1-Methylimidazo[1,5-a]pyridine

Base Information

• Chemical Name: 1-Methylimidazo[1,5-a]pyridine
• CAS No.: 6558-62-9
• Molecular Formula: C₈H₈N₂
• Molecular Weight: 132.165
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID30378022
• Nikkaji Number: J948.657G
• Wikidata: Q82167457
• Mol file: 6558-62-9.mol

Synonyms:1-methylimidazo[1,5-a]pyridine;6558-62-9;1-METHYL-IMIDAZO[1,5-A]PYRIDINE;Imidazo[1,5-a]pyridine,1-methyl-;MFCD06245386;SCHEMBL9934394;DTXSID30378022;AKOS005257458;PS-3053;2-Isopropyl-4-methyl-pyrimidine-5-carboxylicacid

Chemical Property of 1-Methylimidazo[1,5-a]pyridine

Chemical Property:

• PSA: 17.30000
• Density: 1.11g/cm³
• LogP: 1.64270
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 132.068748264
• Heavy Atom Count: 10
• Complexity: 124

Purity/Quality:

99% ^*data from raw suppliers

1-Methylimidazo[1,5-a]pyridine ^*data from reagent suppliers

Safty Information:

• Hazard Codes: T

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C2C=CC=CN2C=N1

Technology Process of 1-Methylimidazo[1,5-a]pyridine

There total 3 articles about 1-Methylimidazo[1,5-a]pyridine 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: 87.0%

N-[((1-pyridin-2-yl)ethyl)]formamide (854701-06-7) → 1-methylimidazo[1,5-a]pyridine (6558-62-9)

Guidance literature:

With trichlorophosphate; In toluene; at 20 - 100 ℃; Inert atmosphere;

Reference yield:

2-acetylpyridine (1122-62-9) → 1-methylimidazo[1,5-a]pyridine (6558-62-9)

Guidance literature:

Multi-step reaction with 3 steps

1.1: hydroxylamine hydrochloride; potassium carbonate / methanol / 4 h / 20 °C

1.2: 20 °C

2.1: 0 - 100 °C

3.1: trichlorophosphate / toluene / 20 - 100 °C / Inert atmosphere

With hydroxylamine hydrochloride; potassium carbonate; trichlorophosphate; In methanol; toluene;

Reference yield:

2-aminoethylpyridine (42088-91-5) → 1-methylimidazo[1,5-a]pyridine (6558-62-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 0 - 100 °C

2: trichlorophosphate / toluene / 20 - 100 °C / Inert atmosphere

With trichlorophosphate; In toluene;

upstream raw materials:

N-[((1-pyridin-2-yl)ethyl)]formamide

2-acetylpyridine

2-aminoethylpyridine