5-Aminopyridine-2-carboxamide

Base Information

• Chemical Name: 5-Aminopyridine-2-carboxamide
• CAS No.: 145255-19-2
• Molecular Formula: C6H7N3O
• Molecular Weight: 137.141
• Hs Code.: 2933399090
• DSSTox Substance ID: DTXSID10440251
• Wikidata: Q72441543
• Mol file: 145255-19-2.mol

Synonyms:5-aminopyridine-2-carboxamide;145255-19-2;5-aminopicolinamide;2-Pyridinecarboxamide, 5-amino-;SCHEMBL1831265;DTXSID10440251;CSHTYFRLFVBNHB-UHFFFAOYSA-N;AMY10959;MFCD09879701;AKOS006283197;CS-W022291;GS-3999;5-aminopyridine-2-carboxylic acid amide;5-Amino-pyridine-2-carboxylic acid amide;AC-23710;FT-0603745;A26265;EN300-109681;Z1116403989

Chemical Property of 5-Aminopyridine-2-carboxamide

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.644
• Boiling Point: 427.311 °C at 760 mmHg
• Flash Point: 212.23 °C
• PSA: 82.00000
• Density: 1.323 g/cm³
• LogP: 1.04420
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• XLogP3: -0.6
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 137.058911855
• Heavy Atom Count: 10
• Complexity: 137

Purity/Quality:

97% ^*data from raw suppliers

5-Aminopyridine-2-carboxamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=NC=C1N)C(=O)N
• Uses: 5-Aminopyridine-2-carboxamide is a synthetic building block used as a reactant in the discovery of carboline analogs as potent MAPKAP-K2 inhibitors.

Technology Process of 5-Aminopyridine-2-carboxamide

There total 7 articles about 5-Aminopyridine-2-carboxamide 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: 92.0%

5-amino-2-cyanopyridine (55338-73-3) → 5-aminopyridine-2-carboxylic acid amide (145255-19-2)

Guidance literature:

With dihydrogen peroxide; sodium hydroxide; In methanol; water; at 20 ℃; for 0.75h;

Reference yield: 42.0%

5-nitropyridine-2-carboxamide (59290-34-5) → 5-aminopyridine-2-carboxylic acid amide (145255-19-2)

Guidance literature:

With hydrogenchloride; iron; In ethanol; water; at 80 - 100 ℃;

Reference yield: 42.0%

→ 5-aminopyridine-2-carboxylic acid amide (145255-19-2)

Guidance literature:

With hydrogenchloride; iron; In ethanol; water; at 80 - 100 ℃;

upstream raw materials:

5-amino-2-cyanopyridine

2-bromo-5-nitropyridine

5-nitropyridine-2-carbonitrile

5-amino-pyridine-2-carboxylic acid