N-(1-(2-((1-methyl-1H-benzo[d]imidazol-2-yl)amino)ethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide

Base Information

Chemical Name:N-(1-(2-((1-methyl-1H-benzo[d]imidazol-2-yl)amino)ethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide
CAS No.:1394161-83-1
Molecular Formula:C₂₄H₂₃N₇O₂
Molecular Weight:441.492
Hs Code.:

Synonyms:N-(1-(2-((1-methyl-1H-benzo[d]imidazol-2-yl)amino)ethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide

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Chemical Property of N-(1-(2-((1-methyl-1H-benzo[d]imidazol-2-yl)amino)ethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide

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Technology Process of N-(1-(2-((1-methyl-1H-benzo[d]imidazol-2-yl)amino)ethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide

There total 4 articles about N-(1-(2-((1-methyl-1H-benzo[d]imidazol-2-yl)amino)ethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-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:

: 1394162-64-1
N-(1-(2-oxoethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide

: 1622-57-7
2-Amino-1-methylbenzimidazole

: 1394161-83-1
N-(1-(2-((1-methyl-1H-benzo[d]imidazol-2-yl)amino)ethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; In dichloromethane; acetonitrile; at 20 ℃; for 18h;

Reference yield:

: 1394162-03-8
1-(2,2-dimethoxyethyl)-4-nitro-1H-pyrazole

: 1394161-83-1
N-(1-(2-((1-methyl-1H-benzo[d]imidazol-2-yl)amino)ethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen / platinum(IV) oxide / ethyl acetate; ethanol / 3 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / dichloromethane / 0.5 h / 20 °C

2.2: 1 h / 20 °C

3.1: hydrogenchloride; water / tetrahydrofuran / 1.5 h / 80 °C

3.2: 20 °C

4.1: sodium tris(acetoxy)borohydride / acetic acid / dichloromethane; acetonitrile / 18 h / 20 °C

With hydrogenchloride; water; hydrogen; sodium tris(acetoxy)borohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; platinum(IV) oxide; acetic acid; In tetrahydrofuran; ethanol; dichloromethane; ethyl acetate; acetonitrile;

Reference yield:

: 1394162-63-0
N-(1-(2,2-dimethoxyethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide

: 1394161-83-1
N-(1-(2-((1-methyl-1H-benzo[d]imidazol-2-yl)amino)ethyl)-1H-pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogenchloride; water / tetrahydrofuran / 1.5 h / 80 °C

1.2: 20 °C

2.1: sodium tris(acetoxy)borohydride / acetic acid / dichloromethane; acetonitrile / 18 h / 20 °C

With hydrogenchloride; water; sodium tris(acetoxy)borohydride; acetic acid; In tetrahydrofuran; dichloromethane; acetonitrile;