N-(5-bromopyridin-3-yl)acetamide

Base Information

• Chemical Name: N-(5-bromopyridin-3-yl)acetamide
• CAS No.: 15862-46-1
• Molecular Formula: C7H7BrN2O
• Molecular Weight: 215.049
• Hs Code.: 2933399090
• DSSTox Substance ID: DTXSID90595238
• Nikkaji Number: J82.458E
• Wikidata: Q82490214
• Mol file: 15862-46-1.mol

Synonyms:N-(5-bromopyridin-3-yl)acetamide;15862-46-1;3-(Acetylamino)-5-bromopyridine;N-(5-Bromo-3-pyridyl)acetamide;Acetamide, N-(5-bromo-3-pyridinyl)-;MFCD13190576;856170-01-9;3-acetamido-5-bromopyridine;SCHEMBL1559057;DTXSID90595238;GZNHKIAWCLFFHP-UHFFFAOYSA-N;AMY41106;N-(5-bromo-pyridin-3-yl)-acetamide;AKOS016014387;MB13418;CS-12622;SY128013;DB-064239;CS-0061073;A850329;J-523104

Chemical Property of N-(5-bromopyridin-3-yl)acetamide

Chemical Property:

• PSA: 41.99000
• LogP: 1.87550
• Storage Temp.: Inert atmosphere,Room Temperature
• XLogP3: 0.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 213.97418
• Heavy Atom Count: 11
• Complexity: 151

Purity/Quality:

97% ^*data from raw suppliers

N-(5-Bromopyridin-3-yl)acetamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)NC1=CC(=CN=C1)Br

Technology Process of N-(5-bromopyridin-3-yl)acetamide

There total 3 articles about N-(5-bromopyridin-3-yl)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: 100.0%

3-amino-5-bromopyridine (13535-01-8) + acetyl chloride (75-36-5) → N-(5-bromo-pyridin-3-yl)-acetamide (15862-46-1)

Guidance literature:

With triethylamine;

DOI:10.1021/acsmedchemlett.6b00168

Reference yield: 97.0%

3-amino-5-bromopyridine (13535-01-8) + acetic anhydride (108-24-7) → N-(5-bromo-pyridin-3-yl)-acetamide (15862-46-1)

Guidance literature:

With pyridine; at 25 ℃; for 12h; Inert atmosphere;

Reference yield:

3,5-dibromopyridine (625-92-3) → N-(5-bromo-pyridin-3-yl)-acetamide (15862-46-1)

Guidance literature:

Multi-step reaction with 2 steps

1: CuSO₄; methanol; NH₃ / 140 °C

With methanol; ammonia; copper(II) sulfate;

upstream raw materials:

3-amino-5-bromopyridine

acetic anhydride

3,5-dibromopyridine

acetyl chloride

Downstream raw materials:

N-(5-(3-benzyl-1-(4-cyanophenyl)-3H-pyrazolo[3,4-c]quinolin-8-yl)pyridin-3-yl)acetamide

N-(5-(3-benzyl-1-bromo-3H-pyrazolo[3,4-c]quinolin-8-yl)pyridin-3-yl)acetamide

N-(5-(2-benzyl-2H-pyrazolo[3,4-c]quinolin-8-yl)pyridin-3-yl)acetamide

N-(5-(3-benzyl-3H-pyrazolo[3,4-c]quinolin-8-yl)pyridin-3-yl)acetamide