2(1H)-Pyridinone, 3-(aMinoMethyl)-6-Methyl-4-propyl-

Base Information

• Chemical Name: 2(1H)-Pyridinone, 3-(aMinoMethyl)-6-Methyl-4-propyl-
• CAS No.: 1346575-64-1
• Molecular Formula: C10H16N2O
• Molecular Weight: 180.25
• Hs Code.: 2933399990
• Mol file: 1346575-64-1.mol

Synonyms:2(1H)-Pyridinone, 3-(aMinoMethyl)-6-Methyl-4-propyl-;3-(aMinoMethyl)-6-Methyl-4-propylpyridin-2(1H)-one acetate;3-(aminomethyl)-6-methyl-4-propyl-2(1H)-pyridinone

Chemical Property of 2(1H)-Pyridinone, 3-(aMinoMethyl)-6-Methyl-4-propyl-

Chemical Property:

• PSA: 58.88000
• LogP: 1.79480
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C

Purity/Quality:

97% ^*data from raw suppliers

3-(Aminomethyl)-6-methyl-4-propylpyridin-2(1H)-one acetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2(1H)-Pyridinone, 3-(aMinoMethyl)-6-Methyl-4-propyl-

There total 4 articles about 2(1H)-Pyridinone, 3-(aMinoMethyl)-6-Methyl-4-propyl- 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: 91.0%

1,2-dihydro-6-methyl-2-oxo-4-propylpyridine-3-carbonitrile → 3-(aminomethyl)-6-methyl-4-propyl-2(1H)-pyridinone (1346575-64-1)

Guidance literature:

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; water; at 20 ℃;

Reference yield: 60.0%

→ 3-(aminomethyl)-6-methyl-4-propyl-2(1H)-pyridinone (1346575-64-1)

Guidance literature:

Reference yield:

trans 3-hepten-2-one (5609-09-6) → 3-(aminomethyl)-6-methyl-4-propyl-2(1H)-pyridinone (1346575-64-1)

Guidance literature:

Multi-step reaction with 2 steps

1.1: potassium tert-butylate / dimethyl sulfoxide / 0.5 h / 20 °C / Inert atmosphere

1.2: 48 h / 20 °C

2.1: hydrogen; ammonia / Raney Ni / methanol / 48 h / 20 °C / 3102.97 Torr

With potassium tert-butylate; ammonia; hydrogen; Raney Ni; In methanol; dimethyl sulfoxide;

upstream raw materials:

trans 3-hepten-2-one

3-hepten-2-one

Downstream raw materials:

6-{4-[(dimethylamino)methyl]phenyl}-1-(1-methylethyl)-N-[(6-methyl-2-oxo-4-propyl-1,2-dihydro-3-pyridinyl)methyl]-1H-indazole-4-carboxamide

6-{4-[(dimethylamino)methyl]phenyl}-1-(1-methylethyl)-N-[(6-methyl-2-oxo-4-propyl-1,2-dihydro-3-pyridinyl)methyl]-1H-indazole-4-carboxamide hydrochloride

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