1H-Indol-1-acetic acid, 2,3-dihydro-3,3-diphenyl-2-oxo-5-(((2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)amino)carbonyl)-

Base Information

Chemical Name:1H-Indol-1-acetic acid, 2,3-dihydro-3,3-diphenyl-2-oxo-5-(((2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)amino)carbonyl)-
CAS No.:100549-95-9
Molecular Formula:C34H28 N4 O5
Molecular Weight:0
Hs Code.:
DSSTox Substance ID:DTXSID70143377
Wikidata:Q83007213
Mol file:100549-95-9.mol

Synonyms:100549-95-9;BRN 5690342;1H-Indol-1-acetic acid, 2,3-dihydro-3,3-diphenyl-2-oxo-5-(((2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)amino)carbonyl)-;2-[5-[(1,5-dimethyl-3-oxo-2-phenylpyrazol-4-yl)carbamoyl]-2-oxo-3,3-diphenylindol-1-yl]acetic acid;5-(4-Antipyrylaminocarbonyl)-2-oxoindoline-1-acetic acid;2-[5-[(1,5-dimethyl-3-oxo-2-phenyl-pyrazol-4-yl)carbamoyl]-2-oxo-3,3-d iphenyl-indol-1-yl]acetic aci;DTXSID70143377;DKVQEGQLWLVCEJ-UHFFFAOYSA-N;LS-82167

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Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1H-Indol-1-acetic acid, 2,3-dihydro-3,3-diphenyl-2-oxo-5-(((2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)amino)carbonyl)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：113.64000
Density:1.44g/cm³
LogP:4.64030
XLogP3:4.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:7
Exact Mass:572.20597001
Heavy Atom Count:43
Complexity:1120

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=O)N(N1C)C2=CC=CC=C2)NC(=O)C3=CC4=C(C=C3)N(C(=O)C4(C5=CC=CC=C5)C6=CC=CC=C6)CC(=O)O

Technology Process of 1H-Indol-1-acetic acid, 2,3-dihydro-3,3-diphenyl-2-oxo-5-(((2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)amino)carbonyl)-

There total 5 articles about 1H-Indol-1-acetic acid, 2,3-dihydro-3,3-diphenyl-2-oxo-5-(((2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)amino)carbonyl)- 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: 95.0%

: 100549-93-7
Ethyl 5-(4-antipyrylaminocarbonyl)-3,3-diphenyl-2-oxoindoline-1-acetate

: 100549-95-9
5-(4-Antipyrylaminocarbonyl)-3,3-diphenyl-2-oxoindoline-1-acetic acid

Guidance literature:: With sodium hydroxide; In ethanol; for 0.5h; Heating;
DOI:10.1007/BF01148381

Reference yield:

: 83-07-8
4-amino-2,3-dimethyl-1-phenylpyrazolin-5-one

: 100549-95-9
5-(4-Antipyrylaminocarbonyl)-3,3-diphenyl-2-oxoindoline-1-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: (C₂H₅)3N / CHCl₃ / 30 min then reflux, 40 min

2: 1.) C₂H₅ONa / 1.) EtOH, toluene, 2.) reflux, 1.5 h

3: 95 percent / NaOH / aq. ethanol / 0.5 h / Heating

With sodium hydroxide; sodium ethanolate; triethylamine; In ethanol; chloroform;
DOI:10.1007/BF01148381

Reference yield:

: 24725-23-3
2-oxo-3,3-diphenyl-2,3-dihydro-indole-5-carboxylic acid

: 100549-95-9
5-(4-Antipyrylaminocarbonyl)-3,3-diphenyl-2-oxoindoline-1-acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: SOCl₂ / 1 h / Heating

2: (C₂H₅)3N / CHCl₃ / 30 min then reflux, 40 min

3: 1.) C₂H₅ONa / 1.) EtOH, toluene, 2.) reflux, 1.5 h

4: 95 percent / NaOH / aq. ethanol / 0.5 h / Heating

With sodium hydroxide; thionyl chloride; sodium ethanolate; triethylamine; In ethanol; chloroform;
DOI:10.1007/BF01148381