methyl (S)-4-(5-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate

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Chemical Name:methyl (S)-4-(5-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate
CAS No.:1276687-87-6
Molecular Formula:C₃₀H₃₀F₃N₃O₄
Molecular Weight:553.581
Hs Code.:

Synonyms:methyl (S)-4-(5-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate

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Chemical Property of methyl (S)-4-(5-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate

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Technology Process of methyl (S)-4-(5-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate

There total 9 articles about methyl (S)-4-(5-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate 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:

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 1276687-89-8
C₂₉H₂₈F₃N₃O₄

: 1276687-87-6
methyl (S)-4-(5-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; In methanol; dichloromethane; water; at 20 ℃; for 1h;
DOI:10.1021/jm1011726

Reference yield:

: 1276687-75-2
methyl (S)-4-nitro-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate

: 1276687-87-6
methyl (S)-4-(5-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate

Guidance literature:: Multi-step reaction with 7 steps

1: palladium 10% on activated carbon; hydrogen / methanol; water / 20 °C

2: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 60 °C

3: hydrogen; pyridinium p-toluenesulfonate / ethyl acetate / 20 °C

4: trifluoroacetic acid / dichloromethane / 0 - 20 °C

5: di-tert-butyl-diazodicarboxylate; triphenylphosphine / dichloromethane / 0 - 20 °C

6: trifluoroacetic acid / dichloromethane / 2.5 h / 0 °C

7: sodium tris(acetoxy)borohydride; acetic acid / methanol; dichloromethane; water / 1 h / 20 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; di-tert-butyl-diazodicarboxylate; palladium 10% on activated carbon; hydrogen; pyridinium p-toluenesulfonate; sodium tris(acetoxy)borohydride; caesium carbonate; acetic acid; triphenylphosphine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; trifluoroacetic acid; In 1,4-dioxane; methanol; dichloromethane; water; ethyl acetate; 2: Buchwald-Hartwig reaction / 5: Mitsunobu reaction;
DOI:10.1021/jm1011726

Reference yield:

: 1276687-80-9
methyl (S)-4-(4-(4-methoxybenzyloxy)-2-nitrophenylamino)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate

: 1276687-87-6
methyl (S)-4-(5-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-2-(1-(2-(trifluoromethyl)phenyl)ethoxy)benzoate

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogen; pyridinium p-toluenesulfonate / ethyl acetate / 20 °C

2: trifluoroacetic acid / dichloromethane / 0 - 20 °C

3: di-tert-butyl-diazodicarboxylate; triphenylphosphine / dichloromethane / 0 - 20 °C

4: trifluoroacetic acid / dichloromethane / 2.5 h / 0 °C

5: sodium tris(acetoxy)borohydride; acetic acid / methanol; dichloromethane; water / 1 h / 20 °C

With di-tert-butyl-diazodicarboxylate; hydrogen; pyridinium p-toluenesulfonate; sodium tris(acetoxy)borohydride; acetic acid; triphenylphosphine; trifluoroacetic acid; In methanol; dichloromethane; water; ethyl acetate; 3: Mitsunobu reaction;
DOI:10.1021/jm1011726