4,5-Diphenyl-1,2-dihydropyridin-2-one

Base Information

Chemical Name:4,5-Diphenyl-1,2-dihydropyridin-2-one
CAS No.:110567-94-7
Molecular Formula:C₁₇H₁₃NO
Molecular Weight:247.296
Hs Code.:
European Community (EC) Number:862-897-2

Synonyms:4,5-diphenyl-1,2-dihydropyridin-2-one;110567-94-7;SCHEMBL4717869;4,5-diphenyl-1H-pyridin-2-one;AKOS033867960;EN300-257305;Z2345627922

Suppliers and Price of 4,5-Diphenyl-1,2-dihydropyridin-2-one

Supply Marketing:

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

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of 4,5-Diphenyl-1,2-dihydropyridin-2-one

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:247.099714038
Heavy Atom Count:19
Complexity:396

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC(=O)NC=C2C3=CC=CC=C3

Technology Process of 4,5-Diphenyl-1,2-dihydropyridin-2-one

There total 4 articles about 4,5-Diphenyl-1,2-dihydropyridin-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: 76.8%

: 110567-93-6
2-acetoxy-4,5-diphenylpiridine

: 110567-94-7
4,5-diphenyl-2-pyridone

Guidance literature:: With potassium hydroxide; In methanol; water; for 3h; Ambient temperature;
DOI:10.1021/jo00232a033

Reference yield:

: 110567-82-3,110567-83-4
2,6-diphenyl-2,3-dihydro-4H-thiopyran-4-one oxime

: 110567-94-7
4,5-diphenyl-2-pyridone

Guidance literature:: Multi-step reaction with 5 steps

1: 11.0 g / pyridine; CH₂Cl₂ / Ambient temperature

2: 37 percent / triethylamine / dioxane; H₂O / 6 h / 80 °C

3: MCPBA / CH₂Cl₂ / 1 h / 0 °C

4: 68 percent / acetic anhydride / 1 h / Heating

5: 76.8 percent / potassium hydroxide / methanol; H₂O / 3 h / Ambient temperature

With potassium hydroxide; acetic anhydride; triethylamine; 3-chloro-benzenecarboperoxoic acid; In 1,4-dioxane; pyridine; methanol; dichloromethane; water;
DOI:10.1021/jo00232a033

Reference yield:

: 110567-92-5
2,7-diphenyl-5-oxo-2,3,4,5-tetrahydro-1,4-thiazepine 1-oxide

: 110567-94-7
4,5-diphenyl-2-pyridone

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / acetic anhydride / 1 h / Heating

2: 76.8 percent / potassium hydroxide / methanol; H₂O / 3 h / Ambient temperature

With potassium hydroxide; acetic anhydride; In methanol; water;
DOI:10.1021/jo00232a033