(+/-)-methyl N-<(4-nitrophenyl)(1-pyrrolidinylcarbonyl)methyl>carbamate

Base Information

• Chemical Name: (+/-)-methyl N-<(4-nitrophenyl)(1-pyrrolidinylcarbonyl)methyl>carbamate
• CAS No.: 192188-04-8
• Molecular Formula: C₁₄H₁₇N₃O₅
• Molecular Weight: 307.306
• Mol file: 192188-04-8.mol

Synonyms:(+/-)-methyl N-<(4-nitrophenyl)(1-pyrrolidinylcarbonyl)methyl>carbamate

Chemical Property of (+/-)-methyl N-<(4-nitrophenyl)(1-pyrrolidinylcarbonyl)methyl>carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (+/-)-methyl N-<(4-nitrophenyl)(1-pyrrolidinylcarbonyl)methyl>carbamate

There total 3 articles about (+/-)-methyl N-<(4-nitrophenyl)(1-pyrrolidinylcarbonyl)methyl>carbamate 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:

2-amino-2-(4-nitrophenyl)acetic acid (5407-25-0) → (+/-)-methyl N-<(4-nitrophenyl)(1-pyrrolidinylcarbonyl)methyl>carbamate (192188-04-8)

Guidance literature:

Multi-step reaction with 3 steps

1: 86 percent / aq. NaOH / 17 h / 25 °C

2: dicyclohexylcarbodiimide / CH₂Cl₂ / 1 h

3: CH₂Cl₂ / 120 h / 25 °C

With sodium hydroxide; dicyclohexyl-carbodiimide; In dichloromethane;

DOI:10.1021/jm00052a008

Reference yield:

(+/-)-N-(methoxycarbonyl)-2-(4-nitrophenyl)glycine (192188-01-5) → (+/-)-methyl N-<(4-nitrophenyl)(1-pyrrolidinylcarbonyl)methyl>carbamate (192188-04-8)

Guidance literature:

Multi-step reaction with 2 steps

1: dicyclohexylcarbodiimide / CH₂Cl₂ / 1 h

2: CH₂Cl₂ / 120 h / 25 °C

With dicyclohexyl-carbodiimide; In dichloromethane;

DOI:10.1021/jm00052a008

Reference yield:

pyrrolidine (123-75-1) + Methoxycarbonylamino-(4-nitro-phenyl)-acetic acid benzotriazol-1-yl ester → (+/-)-methyl N-<(4-nitrophenyl)(1-pyrrolidinylcarbonyl)methyl>carbamate (192188-04-8)

Guidance literature:

In dichloromethane; at 25 ℃; for 120h; Yield given;

DOI:10.1021/jm00052a008

upstream raw materials:

pyrrolidine

2-amino-2-(4-nitrophenyl)acetic acid

(+/-)-N-(methoxycarbonyl)-2-(4-nitrophenyl)glycine

Downstream raw materials:

(+/-)-1-<2-(methylamino)-2-(4-nitrophenyl)ethyl>pyrrolidine

2-(3,4-dichlorophenyl)-N-methyl-N-<(1R,S)-1-(4-aminophenyl)-2-(1-pyrrolidinyl)ethyl>acetamide

2-(3,4-dichlorophenyl)-N-methyl-N-<(1R,S)-1-(4-nitrophenyl)-2-(1-pyrrolidinyl)ethyl>acetamide