3-(2-cyanoethoxycarbonyl)-5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)pyridine

Base Information

• Chemical Name: 3-(2-cyanoethoxycarbonyl)-5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)pyridine
• CAS No.: 219553-54-5
• Molecular Formula: C₁₉H₂₀N₄O₅
• Molecular Weight: 384.392
• Mol file: 219553-54-5.mol

Synonyms:3-(2-cyanoethoxycarbonyl)-5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)pyridine

Chemical Property of 3-(2-cyanoethoxycarbonyl)-5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)pyridine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-(2-cyanoethoxycarbonyl)-5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)pyridine

There total 3 articles about 3-(2-cyanoethoxycarbonyl)-5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)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: 70.0%

2-cyanoethyl 3-amino-2-butenoate (88977-32-6) + N1-methyl-(Z)-2-acetyl-3-(4-nitrophenyl)-2-propenamide (219553-52-3) → 3-(2-cyanoethoxycarbonyl)-5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)pyridine (219553-54-5)

Guidance literature:

In ethanol; for 12h; Heating;

Reference yield:

N-methylacetoacetamide (20306-75-6) → 3-(2-cyanoethoxycarbonyl)-5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)pyridine (219553-54-5)

Guidance literature:

Multi-step reaction with 2 steps

1: AcOH, piperidine / propan-2-ol / 48 h / Ambient temperature

2: 70 percent / ethanol / 12 h / Heating

With piperidine; acetic acid; In ethanol; isopropyl alcohol;

Reference yield:

4-nitrobenzaldehdye (555-16-8) → 3-(2-cyanoethoxycarbonyl)-5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)pyridine (219553-54-5)

Guidance literature:

Multi-step reaction with 2 steps

1: AcOH, piperidine / propan-2-ol / 48 h / Ambient temperature

2: 70 percent / ethanol / 12 h / Heating

With piperidine; acetic acid; In ethanol; isopropyl alcohol;

upstream raw materials:

2-cyanoethyl 3-amino-2-butenoate

N₁-methyl-(Z)-2-acetyl-3-(4-nitrophenyl)-2-propenamide

N-methylacetoacetamide

4-nitrobenzaldehdye

Downstream raw materials:

5-(N-methylcarboxamido)-1,4-dihydro-2,6-dimethyl-4-(4-nitrophenyl)pyridine-3-carboxylic acid