N-(5-(1H-benzo[d]imidazol-2-yl)-2-methylphenyl)-4-(pyridin-2-ylmethoxy)benzamide

Base Information

Chemical Name:N-(5-(1H-benzo[d]imidazol-2-yl)-2-methylphenyl)-4-(pyridin-2-ylmethoxy)benzamide
CAS No.:1126408-37-4
Molecular Formula:C₂₇H₂₂N₄O₂
Molecular Weight:434.497
Hs Code.:

Synonyms:N-(5-(1H-benzo[d]imidazol-2-yl)-2-methylphenyl)-4-(pyridin-2-ylmethoxy)benzamide

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Chemical Property of N-(5-(1H-benzo[d]imidazol-2-yl)-2-methylphenyl)-4-(pyridin-2-ylmethoxy)benzamide

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Technology Process of N-(5-(1H-benzo[d]imidazol-2-yl)-2-methylphenyl)-4-(pyridin-2-ylmethoxy)benzamide

There total 7 articles about N-(5-(1H-benzo[d]imidazol-2-yl)-2-methylphenyl)-4-(pyridin-2-ylmethoxy)benzamide 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: 99.0%

: 1391913-26-0
N-(2-aminophenyl)-4-methyl-3-(4-(pyridin-2-ylmethoxy)benzamido)benzamide

: 1126408-37-4
N-(5-(1H-benzo[d]imidazol-2-yl)-2-methylphenyl)-4-(pyridin-2-ylmethoxy)benzamide

Guidance literature:: With acetic acid; for 2h; Reflux;
DOI:10.1016/j.bmcl.2012.04.104

Reference yield:

: 1126601-99-7
4-(pyridin-2-ylmethoxy)benzoyl chloride

: 292644-33-8
5(1H-benzoimidazol-2-yl)-2-methyl-phenylamine

: 1126408-37-4
N-(5-(1H-benzo[d]imidazol-2-yl)-2-methylphenyl)-4-(pyridin-2-ylmethoxy)benzamide

Guidance literature:: With pyridine; at 60 ℃; for 1h;

Reference yield:

: 120-47-8
Ethyl 4-hydroxybenzoate

: 1126408-37-4
N-(5-(1H-benzo[d]imidazol-2-yl)-2-methylphenyl)-4-(pyridin-2-ylmethoxy)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / water; acetonitrile

2: sodium hydroxide / ethanol / 20 °C / Reflux

3: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 4 h / 50 °C / Inert atmosphere

4: sodium hydroxide / methanol; water / 2 h / 70 °C

5: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 4 h / 0 - 20 °C

6: acetic acid / 2 h / Reflux

With potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In methanol; ethanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.bmcl.2012.04.104