(R)-1-acetyl-4-(4'-(1-methyl-5-((1-phenylethoxy)carbonylamino)-1H-pyrazol-4-yl)biphenyl-4-yl)piperidine-4-carboxylic acid

Base Information

Chemical Name:(R)-1-acetyl-4-(4'-(1-methyl-5-((1-phenylethoxy)carbonylamino)-1H-pyrazol-4-yl)biphenyl-4-yl)piperidine-4-carboxylic acid
CAS No.:1402465-73-9
Molecular Formula:C₃₃H₃₄N₄O₅
Molecular Weight:566.657
Hs Code.:

Synonyms:(R)-1-acetyl-4-(4'-(1-methyl-5-((1-phenylethoxy)carbonylamino)-1H-pyrazol-4-yl)biphenyl-4-yl)piperidine-4-carboxylic acid

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Chemical Property of (R)-1-acetyl-4-(4'-(1-methyl-5-((1-phenylethoxy)carbonylamino)-1H-pyrazol-4-yl)biphenyl-4-yl)piperidine-4-carboxylic acid

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Technology Process of (R)-1-acetyl-4-(4'-(1-methyl-5-((1-phenylethoxy)carbonylamino)-1H-pyrazol-4-yl)biphenyl-4-yl)piperidine-4-carboxylic acid

There total 9 articles about (R)-1-acetyl-4-(4'-(1-methyl-5-((1-phenylethoxy)carbonylamino)-1H-pyrazol-4-yl)biphenyl-4-yl)piperidine-4-carboxylic acid 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:

: 1402466-00-5
1-acetyl-4-(4-bromophenyl)piperidine-4-carboxylic acid

: 1402465-79-5
(R)-1-phenylethyl 1-methyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-pyrazol-5-ylcarbamate

: 1402465-73-9
(R)-1-acetyl-4-(4'-(1-methyl-5-((1-phenylethoxy)carbonylamino)-1H-pyrazol-4-yl)biphenyl-4-yl)piperidine-4-carboxylic acid

Guidance literature:: 1-acetyl-4-(4-bromophenyl)piperidine-4-carboxylic acid; (R)-1-phenylethyl 1-methyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-pyrazol-5-ylcarbamate; With potassium phosphate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; water; at 100 ℃; for 0.5h; Inert atmosphere; Sealed; microwave irradiation;

With hydrogenchloride; In 1,4-dioxane; water;

Reference yield:

: 16532-79-9
4-Bromophenylacetonitrile

: 1402465-73-9
(R)-1-acetyl-4-(4'-(1-methyl-5-((1-phenylethoxy)carbonylamino)-1H-pyrazol-4-yl)biphenyl-4-yl)piperidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: ethanol / 48 h / 20 °C

2.1: 144 h / -20 - 20 °C

3.1: potassium acetate / tricyclohexylphosphine; bis(dibenzylideneacetone)-palladium⁽⁰⁾ / 1,4-dioxane / 16 h / Reflux

4.1: pyridine / dichloromethane / 0.17 h / 0 - 20 °C

4.2: 16 h / 0 - 20 °C

5.1: potassium phosphate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane; water / 0.5 h / 100 °C / Inert atmosphere; Sealed; microwave irradiation

With pyridine; potassium phosphate; potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; bis(dibenzylideneacetone)-palladium⁽⁰⁾; tricyclohexylphosphine; In 1,4-dioxane; ethanol; dichloromethane; water;

Reference yield:

: 1076197-05-1
4-(4-bromophenyl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid

: 1402465-73-9
(R)-1-acetyl-4-(4'-(1-methyl-5-((1-phenylethoxy)carbonylamino)-1H-pyrazol-4-yl)biphenyl-4-yl)piperidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / 108 h / 20 °C / Reflux

1.2: pH 10

2.1: pyridine / dichloromethane / 3 h / 20 °C

3.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 5 h / 20 °C

3.2: pH 1 - 2

4.1: potassium phosphate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane; water / 0.5 h / 100 °C / Inert atmosphere; Sealed; microwave irradiation

With pyridine; potassium phosphate; lithium hydroxide monohydrate; sulfuric acid; water; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water;