1-(4,4-Bis(4-fluorophenyl)butyl)-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine

Base Information

• Chemical Name: 1-(4,4-Bis(4-fluorophenyl)butyl)-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine
• CAS No.: 143759-64-2
• Molecular Formula: C₃₀H₃₇F₂N₃O
• Molecular Weight: 493.64
• DSSTox Substance ID: DTXSID60932015
• Nikkaji Number: J1.766.511A
• ChEMBL ID: CHEMBL61492
• Mol file: 143759-64-2.mol

Synonyms:1-(4,4-Bis(4-fluorophenyl)butyl)-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine;1-Piperazineethanol, 4-(4,4-bis(4-fluorophenyl)butyl)-alpha-(((phenylmethyl)amino)methyl)-;4-(4,4-Bis(4-fluorophenyl)butyl)-alpha-(((phenylmethyl)amino)methyl)-1-piperazineethanol;143759-64-2;1-[4,4-Bis(4-fluorophenyl)butyl]-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine;CHEMBL61492;SCHEMBL7751327;C30H37F2N3O;DTXSID60932015;LWPSLBQTDYKNEJ-UHFFFAOYSA-N;LS-112101;1-[4-[4,4-Bis(4-fluorophenyl)butyl]piperazino]-3-(benzylamino)-2-propanol;1-(Benzylamino)-3-{4-[4,4-bis(4-fluorophenyl)butyl]piperazin-1-yl}propan-2-ol

Chemical Property of 1-(4,4-Bis(4-fluorophenyl)butyl)-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine

Chemical Property:

• Vapor Pressure: 3.59E-16mmHg at 25°C
• Boiling Point: 618.8°Cat760mmHg
• Flash Point: 328°C
• Density: 1.147g/cm³
• XLogP3: 4.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 12
• Exact Mass: 493.29046914
• Heavy Atom Count: 36
• Complexity: 559

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CN(CCN1CCCC(C2=CC=C(C=C2)F)C3=CC=C(C=C3)F)CC(CNCC4=CC=CC=C4)O

Technology Process of 1-(4,4-Bis(4-fluorophenyl)butyl)-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine

There total 3 articles about 1-(4,4-Bis(4-fluorophenyl)butyl)-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine 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: 62.0%

N-benzyl-3-amino-1-chloropropan-2-ol (75605-52-6,278788-93-5) + 1-[4,4-bis(4-fluorophenyl)butyl]piperazine (5631-35-6) → 1-[4,4-Bis(4-fluorophenyl)butyl]-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine (143759-64-2)

Guidance literature:

With potassium carbonate; potassium iodide; In ethanol;

DOI:10.1016/S0960-894X(02)00322-0

Reference yield:

benzylamine (100-46-9) + 1-[4,4-bis(4-fluorophenyl)butyl]-4-(2,3-epoxypropyl)piperazine (143759-57-3) → 1-[4,4-Bis(4-fluorophenyl)butyl]-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine (143759-64-2)

Guidance literature:

In N,N-dimethyl-formamide;

Reference yield:

benzylamine (100-46-9) → 1-[4,4-Bis(4-fluorophenyl)butyl]-4-(2-hydroxy-3-phenylmethylaminopropyl)piperazine (143759-64-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 46 percent / ethanol / Heating

2: 62 percent / potassium carbonate; potassium iodide / ethanol / Heating

With potassium carbonate; potassium iodide; In ethanol;

DOI:10.1016/S0968-0896(03)00428-0

upstream raw materials:

N-benzyl-3-amino-1-chloropropan-2-ol

1-[4,4-bis(4-fluorophenyl)butyl]piperazine

benzylamine

1-[4,4-bis(4-fluorophenyl)butyl]-4-(2,3-epoxypropyl)piperazine