1-(1-(4-fluorobenzyl)-5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide

Base Information

Chemical Name:1-(1-(4-fluorobenzyl)-5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide
CAS No.:1268709-97-2
Molecular Formula:C₂₆H₃₁FN₄O₂
Molecular Weight:450.556
Hs Code.:

Synonyms:1-(1-(4-fluorobenzyl)-5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide

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Chemical Property of 1-(1-(4-fluorobenzyl)-5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide

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Technology Process of 1-(1-(4-fluorobenzyl)-5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide

There total 9 articles about 1-(1-(4-fluorobenzyl)-5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-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: 15.0%

: 1268713-12-7
1-(5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide

: 459-46-1
4-Fluorobenzyl bromide

: 1268709-97-2
1-(1-(4-fluorobenzyl)-5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 120 ℃; for 1h; Microwave irradiation;

Reference yield:

: 29096-75-1,943743-88-2
2-amino-5,6-dimethylbenzimidazole

: 1268709-97-2
1-(1-(4-fluorobenzyl)-5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium nitrite; copper dichloride / water / 2 h / 20 - 100 °C

2: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 3 h / 180 °C / a sealed tube

3: caesium carbonate / N,N-dimethyl-formamide / 1 h / 120 °C / Microwave irradiation

With caesium carbonate; N-ethyl-N,N-diisopropylamine; copper dichloride; sodium nitrite; In 1,4-dioxane; water; N,N-dimethyl-formamide;

Reference yield:

: 1126-09-6
4-carbethoxypiperidine

: 1268709-97-2
1-(1-(4-fluorobenzyl)-5,6-dimethyl-1H-benzo[d]imidazol-2-yl)-N-(tetrahydrofuran-3-yl)piperidine-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1,4-dioxane / 1 h / 180 °C / Microwave irradiation

2.1: sodium hydroxide; water / ethanol / 1 h / 20 °C

2.2: pH 4 - 5

3.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 1 h / 20 °C

4.1: caesium carbonate / N,N-dimethyl-formamide / 1 h / 120 °C / Microwave irradiation

With water; caesium carbonate; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In 1,4-dioxane; ethanol; N,N-dimethyl-formamide;