4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid

Base Information

• Chemical Name: 4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid
• CAS No.: 132026-12-1
• Molecular Formula: C14H11N3O2
• Molecular Weight: 253.26
• DSSTox Substance ID: DTXSID30440415
• Nikkaji Number: J694.022F
• Wikidata: Q82256720
• Mol file: 132026-12-1.mol

Synonyms:4-(2-METHYL-1H-IMIDAZO[4,5-C]PYRIDIN-1-YL)BENZOIC ACID;132026-12-1;4-(2-methylimidazo[4,5-c]pyridin-1-yl)benzoic acid;4-{2-methyl-1H-imidazo[4,5-c]pyridin-1-yl}benzoic acid;4-(2-methylimidazo[4,5-c]pyridinyl)benzoic acid;SCHEMBL7505146;DTXSID30440415;ZPSBZAONUUOSTH-UHFFFAOYSA-N;4-(2-Methylimidazo[4,5-c]pyrid-1-yl)benzoic acid

Chemical Property of 4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid

Chemical Property:

• PSA: 68.01000
• LogP: 2.42710
• XLogP3: 2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 253.085126602
• Heavy Atom Count: 19
• Complexity: 342

Purity/Quality:

97% ^*data from raw suppliers

4-(2-METHYL-1H-IMIDAZO-[4,5-C]-PYRIDIN-1-YL)BENZOIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1=NC2=C(N1C3=CC=C(C=C3)C(=O)O)C=CN=C2

Technology Process of 4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid

There total 1 articles about 4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid 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: 70.0%

4-(2-methylimidazo[4,5-c]pyrid-1-yl)benzonitrile (122957-32-8) → 4-(1H-2-methylimidazo[4,5-c]pyridin-1-yl)benzoic acid (132026-12-1)

Guidance literature:

With sodium hydroxide; In ice-water; ethanol; water; acetic acid;

Reference yield: 23.0%

oxalyl dichloride (79-37-8) + L-leucine ethyl ester hydrochloride (2743-40-0) + 4-(1H-2-methylimidazo[4,5-c]pyridin-1-yl)benzoic acid (132026-12-1) → N-4-(2-methylimidazo[4,5-c]pyridin-1-yl)benzoyl-L-leucine ethyl ester

Guidance literature:

With triethylamine; In methanol; 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

4-(1H-2-methylimidazo[4,5-c]pyridin-1-yl)benzoic acid (132026-12-1) → 4-(2-Methyl-imidazo[4,5-c]pyridin-1-yl)-benzoyl chloride (132504-92-8)

Guidance literature:

With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20 ℃; for 1h;

DOI:10.1021/jm00018a011

upstream raw materials:

4-(2-methylimidazo[4,5-c]pyrid-1-yl)benzonitrile

Downstream raw materials:

4-(2-Methyl-imidazo[4,5-c]pyridin-1-yl)-benzoyl chloride

N-benzoyl-N'-<4-(2-methylimidazo<4,5-c>pyrid-1-yl)benzoyl>hydrazine

ethyl 4'-(2-methylimidazo[4,5-c]pyridin-1-yl)benzoylacetate

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