(S)-1-(3,3-Dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid (R)-1-(3-carboxymethoxy-phenyl)-3-morpholin-4-yl-propyl ester

Base Information

• Chemical Name: (S)-1-(3,3-Dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid (R)-1-(3-carboxymethoxy-phenyl)-3-morpholin-4-yl-propyl ester
• CAS No.: 769103-72-2
• Molecular Formula: C₂₈H₄₀N₂O₈
• Molecular Weight: 532.634
• Mol file: 769103-72-2.mol

Synonyms:(S)-1-(3,3-Dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid (R)-1-(3-carboxymethoxy-phenyl)-3-morpholin-4-yl-propyl ester

Chemical Property of (S)-1-(3,3-Dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid (R)-1-(3-carboxymethoxy-phenyl)-3-morpholin-4-yl-propyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-1-(3,3-Dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid (R)-1-(3-carboxymethoxy-phenyl)-3-morpholin-4-yl-propyl ester

There total 4 articles about (S)-1-(3,3-Dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid (R)-1-(3-carboxymethoxy-phenyl)-3-morpholin-4-yl-propyl 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: 95.0%

(1R)-1-[3-[2-(1,1-dimethylethoxy)-2-oxoethoxy]phenyl-3-(4-morpholinyl)-1-propanyl (2S)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-piperidinecarboxylate (215168-82-4) → (S)-1-(3,3-Dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid (R)-1-(3-carboxymethoxy-phenyl)-3-morpholin-4-yl-propyl ester (769103-72-2)

Guidance literature:

With hydrogenchloride; In dichloromethane; at 20 ℃; for 2h; Acid hydrolysis;

DOI:10.1016/S0968-0896(98)00125-4

Reference yield:

1-(3-hydroxyphenyl)-3-(4-morpholinyl)-1-propanone (195202-11-0) → (S)-1-(3,3-Dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid (R)-1-(3-carboxymethoxy-phenyl)-3-morpholin-4-yl-propyl ester (769103-72-2)

Guidance literature:

Multi-step reaction with 4 steps

1: 67 percent / K₂CO₃ / acetone / 20 h / 20 °C

2: 27 percent / (+)-DIP-chloride / tetrahydrofuran / -20 °C

3: 72 percent / DMAP; DCC / CH₂Cl₂ / 2 h / 20 °C

4: 95 percent / HCl / CH₂Cl₂ / 2 h / 20 °C / Acid hydrolysis

With hydrogenchloride; dmap; potassium carbonate; dicyclohexyl-carbodiimide; B-chlorodiisopinocampheylborane; In tetrahydrofuran; dichloromethane; acetone; 1: Alkylation / 2: Reduction / 3: Condensation / 4: Hydrolysis;

DOI:10.1016/S0968-0896(98)00125-4

Reference yield:

[3-(3-morpholin-4-yl-propionyl)-phenoxy]-acetic acid tert-butyl ester (195202-12-1) → (S)-1-(3,3-Dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid (R)-1-(3-carboxymethoxy-phenyl)-3-morpholin-4-yl-propyl ester (769103-72-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 27 percent / (+)-DIP-chloride / tetrahydrofuran / -20 °C

2: 72 percent / DMAP; DCC / CH₂Cl₂ / 2 h / 20 °C

3: 95 percent / HCl / CH₂Cl₂ / 2 h / 20 °C / Acid hydrolysis

With hydrogenchloride; dmap; dicyclohexyl-carbodiimide; B-chlorodiisopinocampheylborane; In tetrahydrofuran; dichloromethane; 1: Reduction / 2: Condensation / 3: Hydrolysis;

DOI:10.1016/S0968-0896(98)00125-4

upstream raw materials:

(1R)-1-[3-[2-(1,1-dimethylethoxy)-2-oxoethoxy]phenyl-3-(4-morpholinyl)-1-propanyl (2S)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-piperidinecarboxylate

1-(3-hydroxyphenyl)-3-(4-morpholinyl)-1-propanone

[3-(3-morpholin-4-yl-propionyl)-phenoxy]-acetic acid tert-butyl ester

(R)-1,1-dimethylethyl [3-[1-hydroxy-3-(4-morpholinyl)propyl]phenoxy]acetate