(2S,4R)-4-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)piperidine-2-carboxylic acid

Base Information

Chemical Name:(2S,4R)-4-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)piperidine-2-carboxylic acid
CAS No.:1448667-68-2
Molecular Formula:C₃₀H₃₀N₂O₃
Molecular Weight:466.58
Hs Code.:

Synonyms:(2S,4R)-4-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)piperidine-2-carboxylic acid

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Chemical Property of (2S,4R)-4-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)piperidine-2-carboxylic acid

Chemical Property:

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Technology Process of (2S,4R)-4-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)piperidine-2-carboxylic acid

There total 9 articles about (2S,4R)-4-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)piperidine-2-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: 60.0%

: 1448668-07-2
C₃₁H₃₂N₂O₃

: 1448667-68-2
(2S,4R)-4-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)piperidine-2-carboxylic acid

Guidance literature:: With lithium hydroxide monohydrate; water; In tetrahydrofuran; at 20 ℃;

Reference yield:

: 1871-76-7
diphenylacetic acid chloride

: 1448667-68-2
(2S,4R)-4-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)piperidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 0.25 h / 0 °C

2: 10% palladium hydroxide on charcoal; hydrogen / isopropyl alcohol / 30 °C

3: caesium carbonate / N,N-dimethyl-formamide / 35 °C

4: lithium hydroxide monohydrate; water / tetrahydrofuran / 20 °C

With lithium hydroxide monohydrate; 10% palladium hydroxide on charcoal; water; hydrogen; caesium carbonate; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 1799811-83-8
1-(tert-butyl)-2-methyl-(S)-4-oxopiperidine-1,2-dicarboxylate

: 1448667-68-2
(2S,4R)-4-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)piperidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: acetic acid / methanol / 1 h / 20 °C

1.2: 0 - 20 °C

2.1: hydrogenchloride / methanol / 20 °C

3.1: triethylamine / dichloromethane / 0.25 h / 0 °C

4.1: 10% palladium hydroxide on charcoal; hydrogen / isopropyl alcohol / 30 °C

5.1: caesium carbonate / N,N-dimethyl-formamide / 35 °C

6.1: lithium hydroxide monohydrate; water / tetrahydrofuran / 20 °C

With hydrogenchloride; lithium hydroxide monohydrate; 10% palladium hydroxide on charcoal; water; hydrogen; caesium carbonate; acetic acid; triethylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;