(4,6-Dimethylpyridin-2-YL)methanamine

Base Information

• Chemical Name: (4,6-Dimethylpyridin-2-YL)methanamine
• CAS No.: 76457-15-3
• Molecular Formula: C8H12N2
• Molecular Weight: 136.197
• European Community (EC) Number: 867-032-2
• Nikkaji Number: J2.806.776C
• Mol file: 76457-15-3.mol

Synonyms:(4,6-DIMETHYLPYRIDIN-2-YL)METHANAMINE;76457-15-3;SCHEMBL943293;MFCD10700198;AKOS006304884;AB62613;CS-0216291;EN300-384700;1-(4,6-DIMETHYLPYRIDIN-2-YL)METHANAMINE;J-501341;F2147-2305

Chemical Property of (4,6-Dimethylpyridin-2-YL)methanamine

Chemical Property:

• PSA: 38.91000
• LogP: 1.85740
• XLogP3: 0.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 136.100048391
• Heavy Atom Count: 10
• Complexity: 103

Purity/Quality:

99% ^*data from raw suppliers

(4,6-dimethylpyridin-2-yl)methanamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=NC(=C1)CN)C

Technology Process of (4,6-Dimethylpyridin-2-YL)methanamine

There total 3 articles about (4,6-Dimethylpyridin-2-YL)methanamine 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: 98.0%

4,6-dimethylpyridine-2-carbonitrile (7584-11-4) → 1-(4,6-dimethylpyridin-2-yl)methanamine (76457-15-3)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; at 0 ℃; for 0.05h;

DOI:10.1002/jhet.5570170541

Reference yield:

2,4-dimethylpyridine N-oxide (1122-45-8) → 1-(4,6-dimethylpyridin-2-yl)methanamine (76457-15-3)

Guidance literature:

Multi-step reaction with 2 steps

1.1: dichloromethane / 0.25 h / 20 °C

1.2: 20 h / 20 °C

2.1: palladium 10% on activated carbon; hydrogen / ethanol / 16 h

With palladium 10% on activated carbon; hydrogen; In ethanol; dichloromethane;

Reference yield:

2,4-lutidine (108-47-4) → 1-(4,6-dimethylpyridin-2-yl)methanamine (76457-15-3)

Guidance literature:

Multi-step reaction with 3 steps

1.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 16 h / 20 °C / Cooling with ice

2.1: dichloromethane / 0.25 h / 20 °C

2.2: 20 h / 20 °C

3.1: palladium 10% on activated carbon; hydrogen / ethanol / 16 h

With palladium 10% on activated carbon; hydrogen; 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane;

upstream raw materials:

4,6-dimethylpyridine-2-carbonitrile

2,4-dimethylpyridine N-oxide

2,4-lutidine

Refernces

• 1、 -. "COMPOUNDS AND THEIR USE AS PDE4 ACTIVATORS". Page/Page column 86-87. . Retrieved 2019/10/29.