N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-2-phenylquinoline-4-carboxamide

Base Information

Chemical Name:N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-2-phenylquinoline-4-carboxamide
CAS No.:1752-99-4
Molecular Formula:C₂₇H₂₂N₄O₂
Molecular Weight:434.497
Hs Code.:
DSSTox Substance ID:DTXSID901120743
ChEMBL ID:CHEMBL1698622

Synonyms:N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-2-phenylquinoline-4-carboxamide;N-(1,5-dimethyl-3-oxo-2-phenylpyrazol-4-yl)-2-phenylquinoline-4-carboxamide;1752-99-4;Oprea1_396550;MLS002253026;CHEMBL1698622;TVYOZMHVVVTKLT-UHFFFAOYSA-N;DTXSID901120743;HMS3082P10;STK956690;AKOS001030193;SMR001315355;AE-848/09805006;SR-01000025520;SR-01000025520-1;Z27661926;N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-2-phenyl-4-quinolinecarboxamide;N-(2,3-Dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)-2-phenyl-4-quinolinecarboxamide

Suppliers and Price of N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-2-phenylquinoline-4-carboxamide

Supply Marketing:

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

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Chemical Property of N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-2-phenylquinoline-4-carboxamide

Chemical Property:

XLogP3:5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:434.17427596
Heavy Atom Count:33
Complexity:768

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C(=O)N(N1C)C2=CC=CC=C2)NC(=O)C3=CC(=NC4=CC=CC=C43)C5=CC=CC=C5

Technology Process of N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-2-phenylquinoline-4-carboxamide

There total 6 articles about N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-2-phenylquinoline-4-carboxamide 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: 70.0%

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

: 132-60-5
cinchophen

: 1752-99-4
2-phenyl-N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-quinoline-4-carboxamide

Guidance literature:: With trichlorophosphate; for 8h; Reflux;
DOI:10.14233/ajchem.2020.22583

Reference yield:

: 91-56-5,1186480-61-4,84788-92-1
indole-2,3-dione

: 1752-99-4
2-phenyl-N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-quinoline-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol / 12 h / Reflux

2: trichlorophosphate / 8 h / Reflux

With sodium hydroxide; trichlorophosphate; In ethanol; 1: |Pfitzinger Quinoline Synthesis;
DOI:10.14233/ajchem.2020.22583

Reference yield:

: 98-86-2
acetophenone

: 1752-99-4
2-phenyl-N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-quinoline-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol / 12 h / Reflux

2: trichlorophosphate / 8 h / Reflux

With sodium hydroxide; trichlorophosphate; In ethanol; 1: |Pfitzinger Quinoline Synthesis;
DOI:10.14233/ajchem.2020.22583