N-(6-amino-5-iodopyridin-2-yl)acetamide

Base Information

• Chemical Name: N-(6-amino-5-iodopyridin-2-yl)acetamide
• CAS No.: 884660-45-1
• Molecular Formula: C7H8IN3O
• Molecular Weight: 277.06200
• DSSTox Substance ID: DTXSID30467763
• Wikidata: Q82294830
• Mol file: 884660-45-1.mol

Synonyms:N-(6-amino-5-iodopyridin-2-yl)acetamide;884660-45-1;N-(6-AMINO-5-IODO-(PYRIDIN-2-YL))-ACETAMIDE;tamide;SCHEMBL3056162;DTXSID30467763;AKOS004114846;n-(6-amino-5-iodo-pyridin-2-yl)-ace;N-(6-Amino-5-iodo-pyridin-2-yl)-acetamide

Chemical Property of N-(6-amino-5-iodopyridin-2-yl)acetamide

Chemical Property:

• PSA: 71.50000
• LogP: 2.45750
• XLogP3: 0.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 276.97121
• Heavy Atom Count: 12
• Complexity: 176

Purity/Quality:

99% ^*data from raw suppliers

Acetamide,N-(6-amino-5-iodo-2-pyridinyl)- 95 ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)NC1=NC(=C(C=C1)I)N

Technology Process of N-(6-amino-5-iodopyridin-2-yl)acetamide

There total 2 articles about N-(6-amino-5-iodopyridin-2-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: 85.0%

2,6-diamino-3-iodopyridine (856851-34-8) + acetic anhydride (108-24-7) → N-(6-amino-5-iodopyridin-2-yl)acetamide (884660-45-1)

Guidance literature:

With pyridine; at 20 ℃; for 12h;

DOI:10.1021/jo060066y

Reference yield:

2.6-diaminopyridine (141-86-6) → N-(6-amino-5-iodopyridin-2-yl)acetamide (884660-45-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 60 percent / AcOH; H₂SO₄; I₂ / periodic acid / H₂O / 5 h / 55 °C

2: 85 percent / pyridine / 12 h / 20 °C

With pyridine; sulfuric acid; iodine; acetic acid; periodic acid; In water;

DOI:10.1021/jo060066y

Reference yield: 64.0%

N-(6-amino-5-iodopyridin-2-yl)acetamide (884660-45-1) → N-(6-fluoro-5-iodopyridin-2-yl)acetamide (884660-46-2)

Guidance literature:

With tetrafluoroboric acid; sodium nitrite; In water; at -5 ℃; for 2h;

DOI:10.1021/jo060066y

upstream raw materials:

2,6-diamino-3-iodopyridine

acetic anhydride

2.6-diaminopyridine

Downstream raw materials:

N-(6-fluoro-5-iodopyridin-2-yl)acetamide

6-amino-2-fluoro-3-iodopyridine

2-fluoro-6-hydroxy-3-iodopyridine

6-(2-(4-nitrophenyl)ethoxy)-2-fluoro-3-iodopyridine