N-cyclopropyl-4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzamide

Base Information

Chemical Name:N-cyclopropyl-4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzamide
CAS No.:1401449-65-7
Molecular Formula:C₂₁H₂₄N₄O
Molecular Weight:348.448
Hs Code.:

Synonyms:N-cyclopropyl-4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzamide

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Chemical Property of N-cyclopropyl-4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzamide

Chemical Property:

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Technology Process of N-cyclopropyl-4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzamide

There total 5 articles about N-cyclopropyl-4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}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: 33.8%

: 1401449-55-5
4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzoic acid

: 765-30-0
Cyclopropylamine

: 1401449-65-7
N-cyclopropyl-4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; at 20 ℃; for 4h;

Reference yield:

: 10597-52-1
4-nitro-benzimidazole

: 1401449-65-7
N-cyclopropyl-4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 20 °C

1.2: 15 h / 130 °C

2.1: hydrogen / palladium 10% on activated carbon / ethanol / 26 h / 760.05 Torr

3.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 2 h / 20 °C

4.1: sodium hydroxide; water / ethanol / 24 h / 90 °C

4.2: 20 °C

5.1: N-ethyl-N,N-diisopropylamine; HATU / tetrahydrofuran / 4 h / 20 °C

With water; hydrogen; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1194-02-1,143234-87-1
4-fluorobenzonitrile

: 1401449-65-7
N-cyclopropyl-4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 20 °C

1.2: 15 h / 130 °C

2.1: hydrogen / palladium 10% on activated carbon / ethanol / 26 h / 760.05 Torr

3.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 2 h / 20 °C

4.1: sodium hydroxide; water / ethanol / 24 h / 90 °C

4.2: 20 °C

5.1: N-ethyl-N,N-diisopropylamine; HATU / tetrahydrofuran / 4 h / 20 °C

With water; hydrogen; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;