2-Amino-6-(1-piperidinyl)benzonitrile

Base Information

• Chemical Name: 2-Amino-6-(1-piperidinyl)benzonitrile
• CAS No.: 63365-14-0
• Molecular Formula: C12H15N3
• Molecular Weight: 201.271
• DSSTox Substance ID: DTXSID00507802
• Mol file: 63365-14-0.mol

Synonyms:63365-14-0;2-amino-6-(1-piperidinyl)benzonitrile;SCHEMBL533684;2-amino-6-piperidinobenzonitrile;DTXSID00507802;NJGCGPLXNSRJFG-UHFFFAOYSA-N;2-Amino-6-(1-piperdinyl)benzonitrile;2-(1-piperidinyl)-6-aminobenzonitrile;2-amino-6-(1-piperidinyl)-benzonitrile;2-Amino-6-(piperidin-1-yl)benzonitrile

Chemical Property of 2-Amino-6-(1-piperidinyl)benzonitrile

Chemical Property:

• XLogP3: 2.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 201.126597491
• Heavy Atom Count: 15
• Complexity: 249

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN(CC1)C2=CC=CC(=C2C#N)N

Technology Process of 2-Amino-6-(1-piperidinyl)benzonitrile

There total 5 articles about 2-Amino-6-(1-piperidinyl)benzonitrile 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: 64.0%

2-nitro-6-(1-piperidinyl)benzonitrile (63365-13-9) → 2-amino-6-(1-piperidinyl)benzonitrile (63365-14-0)

Guidance literature:

With cyclohexene; palladium on activated charcoal; In ethanol; for 0.25h; Heating;

DOI:10.1021/jm00138a020

Reference yield:

2,6-dinitrobenzonitrile (35213-00-4) → 2-amino-6-(1-piperidinyl)benzonitrile (63365-14-0)

Guidance literature:

Multi-step reaction with 2 steps

1: dimethylformamide / 0.5 h / 50 °C

2: conc. aq. HCl, SnCl₂*2H₂O / 2 h / Ambient temperature

With hydrogenchloride; tin(ll) chloride; In N,N-dimethyl-formamide;

DOI:10.1021/jm00148a003

Reference yield:

piperidine (110-89-4) → 2-amino-6-(1-piperidinyl)benzonitrile (63365-14-0)

Guidance literature:

Multi-step reaction with 2 steps

1: dimethylformamide / 0.5 h / 50 °C

2: conc. aq. HCl, SnCl₂*2H₂O / 2 h / Ambient temperature

With hydrogenchloride; tin(ll) chloride; In N,N-dimethyl-formamide;

DOI:10.1021/jm00148a003

upstream raw materials:

2-nitro-6-(1-piperidinyl)benzonitrile

piperidine

2,6-dinitrobenzonitrile

2-amino-6-fluorobenzonitrile

Downstream raw materials:

N-[2-cyano-3-(1-piperidinyl)phenyl]1-(4-methoxyphenylmethyl)-1H-tetrazole-5-carboxamide

[2-Cyano-3-(1-Piperidinyl)Phenylamino]Oxoacetic Acid Ethyl Ester

[3-Amino-2-Cyanophenylamino]Oxoacetic Acid Ethyl Ester

2-Amino-6-piperidin-1-yl-benzylamine