(S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester

Base Information

• Chemical Name: (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester
• CAS No.: 187851-83-8
• Molecular Formula: C₃₇H₅₀N₂O₉
• Molecular Weight: 666.812
• Mol file: 187851-83-8.mol

Synonyms:(S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester

Chemical Property of (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester

There total 4 articles about (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-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:

benzyl (S)-Lactate (56777-24-3) → (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester (187851-83-8)

Guidance literature:

Multi-step reaction with 3 steps

1: 80 percent / triphenylphosphine; diethyl azodicarboxylate / diethyl ether / 1 h / 20 °C

2: TFA / CH₂Cl₂ / 1.5 h

3: 4 g / diisopropylcarbodiimide; dimethylaminopyridine / CH₂Cl₂ / 16 h / 20 °C

With dmap; triphenylphosphine; trifluoroacetic acid; diisopropyl-carbodiimide; diethylazodicarboxylate; In diethyl ether; dichloromethane;

DOI:10.1016/S0960-894X(01)00748-X

Reference yield:

Boc-L-MeLeu-D-PhLac-OH (153052-71-2) + benzyl L-pipecolyl-D-lactate (187851-82-7) → (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester (187851-83-8)

Guidance literature:

With dmap; diisopropyl-carbodiimide; In dichloromethane; at 20 ℃; for 16h;

DOI:10.1016/S0960-894X(01)00748-X

Reference yield:

(S)-(-)-1-(tert-butoxycarbonyl)-2-piperidinecarboxylic acid (26250-84-0) → (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester (187851-83-8)

Guidance literature:

Multi-step reaction with 3 steps

1: 80 percent / triphenylphosphine; diethyl azodicarboxylate / diethyl ether / 1 h / 20 °C

2: TFA / CH₂Cl₂ / 1.5 h

3: 4 g / diisopropylcarbodiimide; dimethylaminopyridine / CH₂Cl₂ / 16 h / 20 °C

With dmap; triphenylphosphine; trifluoroacetic acid; diisopropyl-carbodiimide; diethylazodicarboxylate; In diethyl ether; dichloromethane;

DOI:10.1016/S0960-894X(01)00748-X

upstream raw materials:

Boc-L-MeLeu-D-PhLac-OH

benzyl L-pipecolyl-D-lactate

benzyl (S)-Lactate

(S)-(-)-1-(tert-butoxycarbonyl)-2-piperidinecarboxylic acid

Downstream raw materials:

(S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-carboxy-ethyl ester