{1-[2-(2,6-dimethylphenoxy)ethyl]-2-piperidin-1-ylmethyl-1H-benzimidazol-6-yloxy}acetic acid ethyl ester

Base Information

Chemical Name:{1-[2-(2,6-dimethylphenoxy)ethyl]-2-piperidin-1-ylmethyl-1H-benzimidazol-6-yloxy}acetic acid ethyl ester
CAS No.:1446281-88-4
Molecular Formula:C₂₇H₃₅N₃O₄
Molecular Weight:465.593
Hs Code.:

Synonyms:{1-[2-(2,6-dimethylphenoxy)ethyl]-2-piperidin-1-ylmethyl-1H-benzimidazol-6-yloxy}acetic acid ethyl ester

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Chemical Property of {1-[2-(2,6-dimethylphenoxy)ethyl]-2-piperidin-1-ylmethyl-1H-benzimidazol-6-yloxy}acetic acid ethyl ester

Chemical Property:

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Technology Process of {1-[2-(2,6-dimethylphenoxy)ethyl]-2-piperidin-1-ylmethyl-1H-benzimidazol-6-yloxy}acetic acid ethyl ester

There total 6 articles about {1-[2-(2,6-dimethylphenoxy)ethyl]-2-piperidin-1-ylmethyl-1H-benzimidazol-6-yloxy}acetic acid ethyl ester 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:

: 1446282-01-4
ethyl 2-(3-{[2-(2,6-dimethylphenoxy)ethyl]amino}-4-(2-piperidylacetylamino)phenoxy)acetate

: 1446281-88-4
{1-[2-(2,6-dimethylphenoxy)ethyl]-2-piperidin-1-ylmethyl-1H-benzimidazol-6-yloxy}acetic acid ethyl ester

Guidance literature:: With acetic acid; at 100 ℃; for 6h;

Reference yield:

: 610-81-1
4-hydroxy-2-nitroaniline

: 1446281-88-4
{1-[2-(2,6-dimethylphenoxy)ethyl]-2-piperidin-1-ylmethyl-1H-benzimidazol-6-yloxy}acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 2.5 h

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

3: hydrogen; palladium 10% on activated carbon / ethanol / 3.5 h / 2223.8 Torr

4: potassium iodide; potassium carbonate / N,N-dimethyl-formamide / 110 °C

5: acetic acid / 6 h / 100 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; potassium iodide; In ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 59820-64-3
ethyl 2-(4-amino-3-nitrophenoxy)acetate

: 1446281-88-4
{1-[2-(2,6-dimethylphenoxy)ethyl]-2-piperidin-1-ylmethyl-1H-benzimidazol-6-yloxy}acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

2: hydrogen; palladium 10% on activated carbon / ethanol / 3.5 h / 2223.8 Torr

3: potassium iodide; potassium carbonate / N,N-dimethyl-formamide / 110 °C

4: acetic acid / 6 h / 100 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; potassium iodide; In ethanol; dichloromethane; N,N-dimethyl-formamide;