4a-Methoxy-7-(4-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-4-phenyl-1-phenylamino-1,4,4a,8a-tetrahydro-quinoline-5,8-dione

Base Information

• Chemical Name: 4a-Methoxy-7-(4-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-4-phenyl-1-phenylamino-1,4,4a,8a-tetrahydro-quinoline-5,8-dione
• CAS No.: 84423-27-8
• Molecular Formula: C₂₉H₂₄N₂O₆
• Molecular Weight: 496.519
• Mol file: 84423-27-8.mol

Synonyms:

Chemical Property of 4a-Methoxy-7-(4-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-4-phenyl-1-phenylamino-1,4,4a,8a-tetrahydro-quinoline-5,8-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4a-Methoxy-7-(4-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-4-phenyl-1-phenylamino-1,4,4a,8a-tetrahydro-quinoline-5,8-dione

There total 3 articles about 4a-Methoxy-7-(4-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-4-phenyl-1-phenylamino-1,4,4a,8a-tetrahydro-quinoline-5,8-dione 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: 63.0%

4,4'-Dimethoxybiphenyl-2,5,2',5'-bis-p-benzoquinone (43042-33-7) + cinnamaldehyde phenylhydrazone (1216-15-5) → 4a-Methoxy-7-(4-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-4-phenyl-1-phenylamino-1,4,4a,8a-tetrahydro-quinoline-5,8-dione (84423-27-8)

Guidance literature:

In 1,4-dioxane; for 12h; Heating;

Reference yield:

3-phenyl-propenal (104-55-2) → 4a-Methoxy-7-(4-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-4-phenyl-1-phenylamino-1,4,4a,8a-tetrahydro-quinoline-5,8-dione (84423-27-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 100 percent / piperidine / ethanol / 5 h / Heating

2: 63 percent / dioxane / 12 h / Heating

piperidine; In 1,4-dioxane; ethanol;

Reference yield:

phenylhydrazine (100-63-0) → 4a-Methoxy-7-(4-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-4-phenyl-1-phenylamino-1,4,4a,8a-tetrahydro-quinoline-5,8-dione (84423-27-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 100 percent / piperidine / ethanol / 5 h / Heating

2: 63 percent / dioxane / 12 h / Heating

piperidine; In 1,4-dioxane; ethanol;

upstream raw materials:

4,4'-Dimethoxybiphenyl-2,5,2',5'-bis-p-benzoquinone

cinnamaldehyde phenylhydrazone

3-phenyl-propenal

phenylhydrazine

Downstream raw materials:

3-Hydroxy-2,9a-dimethoxy-9-phenyl-6-phenylamino-5a,6,9,9a-tetrahydro-11-oxa-6-aza-benzo[b]fluorene-5,10-dione