2,2-Diphenyl-N-(2-piperidin-1-yl-ethyl)-acetamide

Base Information

• Chemical Name: 2,2-Diphenyl-N-(2-piperidin-1-yl-ethyl)-acetamide
• CAS No.: 10120-30-6
• Molecular Formula: C₂₁H₂₆N₂O
• Molecular Weight: 322.45
• DSSTox Substance ID: DTXSID401223815
• Nikkaji Number: J736.112B
• ChEMBL ID: CHEMBL40061
• Mol file: 10120-30-6.mol

Synonyms:CHEMBL40061;DTXSID401223815;BDBM50051977;STK493489;AKOS003404559;PD189131;alpha-Phenyl-N-(2-piperidinoethyl)benzeneacetamide;2,2-Diphenyl-N-(2-piperidin-1-yl-ethyl)-acetamide;2,2-diphenyl-N-[2-(piperidin-1-yl)ethyl]acetamide;alpha-Phenyl-N-[2-(1-piperidinyl)ethyl]benzeneacetamide;2,2-DIPHENYL-N-[2-(1-PIPERIDINYL)ETHYL]ACETAMIDE;10120-30-6

Chemical Property of 2,2-Diphenyl-N-(2-piperidin-1-yl-ethyl)-acetamide

Chemical Property:

• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 322.204513457
• Heavy Atom Count: 24
• Complexity: 348

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1CCN(CC1)CCNC(=O)C(C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 2,2-Diphenyl-N-(2-piperidin-1-yl-ethyl)-acetamide

There total 3 articles about 2,2-Diphenyl-N-(2-piperidin-1-yl-ethyl)-acetamide 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:

2,2-diphenylacetic acid (117-34-0) → diphenyl-acetic acid-(2-piperidino-ethylamide) (10120-30-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 125.8 g / DCC / tetrahydrofuran; dioxane / 16 h / Ambient temperature

2: CH₂Cl₂ / 18 h / 23 °C

With dicyclohexyl-carbodiimide; In tetrahydrofuran; 1,4-dioxane; dichloromethane;

DOI:10.1021/jm950467y

Reference yield:

1-(2-aminoethyl)piperidine (27578-60-5) + 1,7-dimethyl-3,5-dioxo-4-azatricyclo<5.2.1.02,6>dec-8-en-4-yldiphenylacetic acid ester → diphenyl-acetic acid-(2-piperidino-ethylamide) (10120-30-6)

Guidance literature:

In dichloromethane; at 23 ℃; for 18h;

DOI:10.1021/jm950467y

Reference yield:

1-(2-aminoethyl)piperidine (27578-60-5) + diphenylacetic acid chloride (1871-76-7) → diphenyl-acetic acid-(2-piperidino-ethylamide) (10120-30-6)

Guidance literature:

upstream raw materials:

1-(2-aminoethyl)piperidine

diphenylacetic acid chloride

2,2-diphenylacetic acid