2-Amino-N-(2-bromophenyl)benzamide

Base Information

• Chemical Name: 2-Amino-N-(2-bromophenyl)benzamide
• CAS No.: 34489-85-5
• Molecular Formula: C13H11 Br N2 O
• Molecular Weight: 291.147
• Hs Code.: 2924299090
• DSSTox Substance ID: DTXSID10588142
• Nikkaji Number: J3.663.089B
• Wikidata: Q72438761
• Mol file: 34489-85-5.mol

Synonyms:2-AMINO-N-(2-BROMOPHENYL)BENZAMIDE;34489-85-5;DTXSID10588142;AMY27061;AKOS000126431;DB-002423;F75318;A822254

Chemical Property of 2-Amino-N-(2-bromophenyl)benzamide

Chemical Property:

• PSA: 55.12000
• LogP: 3.93780
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 290.00548
• Heavy Atom Count: 17
• Complexity: 272

Purity/Quality:

97% ^*data from raw suppliers

Shikonofuran A ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)C(=O)NC2=CC=CC=C2Br)N

Technology Process of 2-Amino-N-(2-bromophenyl)benzamide

There total 8 articles about 2-Amino-N-(2-bromophenyl)benzamide 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: 82.0%

2-Nitro-benzoesaeure-<2-brom-anilid> (34489-84-4) → 2-amino-N-(2-bromophenyl)benzamide (34489-85-5)

Guidance literature:

With ammonium chloride; zinc; In tetrahydrofuran; water; at 20 ℃;

DOI:10.1039/c6ra00855k

Reference yield:

2-bromoaniline (615-36-1) + 2-aminobenzoyl chloride (21563-73-5) → 2-amino-N-(2-bromophenyl)benzamide (34489-85-5)

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃; for 2h;

DOI:10.1016/j.tetlet.2018.12.025

Reference yield:

2-nitrobenzyl chloride (610-14-0) → 2-amino-N-(2-bromophenyl)benzamide (34489-85-5)

Guidance literature:

Multi-step reaction with 2 steps

1: tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate / dichloromethane; water / 8 h / 20 °C / phase transfer catalysis

2: tin(ll) chloride / ethyl acetate / Reflux

With tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; tin(ll) chloride; In dichloromethane; water; ethyl acetate;

DOI:10.1055/s-0030-1260975

upstream raw materials:

isatoic anhydride

2-bromoaniline

anthranilic acid

2-Nitro-benzoesaeure-<2-brom-anilid>

Downstream raw materials:

5,10-dihydro-11H-dibenzo[b,e][1,4]-diazepin-11-one

C₁₉H₁₅BrN₂OS

2-methyl-3-(o-bromophenyl)-4(3H)-quinazolinone

3-(2-bromophenyl)benzo[d][1,2,3]triazin-4(3H)-one

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