3-nitro-N-propylpyridin-2-amine

Base Information

• Chemical Name: 3-nitro-N-propylpyridin-2-amine
• CAS No.: 26820-66-6
• Molecular Formula: C8H11N3O2
• DSSTox Substance ID: DTXSID601303213
• Mol file: 26820-66-6.mol

Synonyms:3-nitro-N-propylpyridin-2-amine;26820-66-6;3-nitro-N-propyl-2-pyridinamine;MFCD08692147;2-Pyridinamine, 3-nitro-N-propyl-;SCHEMBL14099477;DTXSID601303213;BBA82066;AKOS001878217;SB53906;BS-38853;DB-010130

Chemical Property of 3-nitro-N-propylpyridin-2-amine

Chemical Property:

• Vapor Pressure: 0.000575mmHg at 25°C
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 181.085126602
• Heavy Atom Count: 13
• Complexity: 169

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCNC1=C(C=CC=N1)[N+](=O)[O-]

Technology Process of 3-nitro-N-propylpyridin-2-amine

There total 2 articles about 3-nitro-N-propylpyridin-2-amine 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:

propylamine (107-10-8,42939-71-9) + 2-Chloro-3-nitropyridine (5470-18-8,34515-82-7) → 2-propylamino-3-nitropyridine (26820-66-6)

Guidance literature:

In acetonitrile; at 20 ℃; for 5h;

Reference yield:

→ 2-propylamino-3-nitropyridine (26820-66-6)

Guidance literature:

entspr. Hydroxypyridin, entspr. NH2-Verb., Subst.;

Reference yield:

2-propylamino-3-nitropyridine (26820-66-6) → 1-propyl-2-(4-methoxybenzylamino)methyl-7-azabenzimidazole (439571-82-1)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrogen / palladium 10% on activated carbon / ethanol; ethyl acetate / 2068.65 Torr

2: potassium carbonate / chloroform / 3 h / 20 °C

3: acetonitrile / 10 h / 20 °C

With hydrogen; potassium carbonate; palladium 10% on activated carbon; In ethanol; chloroform; ethyl acetate; acetonitrile;

upstream raw materials:

propylamine

2-Chloro-3-nitropyridine

Downstream raw materials:

N²-propyl-pyridine-2,3-diyldiamine

1-propyl-2-chloromethyl-7-azabenzimidazole

1-propyl-2-(4-methoxybenzylamino)methyl-7-azabenzimidazole

N-(4-methoxy-benzyl)-N-(3-propyl-3H-imidazo[4,5-b]pyridin-2-ylmethyl)-benzamide