[3-({(R)-1-[((R)-1-Hydroxymethyl-2-phenyl-ethyl)-methyl-carbamoyl]-2-naphthalen-2-yl-ethyl}-methyl-carbamoyl)-benzyl]-carbamic acid tert-butyl ester

Base Information

• Chemical Name: [3-({(R)-1-[((R)-1-Hydroxymethyl-2-phenyl-ethyl)-methyl-carbamoyl]-2-naphthalen-2-yl-ethyl}-methyl-carbamoyl)-benzyl]-carbamic acid tert-butyl ester
• CAS No.: 186841-30-5
• Molecular Formula: C₃₇H₄₃N₃O₅
• Molecular Weight: 609.766
• Mol file: 186841-30-5.mol

Synonyms:

Chemical Property of [3-({(R)-1-[((R)-1-Hydroxymethyl-2-phenyl-ethyl)-methyl-carbamoyl]-2-naphthalen-2-yl-ethyl}-methyl-carbamoyl)-benzyl]-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [3-({(R)-1-[((R)-1-Hydroxymethyl-2-phenyl-ethyl)-methyl-carbamoyl]-2-naphthalen-2-yl-ethyl}-methyl-carbamoyl)-benzyl]-carbamic acid tert-butyl ester

There total 5 articles about [3-({(R)-1-[((R)-1-Hydroxymethyl-2-phenyl-ethyl)-methyl-carbamoyl]-2-naphthalen-2-yl-ethyl}-methyl-carbamoyl)-benzyl]-carbamic acid tert-butyl 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:

(2R)-2-(N-(tert-butoxycarbonyl)-N-methylamino)-3-(2-naphthyl)-propionic acid (147577-61-5) → [3-({(R)-1-[((R)-1-Hydroxymethyl-2-phenyl-ethyl)-methyl-carbamoyl]-2-naphthalen-2-yl-ethyl}-methyl-carbamoyl)-benzyl]-carbamic acid tert-butyl ester (186841-30-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 1-hydroxy-7-azabenzotriazole, 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide hydrochloride / dimethylformamide; CH₂Cl₂ / 19 h / 0 - 20 °C

2: CF₃COOH / CH₂Cl₂ / 0.17 h

3: diisopropylethylamine / CH₂Cl₂ / 20 h / Ambient temperature

With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/jm9801962

Reference yield:

(2R)-2-(Methylamino)-3-phenylpropan-1-ol (102339-81-1) → [3-({(R)-1-[((R)-1-Hydroxymethyl-2-phenyl-ethyl)-methyl-carbamoyl]-2-naphthalen-2-yl-ethyl}-methyl-carbamoyl)-benzyl]-carbamic acid tert-butyl ester (186841-30-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 1-hydroxy-7-azabenzotriazole, 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide hydrochloride / dimethylformamide; CH₂Cl₂ / 19 h / 0 - 20 °C

2: CF₃COOH / CH₂Cl₂ / 0.17 h

3: diisopropylethylamine / CH₂Cl₂ / 20 h / Ambient temperature

With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/jm9801962

Reference yield:

3-(tert-butoxycarbonylamino-methyl)benzoic acid (117445-22-4) → [3-({(R)-1-[((R)-1-Hydroxymethyl-2-phenyl-ethyl)-methyl-carbamoyl]-2-naphthalen-2-yl-ethyl}-methyl-carbamoyl)-benzyl]-carbamic acid tert-butyl ester (186841-30-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide hydrochloride / CH₂Cl₂; dimethylformamide / 0.17 h

2: diisopropylethylamine / CH₂Cl₂ / 20 h / Ambient temperature

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/jm9801962

upstream raw materials:

(R)-N-((R)-1-Hydroxymethyl-2-phenyl-ethyl)-N-methyl-2-methylamino-3-naphthalen-2-yl-propionamide

(2R)-2-(N-(tert-butoxycarbonyl)-N-methylamino)-3-(2-naphthyl)-propionic acid

(2R)-2-(Methylamino)-3-phenylpropan-1-ol

3-(tert-butoxycarbonylamino-methyl)benzoic acid