1-Pyrrolidinepropanamide, N-(4-nitrophenyl)-

Base Information

• Chemical Name: 1-Pyrrolidinepropanamide, N-(4-nitrophenyl)-
• CAS No.: 851651-95-1
• Molecular Formula: C13H17N3O3
• Molecular Weight: 263.296
• DSSTox Substance ID: DTXSID90469026
• Wikidata: Q82296593

Synonyms:851651-95-1;n-(4-nitrophenyl)-3-(pyrrolidin-1-yl)propanamide;1-Pyrrolidinepropanamide, N-(4-nitrophenyl)-;SCHEMBL4746764;DTXSID90469026;F96958

Chemical Property of 1-Pyrrolidinepropanamide, N-(4-nitrophenyl)-

Chemical Property:

• XLogP3: 1.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 263.12699141
• Heavy Atom Count: 19
• Complexity: 316

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN(C1)CCC(=O)NC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of 1-Pyrrolidinepropanamide, N-(4-nitrophenyl)-

There total 5 articles about 1-Pyrrolidinepropanamide, N-(4-nitrophenyl)- 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: 98.0%

pyrrolidine (123-75-1) + 3-chloro-N-(4-nitrophenyl)propanamide (19313-88-3) → N-(4-nitro-phenyl)-3-(pyrrolidin-1-yl)-propionamide (851651-95-1)

Guidance literature:

at 30 ℃;

DOI:10.1021/jm801245v

Reference yield: 97.0%

pyrrolidine (123-75-1) + 4-nitro-aniline (100-01-6,104810-17-5) + 2-chloropropionyl chloride (625-36-5) → N-(4-nitro-phenyl)-3-(pyrrolidin-1-yl)-propionamide (851651-95-1)

Guidance literature:

4-nitro-aniline; 2-chloropropionyl chloride; With triethylamine; In tetrahydrofuran; at 20 ℃; for 2.3h; Cooling with ice;

pyrrolidine; In tetrahydrofuran; at 20 ℃; for 14h; Cooling with ice;

DOI:10.1039/c0cc02917c

Reference yield: 95.0%

pyrrolidine (123-75-1) + N-(4-nitrophenyl) acrylamide (7766-38-3) → N-(4-nitro-phenyl)-3-(pyrrolidin-1-yl)-propionamide (851651-95-1)

Guidance literature:

In N,N-dimethyl-formamide; at 20 ℃; for 48h;

DOI:10.1021/jm050555a

upstream raw materials:

pyrrolidine

N-(4-nitrophenyl) acrylamide

3-chloro-N-(4-nitrophenyl)propanamide

4-nitro-aniline

Downstream raw materials:

N-(4-(4-((4-(1H-phenanthro[9,10-d]imidazol-2-yl)phenoxy)methyl)-1H-1,2,3-triazol-1-yl)phenyl)-3-(pyrrolidin-1-yl)propanamide

5,5'-ureylene-di-(1-(4-(3-(pyrrolidin-1-yl)propanamido)-phenyl)-3-phenylurea)

1,3-bis(4-(1-(4-(3-(pyrrolidin-1-yl)propanamido)phenyl)-1H-1,2,3-triazol-4-yl)phenyl)urea

1,3-bis(4-(4-(3-(pyrrolidin-1-yl)propanamido)phenylcarbamoyl)phenyl)urea

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