N-[2-(4-Bromophenyl)-2-oxoethyl]-4-pyridinecarboxamide

Base Information

Chemical Name:N-[2-(4-Bromophenyl)-2-oxoethyl]-4-pyridinecarboxamide
CAS No.:151427-14-4
Molecular Formula:C₁₄H₁₁BrN₂O₂
Molecular Weight:319.158
Hs Code.:
DSSTox Substance ID:DTXSID701210926

Synonyms:DTXSID701210926;N-[2-(4-Bromophenyl)-2-oxoethyl]-4-pyridinecarboxamide;151427-14-4

Suppliers and Price of N-[2-(4-Bromophenyl)-2-oxoethyl]-4-pyridinecarboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[2-(4-Bromophenyl)-2-oxoethyl]-4-pyridinecarboxamide

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:318.00039
Heavy Atom Count:19
Complexity:321

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)CNC(=O)C2=CC=NC=C2)Br

Technology Process of N-[2-(4-Bromophenyl)-2-oxoethyl]-4-pyridinecarboxamide

There total 3 articles about N-[2-(4-Bromophenyl)-2-oxoethyl]-4-pyridinecarboxamide 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:

: 55-22-1
pyridine-4-carboxylic acid

: 7644-04-4
4-bromophenacylamine

: 151427-14-4
N-(4'-bromophenacyl)isonicotinamide

Guidance literature:: With diisopropyl-carbodiimide; In N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(02)00999-1

Reference yield:

: 6200-09-5
(4-bromo-phenacyl)-hexamethylenetetraminium; bromide

: 151427-14-4
N-(4'-bromophenacyl)isonicotinamide

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / 48percent HBr / methanol

2: 33 percent / pyridine / 19 h

With pyridine; hydrogen bromide; In methanol;

Reference yield:

: 55-22-1
pyridine-4-carboxylic acid

: 151427-14-4
N-(4'-bromophenacyl)isonicotinamide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 0.5 h / Heating

2: 33 percent / pyridine / 19 h

With pyridine; thionyl chloride;