Acetamide, N-(3-(4-bromophenyl)-1-(4-phenyl-2-thiazolyl)-1H-pyrazol-5-yl)-

Base Information

• Chemical Name: Acetamide, N-(3-(4-bromophenyl)-1-(4-phenyl-2-thiazolyl)-1H-pyrazol-5-yl)-
• CAS No.: 74101-26-1
• Molecular Formula: C₂₀H₁₅BrN₄OS
• Molecular Weight: 439.335
• DSSTox Substance ID: DTXSID90225028
• Wikidata: Q83103908
• Mol file: 74101-26-1.mol

Synonyms:BRN 1173129;Acetamide, N-(3-(4-bromophenyl)-1-(4-phenyl-2-thiazolyl)-1H-pyrazol-5-yl)-;N-(3-(4-Bromophenyl)-1-(4-phenyl-2-thiazolyl)-1H-pyrazol-5-yl)acetamide;74101-26-1;C20H15BrN4OS;DTXSID90225028;C20-H15-Br-N4-O-S;STL440177;AKOS005225092;LS-8355;N-[3-(4-bromophenyl)-1-(4-phenyl-1,3-thiazol-2-yl)-1H-pyrazol-5-yl]acetamide

Chemical Property of Acetamide, N-(3-(4-bromophenyl)-1-(4-phenyl-2-thiazolyl)-1H-pyrazol-5-yl)-

Chemical Property:

• Density: 1.52g/cm³
• XLogP3: 4.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 438.01499
• Heavy Atom Count: 27
• Complexity: 510

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)NC1=CC(=NN1C2=NC(=CS2)C3=CC=CC=C3)C4=CC=C(C=C4)Br

Technology Process of Acetamide, N-(3-(4-bromophenyl)-1-(4-phenyl-2-thiazolyl)-1H-pyrazol-5-yl)-

There total 5 articles about Acetamide, N-(3-(4-bromophenyl)-1-(4-phenyl-2-thiazolyl)-1H-pyrazol-5-yl)- 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:

2-hydrazino-4-phenylthiazole (34176-52-8) → N-[5-(4-bromo-phenyl)-2-(4-phenyl-thiazol-2-yl)-2H-pyrazol-3-yl]-acetamide (74101-26-1)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol / 0.67 h / Heating

2: Py / 3 h

With pyridine; In ethanol;

Reference yield:

α-bromoacetophenone (70-11-1) → N-[5-(4-bromo-phenyl)-2-(4-phenyl-thiazol-2-yl)-2H-pyrazol-3-yl]-acetamide (74101-26-1)

Guidance literature:

Multi-step reaction with 2 steps

1: AcOH / ethanol / 2 h / Heating

2: Py / 3 h

With pyridine; acetic acid; In ethanol;

Reference yield:

3-(4-bromophenyl)-3-oxopropanenitrile (4592-94-3) → N-[5-(4-bromo-phenyl)-2-(4-phenyl-thiazol-2-yl)-2H-pyrazol-3-yl]-acetamide (74101-26-1)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol / 0.67 h / Heating

2: Py / 3 h

With pyridine; In ethanol;

upstream raw materials:

5-(4-bromo-phenyl)-2-(4-phenyl-thiazol-2-yl)-2H-pyrazol-3-ylamine

acetic anhydride

2-hydrazino-4-phenylthiazole

α-bromoacetophenone