N-[4-(2-nitrobenzenesulfonyl)aminobutan-1-yl]-1H-indole-3-acetamide

Base Information

• Chemical Name: N-[4-(2-nitrobenzenesulfonyl)aminobutan-1-yl]-1H-indole-3-acetamide
• CAS No.: 240423-14-7
• Molecular Formula: C₂₀H₂₂N₄O₅S
• Molecular Weight: 430.484
• Mol file: 240423-14-7.mol

Synonyms:N-[4-(2-nitrobenzenesulfonyl)aminobutan-1-yl]-1H-indole-3-acetamide

Chemical Property of N-[4-(2-nitrobenzenesulfonyl)aminobutan-1-yl]-1H-indole-3-acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-[4-(2-nitrobenzenesulfonyl)aminobutan-1-yl]-1H-indole-3-acetamide

There total 4 articles about N-[4-(2-nitrobenzenesulfonyl)aminobutan-1-yl]-1H-indole-3-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: 97.0%

C15H17NO3 (125213-31-2) + N-(4-aminobutan-1-yl)-2-nitrobenzenesulfonamide (211512-13-9) → N-[4-(2-nitrobenzenesulfonyl)aminobutan-1-yl]-1H-indole-3-acetamide (240423-14-7)

Guidance literature:

With dmap; triethylamine; In dichloromethane;

DOI:10.1016/S0040-4039(99)00851-5

Reference yield:

2-Nitrobenzenesulfonyl chloride (1694-92-4) → N-[4-(2-nitrobenzenesulfonyl)aminobutan-1-yl]-1H-indole-3-acetamide (240423-14-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 77 percent / ethanol / 0.5 h

2: Et₃N; DMAP / CH₂Cl₂ / 0.17 h / 20 °C

With dmap; triethylamine; In ethanol; dichloromethane;

DOI:10.1248/cpb.48.1570

Reference yield:

indole-3-acetic acid (87-51-4) → N-[4-(2-nitrobenzenesulfonyl)aminobutan-1-yl]-1H-indole-3-acetamide (240423-14-7)

Guidance literature:

Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 20 °C

2: 97 percent / Et₃N; DMAP / CH₂Cl₂

With dmap; triethylamine; In dichloromethane; 1: Acylation / 2: Condensation;

DOI:10.1016/S0040-4039(99)00851-5

upstream raw materials:

C₁₅H₁₇NO₃

N-(4-aminobutan-1-yl)-2-nitrobenzenesulfonamide

indole-3-acetic acid

2-Nitrobenzenesulfonyl chloride

Downstream raw materials:

N-[16-amino-5,9,13-tris(2-nitrobenzenesulfonyl)-5,9,13-triazahexadecan-1-yl]-1H-indole-3-acetamide

HO 416b

N-[16-tert-butoxycarbonylamino-5,9,13-tris(2-nitrobenzenesulfonyl)-5,9,13-triazahexadecan-1-yl]-1H-indole-3-acetamide