N-[(1R)-1-phenylpropyl]-1-(2-pyridinylmethyl)-1H-benzimidazole-5-carboxamide

Base Information

Chemical Name:N-[(1R)-1-phenylpropyl]-1-(2-pyridinylmethyl)-1H-benzimidazole-5-carboxamide
CAS No.:1168220-34-5
Molecular Formula:C₂₃H₂₂N₄O
Molecular Weight:370.454
Hs Code.:

Synonyms:N-[(1R)-1-phenylpropyl]-1-(2-pyridinylmethyl)-1H-benzimidazole-5-carboxamide

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Chemical Property of N-[(1R)-1-phenylpropyl]-1-(2-pyridinylmethyl)-1H-benzimidazole-5-carboxamide

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Technology Process of N-[(1R)-1-phenylpropyl]-1-(2-pyridinylmethyl)-1H-benzimidazole-5-carboxamide

There total 5 articles about N-[(1R)-1-phenylpropyl]-1-(2-pyridinylmethyl)-1H-benzimidazole-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:

: 64-18-6
formic acid

: 1168138-77-9
3-amino-N-[(1R)-1-phenylpropyl]-4-[(2-pyridinylmethyl)amino]benzamide

: 1168220-34-5
N-[(1R)-1-phenylpropyl]-1-(2-pyridinylmethyl)-1H-benzimidazole-5-carboxamide

Guidance literature:: formic acid; 3-amino-N-[(1R)-1-phenylpropyl]-4-[(2-pyridinylmethyl)amino]benzamide; at 110 ℃; for 1h;

With sodium hydrogencarbonate; In water; ethyl acetate; pH=8 - 9;

Reference yield:

: 1168138-38-2
4-fluoro-3-nitro-N-[(1R)-1-phenylpropyl]benzamide

: 1168220-34-5
N-[(1R)-1-phenylpropyl]-1-(2-pyridinylmethyl)-1H-benzimidazole-5-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 17 h / Reflux

2: tin(II) chloride dihdyrate / ethyl acetate / 2 h / Reflux

3: 1 h / 110 °C

With tin(II) chloride dihdyrate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethyl acetate;
DOI:10.1016/j.bmcl.2011.06.088

Reference yield:

: 1168138-50-8
3-nitro-N-[(1R)-1-phenylpropyl]-4-[(2-pyridinylmethyl)amino]benzamide

: 1168220-34-5
N-[(1R)-1-phenylpropyl]-1-(2-pyridinylmethyl)-1H-benzimidazole-5-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: tin(II) chloride dihdyrate / ethyl acetate / 2 h / Reflux

2: 1 h / 110 °C

With tin(II) chloride dihdyrate; In ethyl acetate;
DOI:10.1016/j.bmcl.2011.06.088