2-Chloro-10-(4-methoxy-phenyl)-5-methyl-12-phenyl-5,9,10,10a-tetrahydro-7H-5,6,7,9,11-pentaaza-benzo[b]heptalene-8-thione

Base Information

• Chemical Name: 2-Chloro-10-(4-methoxy-phenyl)-5-methyl-12-phenyl-5,9,10,10a-tetrahydro-7H-5,6,7,9,11-pentaaza-benzo[b]heptalene-8-thione
• CAS No.: 142427-85-8
• Molecular Formula: C₂₅H₂₂ClN₅OS
• Molecular Weight: 476.002
• Mol file: 142427-85-8.mol

Synonyms:

Chemical Property of 2-Chloro-10-(4-methoxy-phenyl)-5-methyl-12-phenyl-5,9,10,10a-tetrahydro-7H-5,6,7,9,11-pentaaza-benzo[b]heptalene-8-thione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-Chloro-10-(4-methoxy-phenyl)-5-methyl-12-phenyl-5,9,10,10a-tetrahydro-7H-5,6,7,9,11-pentaaza-benzo[b]heptalene-8-thione

There total 3 articles about 2-Chloro-10-(4-methoxy-phenyl)-5-methyl-12-phenyl-5,9,10,10a-tetrahydro-7H-5,6,7,9,11-pentaaza-benzo[b]heptalene-8-thione 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: 30.0%

thiosemicarbazide (79-19-6) + 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) → 2-Chloro-10-(4-methoxy-phenyl)-5-methyl-12-phenyl-5,9,10,10a-tetrahydro-7H-5,6,7,9,11-pentaaza-benzo[b]heptalene-8-thione (142427-85-8)

Guidance literature:

With potassium hydroxide; In ethanol; for 4h; Heating;

DOI:10.1002/ardp.19923250507

Reference yield:

4-methoxy-benzaldehyde (123-11-5) → 2-Chloro-10-(4-methoxy-phenyl)-5-methyl-12-phenyl-5,9,10,10a-tetrahydro-7H-5,6,7,9,11-pentaaza-benzo[b]heptalene-8-thione (142427-85-8)

Guidance literature:

Multi-step reaction with 2 steps

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

2: 30 percent / aq. KOH / ethanol / 4 h / Heating

With potassium hydroxide; In ethanol;

DOI:10.1002/ardp.19923250507

Reference yield:

diazepam (439-14-5) → 2-Chloro-10-(4-methoxy-phenyl)-5-methyl-12-phenyl-5,9,10,10a-tetrahydro-7H-5,6,7,9,11-pentaaza-benzo[b]heptalene-8-thione (142427-85-8)

Guidance literature:

Multi-step reaction with 2 steps

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

2: 30 percent / aq. KOH / ethanol / 4 h / Heating

With potassium hydroxide; In ethanol;

DOI:10.1002/ardp.19923250507

upstream raw materials:

thiosemicarbazide

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