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

Base Information

• Chemical Name: 2-(3,4-dichlorophenyl)-N-methyl-N-<(1R,S)-1-(4-aminophenyl)-2-(1-pyrrolidinyl)ethyl>acetamide
• CAS No.: 130109-60-3
• Molecular Formula: C₂₁H₂₅Cl₂N₃O
• Molecular Weight: 406.355
• Mol file: 130109-60-3.mol

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

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

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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

There total 8 articles about 2-(3,4-dichlorophenyl)-N-methyl-N-<(1R,S)-1-(4-aminophenyl)-2-(1-pyrrolidinyl)ethyl>acetamide 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: 59.0%

2-(3,4-dichlorophenyl)-N-methyl-N-<(1R,S)-1-(4-nitrophenyl)-2-(1-pyrrolidinyl)ethyl>acetamide (130109-48-7) → 2-(3,4-dichlorophenyl)-N-methyl-N-<(1R,S)-1-(4-aminophenyl)-2-(1-pyrrolidinyl)ethyl>acetamide (130109-60-3)

Guidance literature:

With hydrazine; nickel; In ethanol; at 55 ℃; for 2.5h;

DOI:10.1021/jm00052a008

Reference yield:

3,4-dichlorophenyl acetic acid (5807-30-7) → 2-(3,4-dichlorophenyl)-N-methyl-N-<(1R,S)-1-(4-aminophenyl)-2-(1-pyrrolidinyl)ethyl>acetamide (130109-60-3)

Guidance literature:

Multi-step reaction with 3 steps

1: thionyl chloride / 2.5 h / 76 °C

2: Et₃N / CH₂Cl₂ / 21 h / 25 °C

3: 59 percent / hydrazine / Raney Ni / aq. ethanol / 2.5 h / 55 °C

With thionyl chloride; triethylamine; hydrazine; nickel; In ethanol; dichloromethane;

DOI:10.1021/jm00052a008

Reference yield:

2-amino-2-(4-nitrophenyl)acetic acid (5407-25-0) → 2-(3,4-dichlorophenyl)-N-methyl-N-<(1R,S)-1-(4-aminophenyl)-2-(1-pyrrolidinyl)ethyl>acetamide (130109-60-3)

Guidance literature:

Multi-step reaction with 6 steps

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

2: dicyclohexylcarbodiimide / CH₂Cl₂ / 1 h

3: CH₂Cl₂ / 120 h / 25 °C

4: 49.7 percent / BH₃*THF / tetrahydrofuran / 96 h / Heating

5: Et₃N / CH₂Cl₂ / 21 h / 25 °C

6: 59 percent / hydrazine / Raney Ni / aq. ethanol / 2.5 h / 55 °C

With sodium hydroxide; borane-THF; triethylamine; dicyclohexyl-carbodiimide; hydrazine; nickel; In tetrahydrofuran; ethanol; dichloromethane;

DOI:10.1021/jm00052a008

upstream raw materials:

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

3,4-dichlorophenyl acetic acid

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

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