4(1H)-Pyridinone, 2,3-dihydro-2-phenyl-1-(phenylmethyl)-

Base Information

• Chemical Name: 4(1H)-Pyridinone, 2,3-dihydro-2-phenyl-1-(phenylmethyl)-
• CAS No.: 152873-62-6
• Molecular Formula: C18H17NO
• Molecular Weight: 263.339
• ChEMBL ID: CHEMBL2138771
• DSSTox Substance ID: DTXSID20466245
• Nikkaji Number: J1.927.967G
• Mol file: 152873-62-6.mol

Synonyms:4(1H)-Pyridinone, 2,3-dihydro-2-phenyl-1-(phenylmethyl)-;152873-62-6;MLS002473357;CHEMBL2138771;DTXSID20466245;HMS2217K07;HMS3341B21;SMR001397449;1-benzyl-2-phenyl-2,3-dihydro-1H-pyridin-4-one;1-benzyl-2-phenyl-2,3-dihydro-4(1H)-pyridinone

Chemical Property of 4(1H)-Pyridinone, 2,3-dihydro-2-phenyl-1-(phenylmethyl)-

Chemical Property:

• XLogP3: 3.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 263.131014166
• Heavy Atom Count: 20
• Complexity: 350

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(N(C=CC1=O)CC2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 4(1H)-Pyridinone, 2,3-dihydro-2-phenyl-1-(phenylmethyl)-

There total 8 articles about 4(1H)-Pyridinone, 2,3-dihydro-2-phenyl-1-(phenylmethyl)- 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: 96.0%

danishefsky's diene (54125-02-9) + benzaldehyde (100-52-7) + benzylamine (100-46-9) → N-benzyl-2,3-dihydro-2-phenyl-1H-pyridin-4-one (152873-62-6)

Guidance literature:

With zinc(II) chloride; In dichloromethane; at 30 ℃; for 0.0333333h; Microwave irradiation; Sealed vessel;

DOI:10.1021/jo101219w

Reference yield: 90.0%

danishefsky's diene (54125-02-9) + (E)-N-benzylidenebenzylamine (27845-50-7) → N-benzyl-2,3-dihydro-2-phenyl-1H-pyridin-4-one (152873-62-6)

Guidance literature:

With butyl-methyl-imidazolium triflate; at 30 ℃; for 1h;

DOI:10.1055/s-2005-869837

Reference yield: 86.0%

1-(2-Iodo-benzyl)-2-phenyl-2,3-dihydro-1H-pyridin-4-one (174841-04-4) → N-benzyl-2,3-dihydro-2-phenyl-1H-pyridin-4-one (152873-62-6)

Guidance literature:

With [Pd(OAc)2(PPh₃)2]; tetrabutylammomium bromide; sodium acetate; In N,N-dimethyl-formamide; at 70 ℃;

DOI:10.1016/0040-4039(95)02297-X

upstream raw materials:

danishefsky's diene

N-benzylidene benzylamine

1-(2-Iodo-benzyl)-2-phenyl-2,3-dihydro-1H-pyridin-4-one

(E)-N-benzylidenebenzylamine

Downstream raw materials:

N-benzyl-2-phenyl-5-(4'-(trifluoromethyl)phenyl)-2,3-dihydropyridin-4(1H)-one

N-benzyl-5-(4'-bromophenyl)-2-phenyl-2,3-dihydropyridin-4(1H)-one

N-benzyl-5-(4'-methoxyphenyl)-2-phenyl-2,3-dihydropyridin-4(1H)-one

N-benzyl-5-(4'-chlorophenyl)-2-phenyl-2,3-dihydropyridin-4(1H)-one