2-amino-5-(4-bromo-phenyl)-1-phenyl-1H-pyrrole-3-carbonitrile

Base Information

• Chemical Name: 2-amino-5-(4-bromo-phenyl)-1-phenyl-1H-pyrrole-3-carbonitrile
• CAS No.: 748810-19-7
• Molecular Formula: C₁₇H₁₂BrN₃
• Molecular Weight: 338.206
• Mol file: 748810-19-7.mol

Synonyms:2-amino-5-(4-bromo-phenyl)-1-phenyl-1H-pyrrole-3-carbonitrile

Chemical Property of 2-amino-5-(4-bromo-phenyl)-1-phenyl-1H-pyrrole-3-carbonitrile

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-amino-5-(4-bromo-phenyl)-1-phenyl-1H-pyrrole-3-carbonitrile

There total 2 articles about 2-amino-5-(4-bromo-phenyl)-1-phenyl-1H-pyrrole-3-carbonitrile 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: 39.0%

2,2-bis[2-(4-chlorophenyl)-2-oxoethyl]propanedinitrile (26454-82-0) + aniline (62-53-3) → 2-amino-5-(4-bromo-phenyl)-1-phenyl-1H-pyrrole-3-carbonitrile (748810-19-7)

Guidance literature:

With hydrogenchloride; In ethanol; for 120h; Heating;

DOI:10.1002/ardp.200300773

Reference yield:

para-bromophenacyl bromide (99-73-0,132309-76-3) → 2-amino-5-(4-bromo-phenyl)-1-phenyl-1H-pyrrole-3-carbonitrile (748810-19-7)

Guidance literature:

Multi-step reaction with 2 steps

1: NaOH / ethanol; H₂O

2: 39 percent / conc. HCl / ethanol / 120 h / Heating

With hydrogenchloride; sodium hydroxide; In ethanol; water;

DOI:10.1002/ardp.200300773

Reference yield: 96.0%

orthoformic acid triethyl ester (122-51-0) + 2-amino-5-(4-bromo-phenyl)-1-phenyl-1H-pyrrole-3-carbonitrile (748810-19-7) → N-[5-(4-bromo-phenyl)-3-cyano-1-phenyl-1H-pyrrol-2-yl]formimidic acid ethyl ester (1257391-46-0)

Guidance literature:

for 4h; Reflux;

DOI:10.1016/j.ejmech.2010.08.043

upstream raw materials:

2,2-bis[2-(4-chlorophenyl)-2-oxoethyl]propanedinitrile

aniline

para-bromophenacyl bromide

Downstream raw materials:

6-(4-bromophenyl)-7-phenyl-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one

N-[5-(4-bromo-phenyl)-3-cyano-1-phenyl-1H-pyrrol-2-yl]formimidic acid ethyl ester

6-(4-bromophenyl)-2-(ethylthio)-7-phenylpyrrolo[2,3-d][1,3]thiazin-4(7H)-imine

6-(4-bromophenyl)-7-phenyl-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dithione