-carboxamide

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Chemical Property of 2-((3,5-dichloropyridin-4-yl)amino)-N-(4-fluorobenzyl)-7-methyl-1H-benzofuro[4,5-d]imidazole-5-carboxamide

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Technology Process of 2-((3,5-dichloropyridin-4-yl)amino)-N-(4-fluorobenzyl)-7-methyl-1H-benzofuro[4,5-d]imidazole-5-carboxamide

There total 9 articles about 2-((3,5-dichloropyridin-4-yl)amino)-N-(4-fluorobenzyl)-7-methyl-1H-benzofuro[4,5-d]imidazole-5-carboxamide 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:

: 1374298-27-7
2-[(3,5-dichloropyridin-4-yl)amino]-7-methyl-1H-furo[3,2-e]benzimidazole-5-carboxylic acid

: 140-75-0
para-fluorobenzylamine

: 1374296-13-5
2-((3,5-dichloropyridin-4-yl)amino)-N-(4-fluorobenzyl)-7-methyl-1H-benzofuro[4,5-d]imidazole-5-carboxamide

Guidance literature:: 2-[(3,5-dichloropyridin-4-yl)amino]-7-methyl-1H-furo[3,2-e]benzimidazole-5-carboxylic acid; With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate;

para-fluorobenzylamine; at 20 ℃;
DOI:10.1016/j.bmcl.2017.10.062

Reference yield:

: 82378-91-4
4-acetamido-2-hydroxy-5-nitrobenzoic acid

: 1374296-13-5
2-((3,5-dichloropyridin-4-yl)amino)-N-(4-fluorobenzyl)-7-methyl-1H-benzofuro[4,5-d]imidazole-5-carboxamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: sulfuric acid / Reflux

2.1: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 80 °C

2.2: 8 h / 80 °C

3.1: cesium fluoride / 24 h / 230 °C

4.1: iron; hydrogenchloride / water / 0 - 20 °C

5.1: acetonitrile / 24 h / 20 °C

5.2: 20 °C

6.1: sodium hydroxide; water / methanol / 60 °C

7.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate

7.2: 20 °C

With hydrogenchloride; sulfuric acid; water; iron; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; cesium fluoride; sodium hydroxide; In methanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.bmcl.2017.10.062

Reference yield:

: 106125-55-7
methyl 4-amino-2-hydroxy-5-nitrobenzoate

: 1374296-13-5
2-((3,5-dichloropyridin-4-yl)amino)-N-(4-fluorobenzyl)-7-methyl-1H-benzofuro[4,5-d]imidazole-5-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 80 °C

1.2: 8 h / 80 °C

2.1: cesium fluoride / 24 h / 230 °C

3.1: iron; hydrogenchloride / water / 0 - 20 °C

4.1: acetonitrile / 24 h / 20 °C

4.2: 20 °C

5.1: sodium hydroxide; water / methanol / 60 °C

6.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate

6.2: 20 °C

With hydrogenchloride; water; iron; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; cesium fluoride; sodium hydroxide; In methanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.bmcl.2017.10.062