{(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butyl}-carbamic acid tert-butyl ester

Base Information

• Chemical Name: {(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butyl}-carbamic acid tert-butyl ester
• CAS No.: 118792-34-0
• Molecular Formula: C₂₄H₃₇N₃O₅
• Molecular Weight: 447.575

Synonyms:{(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butyl}-carbamic acid tert-butyl ester

Chemical Property of {(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butyl}-carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of {(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butyl}-carbamic acid tert-butyl ester

There total 4 articles about {(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butyl}-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: 81.0%

N-Boc-D-Leu (16937-99-8,53296-34-7) + (R)-N-(4-Acetyl-phenyl)-2-amino-3-methyl-butyramide; hydrobromide → {(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butyl}-carbamic acid tert-butyl ester (118792-34-0)

Guidance literature:

With benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 4 ℃;

DOI:10.1248/cpb.36.3119

Reference yield:

N-[(benzyloxy)carbonyl]-D-valine (1685-33-2) → {(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butyl}-carbamic acid tert-butyl ester (118792-34-0)

Guidance literature:

Multi-step reaction with 3 steps

1: 95 percent / PCl₃, pyridine / Ambient temperature

2: 25percent HBr-AcOH

3: 81 percent / HOBt, DCC, Et₃N / dimethylformamide / 4 °C

With pyridine; hydrogen bromide; benzotriazol-1-ol; acetic acid; triethylamine; dicyclohexyl-carbodiimide; phosphorus trichloride; In N,N-dimethyl-formamide;

DOI:10.1248/cpb.36.3119

Reference yield:

p-aminobenzophenone (99-92-3) → {(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butyl}-carbamic acid tert-butyl ester (118792-34-0)

Guidance literature:

Multi-step reaction with 3 steps

1: 95 percent / PCl₃, pyridine / Ambient temperature

2: 25percent HBr-AcOH

3: 81 percent / HOBt, DCC, Et₃N / dimethylformamide / 4 °C

With pyridine; hydrogen bromide; benzotriazol-1-ol; acetic acid; triethylamine; dicyclohexyl-carbodiimide; phosphorus trichloride; In N,N-dimethyl-formamide;

DOI:10.1248/cpb.36.3119

upstream raw materials:

N-Boc-D-Leu

N-[(benzyloxy)carbonyl]-D-valine

p-aminobenzophenone

[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propyl]-carbamic acid benzyl ester

Downstream raw materials:

(R)-2-Amino-4-methyl-pentanoic acid [(R)-1-(4-acetyl-phenylcarbamoyl)-2-methyl-propyl]-amide; hydrochloride

N-[(S)-1-{(R)-1-[(R)-1-(4-Acetyl-phenylcarbamoyl)-2-methyl-propylcarbamoyl]-3-methyl-butylcarbamoyl}-2-(4-hydroxy-phenyl)-ethyl]-succinamic acid

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