2H-Indol-2-one, 1,3-dihydro-5-methyl-1-(4-methylphenyl)-3-(phenylthio)-

Base Information

• Chemical Name: 2H-Indol-2-one, 1,3-dihydro-5-methyl-1-(4-methylphenyl)-3-(phenylthio)-
• CAS No.: 193815-37-1
• Molecular Formula: C22H19NOS
• Molecular Weight: 345.465
• DSSTox Substance ID: DTXSID90472934
• Nikkaji Number: J876.542A

Synonyms:193815-37-1;2H-Indol-2-one, 1,3-dihydro-5-methyl-1-(4-methylphenyl)-3-(phenylthio)-;DTXSID90472934

Chemical Property of 2H-Indol-2-one, 1,3-dihydro-5-methyl-1-(4-methylphenyl)-3-(phenylthio)-

Chemical Property:

• XLogP3: 5.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 345.11873540
• Heavy Atom Count: 25
• Complexity: 467

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)N2C3=C(C=C(C=C3)C)C(C2=O)SC4=CC=CC=C4

Technology Process of 2H-Indol-2-one, 1,3-dihydro-5-methyl-1-(4-methylphenyl)-3-(phenylthio)-

There total 4 articles about 2H-Indol-2-one, 1,3-dihydro-5-methyl-1-(4-methylphenyl)-3-(phenylthio)- 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:

2-Benzenesulfinyl-N,N-di-p-tolyl-acetamide (1027076-88-5) → 5-Methyl-3-phenylsulfanyl-1-p-tolyl-1,3-dihydro-indol-2-one (193815-37-1)

Guidance literature:

With toluene-4-sulfonic acid; In tetrachloromethane; Heating;

DOI:10.1021/jo971173i

Reference yield:

(phenylthio)acetic acid chloride (7031-27-8) → 5-Methyl-3-phenylsulfanyl-1-p-tolyl-1,3-dihydro-indol-2-one (193815-37-1)

Guidance literature:

Multi-step reaction with 3 steps

2: mCPBA

3: p-TosOH / CCl₄ / Heating

With toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; In tetrachloromethane;

DOI:10.1021/jo971173i

Reference yield:

di-p-tolylamine (620-93-9) → 5-Methyl-3-phenylsulfanyl-1-p-tolyl-1,3-dihydro-indol-2-one (193815-37-1)

Guidance literature:

Multi-step reaction with 3 steps

2: mCPBA

3: p-TosOH / CCl₄ / Heating

With toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; In tetrachloromethane;

DOI:10.1021/jo971173i

upstream raw materials:

2-Benzenesulfinyl-N,N-di-p-tolyl-acetamide

(phenylthio)acetic acid chloride

di-p-tolylamine

2-Phenylsulfanyl-N,N-di-p-tolyl-acetamide

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