N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

Base Information

Chemical Name:N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide
CAS No.:104374-00-7
Molecular Formula:C₂₀H₂₅N₇O₃
Molecular Weight:411.464
Hs Code.:

Synonyms:N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

Suppliers and Price of N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

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Technology Process of N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

There total 4 articles about N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide 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: 16.0%

: potassium cyanate

: 86523-76-4
N-(4-aminophenyl)-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

: 86523-79-7
N-<4-<(aminocarbonyl)amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

: 104374-00-7
N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

Guidance literature:: With hydrogenchloride; for 8h;
DOI:10.1021/jm00384a002

Reference yield:

: 34803-66-2
1-(2-pyridyl)piperazine

: 104374-00-7
N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

Guidance literature:: Multi-step reaction with 3 steps

1: 69 percent / benzene / Heating

2: 73 percent / H₂ / 10percent Pd/C / methanol / 3102.9 Torr

3: 3 percent / 1 N aq. HCl / 8 h

With hydrogenchloride; hydrogen; palladium on activated charcoal; In methanol; benzene;
DOI:10.1021/jm00384a002

Reference yield:

: 7766-38-3
N-(4-nitrophenyl) acrylamide

: 104374-00-7
N-<4-<<<(aminocarbonyl)amino>carbonyl>amino>phenyl>-3-<4-(2-pyridinyl)-1-piperazinyl>propanamide

Guidance literature:: Multi-step reaction with 3 steps

1: 69 percent / benzene / Heating

2: 73 percent / H₂ / 10percent Pd/C / methanol / 3102.9 Torr

3: 3 percent / 1 N aq. HCl / 8 h

With hydrogenchloride; hydrogen; palladium on activated charcoal; In methanol; benzene;
DOI:10.1021/jm00384a002