7-Chloro-1-(4-methoxy-phenyl)-4-methyl-9-phenyl-4,10a-dihydro-1H-2-oxa-3,4,10-triaza-benzo[f]azulene

Base Information

• Chemical Name: 7-Chloro-1-(4-methoxy-phenyl)-4-methyl-9-phenyl-4,10a-dihydro-1H-2-oxa-3,4,10-triaza-benzo[f]azulene
• CAS No.: 142427-79-0
• Molecular Formula: C₂₄H₂₀ClN₃O₂
• Molecular Weight: 417.895

Synonyms:7-Chloro-1-(4-methoxy-phenyl)-4-methyl-9-phenyl-4,10a-dihydro-1H-2-oxa-3,4,10-triaza-benzo[f]azulene

Chemical Property of 7-Chloro-1-(4-methoxy-phenyl)-4-methyl-9-phenyl-4,10a-dihydro-1H-2-oxa-3,4,10-triaza-benzo[f]azulene

Chemical Property:

Purity/Quality:

98% ^*data from raw suppliers

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Technology Process of 7-Chloro-1-(4-methoxy-phenyl)-4-methyl-9-phenyl-4,10a-dihydro-1H-2-oxa-3,4,10-triaza-benzo[f]azulene

There total 3 articles about 7-Chloro-1-(4-methoxy-phenyl)-4-methyl-9-phenyl-4,10a-dihydro-1H-2-oxa-3,4,10-triaza-benzo[f]azulene 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: 60.0%

7-Chloro-3-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-1-methyl-5-phenyl-1,3-dihydro-benzo[e][1,4]diazepin-2-one (142427-86-9) → 7-Chloro-1-(4-methoxy-phenyl)-4-methyl-9-phenyl-4,10a-dihydro-1H-2-oxa-3,4,10-triaza-benzo[f]azulene (142427-79-0)

Guidance literature:

With sodium hydroxide; hydroxylamine; In methanol; for 3h; Heating;

DOI:10.1002/ardp.19923250507

Reference yield:

4-methoxy-benzaldehyde (123-11-5) → 7-Chloro-1-(4-methoxy-phenyl)-4-methyl-9-phenyl-4,10a-dihydro-1H-2-oxa-3,4,10-triaza-benzo[f]azulene (142427-79-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 75 percent / 4percent ethanolic KOH / 3 h / Heating

2: 60 percent / aq. NH₂OH, aq. NaOH / methanol / 3 h / Heating

With potassium hydroxide; sodium hydroxide; hydroxylamine; In methanol;

DOI:10.1002/ardp.19923250507

Reference yield:

diazepam (439-14-5) → 7-Chloro-1-(4-methoxy-phenyl)-4-methyl-9-phenyl-4,10a-dihydro-1H-2-oxa-3,4,10-triaza-benzo[f]azulene (142427-79-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 75 percent / 4percent ethanolic KOH / 3 h / Heating

2: 60 percent / aq. NH₂OH, aq. NaOH / methanol / 3 h / Heating

With potassium hydroxide; sodium hydroxide; hydroxylamine; In methanol;

DOI:10.1002/ardp.19923250507

upstream raw materials:

7-Chloro-3-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-1-methyl-5-phenyl-1,3-dihydro-benzo[e][1,4]diazepin-2-one

4-methoxy-benzaldehyde

diazepam

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