1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

Base Information

Chemical Name:1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine
CAS No.:179173-59-2
Molecular Formula:C₂₃H₂₇N₅O₃
Molecular Weight:421.499
Hs Code.:

Synonyms:1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

Suppliers and Price of 1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

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Chemical Property of 1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

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Technology Process of 1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

There total 3 articles about 1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]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: 53.0%

: 179173-59-2
1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

Guidance literature:

Reference yield:

: 6555-33-5
3(R)-(4-nitrophenyl)butanoic acid

: 173604-54-1
1-[(4-piperidyl)methyl]-1H-2-methylimidazo[4,5-c]pyridine

: 179173-59-2
1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

Guidance literature:: With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 20 ℃; for 18h;
DOI:10.1021/jm010852p

Reference yield:

: 4593-90-2,772-17-8
3-phenylbutyric acid

: 179173-59-2
1-[[1-[3-(4-Nitrophenyl)butanoyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 21 percent / HNO₃; H₂SO₄ / 1 h / 0 - 20 °C

2: HOBt; DCC / dimethylformamide / 18 h / 20 °C

With sulfuric acid; nitric acid; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide;
DOI:10.1021/jm010852p