7-Benzoyl-5-chloroindolin-2-one

Base Information

• Chemical Name: 7-Benzoyl-5-chloroindolin-2-one
• CAS No.: 61085-27-6
• Molecular Formula: C15H10ClNO2
• Molecular Weight: 271.703
• DSSTox Substance ID: DTXSID10512563
• Wikidata: Q82371874
• Mol file: 61085-27-6.mol

Synonyms:7-Benzoyl-5-chloroindolin-2-one;61085-27-6;7-Benzoyl-5-chloro-1,3-dihydro-2H-indol-2-one;SCHEMBL11459814;DTXSID10512563;NPHJDKGTHGICQE-UHFFFAOYSA-N

Chemical Property of 7-Benzoyl-5-chloroindolin-2-one

Chemical Property:

• XLogP3: 2.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 271.0400063
• Heavy Atom Count: 19
• Complexity: 378

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C2=C(C(=CC(=C2)Cl)C(=O)C3=CC=CC=C3)NC1=O

Technology Process of 7-Benzoyl-5-chloroindolin-2-one

There total 5 articles about 7-Benzoyl-5-chloroindolin-2-one 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: 25.0%

7-Benzoyl-5-chloro-3-methylsulfanyl-1,3-dihydro-indol-2-one (91713-74-5) → 7-benzoyl-5-chloroindolin-2-one (61085-27-6)

Guidance literature:

With hydrogenchloride; tin; In ethanol; for 18h; Heating;

DOI:10.1021/jm00377a001

Reference yield:

5-chloro-2-aminobenzophenone (719-59-5) → 7-benzoyl-5-chloroindolin-2-one (61085-27-6)

Guidance literature:

Multi-step reaction with 4 steps

1: tert-butyl hypochlorite / CH₂Cl₂ / 1 h / -70 °C

2: Et₃N / CH₂Cl₂ / -70 - 20 °C

3: 3N aq. HCl / CH₂Cl₂ / 2 h / Heating

4: 25 percent / Sn, conc. aq. HCl / ethanol / 18 h / Heating

With hydrogenchloride; tin; tert-butylhypochlorite; triethylamine; In ethanol; dichloromethane;

DOI:10.1021/jm00377a001

Reference yield:

(2-Amino-3-benzoyl-5-chloro-phenyl)-methylsulfanyl-acetic acid ethyl ester → 7-benzoyl-5-chloroindolin-2-one (61085-27-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 3N aq. HCl / CH₂Cl₂ / 2 h / Heating

2: 25 percent / Sn, conc. aq. HCl / ethanol / 18 h / Heating

With hydrogenchloride; tin; In ethanol; dichloromethane;

DOI:10.1021/jm00377a001

upstream raw materials:

7-Benzoyl-5-chloro-3-methylsulfanyl-1,3-dihydro-indol-2-one

5-chloro-2-aminobenzophenone

Downstream raw materials:

2-amino-3-benzoyl-5-chlorobenzeneacetic acid, sodium salt