1-[[1-[[N-(4-aminophenylsulfonyl)-N-phenylamino]acetyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

Base Information

Chemical Name:1-[[1-[[N-(4-aminophenylsulfonyl)-N-phenylamino]acetyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine
CAS No.:179173-92-3
Molecular Formula:C₂₇H₃₀N₆O₃S
Molecular Weight:518.64
Hs Code.:

Synonyms:1-[[1-[[N-(4-aminophenylsulfonyl)-N-phenylamino]acetyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

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Chemical Property of 1-[[1-[[N-(4-aminophenylsulfonyl)-N-phenylamino]acetyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

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Technology Process of 1-[[1-[[N-(4-aminophenylsulfonyl)-N-phenylamino]acetyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

There total 5 articles about 1-[[1-[[N-(4-aminophenylsulfonyl)-N-phenylamino]acetyl]-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: 78.0%

: 179173-92-3
1-[[1-[[N-(4-aminophenylsulfonyl)-N-phenylamino]acetyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

Guidance literature:

Reference yield:

: 179173-91-2
1-[[1-[[N-(4-Nitrophenylsulfonyl)-N-phenylamino]acetyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

: 179173-92-3
1-[[1-[[N-(4-aminophenylsulfonyl)-N-phenylamino]acetyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

Guidance literature:: With hydrogen; 10percent Pd/C; In methanol; for 18h;
DOI:10.1021/jm010852p

Reference yield:

: 103-01-5
N-Phenylglycine

: 179173-92-3
1-[[1-[[N-(4-aminophenylsulfonyl)-N-phenylamino]acetyl]-4-piperidyl]methyl]-1H-2-methylimidazo[4,5-c]pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 59 percent / aq. NaOH / tetrahydrofuran / 52 h

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

3: H₂ / 10percent Pd/C / methanol / 18 h

With sodium hydroxide; hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; 10percent Pd/C; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm010852p