4-cyclopentyl-N-ethyl-N-(2-piperidin-1-ylethyl)aniline

Base Information

• Chemical Name: 4-cyclopentyl-N-ethyl-N-(2-piperidin-1-ylethyl)aniline
• CAS No.: 94358-16-4
• Molecular Formula: C20H32N2
• Molecular Weight: 300.48100
• DSSTox Substance ID: DTXSID90361197
• Wikidata: Q82143403
• Mol file: 94358-16-4.mol

Synonyms:94358-16-4;4-cyclopentyl-N-ethyl-N-(2-piperidin-1-ylethyl)aniline;AE-641/30116041;Oprea1_729554;DTXSID90361197;AKOS005066155;4-cyclopentyl-N-ethyl-N-[2-(1-piperidinyl)ethyl]aniline

Chemical Property of 4-cyclopentyl-N-ethyl-N-(2-piperidin-1-ylethyl)aniline

Chemical Property:

• PSA: 6.48000
• LogP: 4.59430
• XLogP3: 5.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 300.256549029
• Heavy Atom Count: 22
• Complexity: 297

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN(CCN1CCCCC1)C2=CC=C(C=C2)C3CCCC3

Technology Process of 4-cyclopentyl-N-ethyl-N-(2-piperidin-1-ylethyl)aniline

There total 4 articles about 4-cyclopentyl-N-ethyl-N-(2-piperidin-1-ylethyl)aniline 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: 99.0%

N-(4-Cyclopentyl-phenyl)-N-ethyl-2-piperidin-1-yl-acetamide (85603-19-6) → (4-Cyclopentyl-phenyl)-ethyl-(2-piperidin-1-yl-ethyl)-amine (94358-16-4)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; benzene; for 5h; Heating;

DOI:10.1135/cccc19830156

Reference yield:

N-(4-Cyclopentylphenyl)acetamide (85602-98-8) → (4-Cyclopentyl-phenyl)-ethyl-(2-piperidin-1-yl-ethyl)-amine (94358-16-4)

Guidance literature:

Multi-step reaction with 4 steps

1: 97 percent / LiAlH₄ / benzene; diethyl ether / 5 h / Heating

2: 100 percent / K₂CO₃ / CHCl₃ / 1.5 h / Heating

3: 83 percent / benzene / 6 h / Heating

4: 99 percent / LiAlH₄, / benzene; diethyl ether / 5 h / Heating

With lithium aluminium tetrahydride; potassium carbonate; In diethyl ether; chloroform; benzene;

DOI:10.1135/cccc19830156

Reference yield:

N-Ethyl-4-cyclopentylaniline (85603-06-1) → (4-Cyclopentyl-phenyl)-ethyl-(2-piperidin-1-yl-ethyl)-amine (94358-16-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 100 percent / K₂CO₃ / CHCl₃ / 1.5 h / Heating

2: 83 percent / benzene / 6 h / Heating

3: 99 percent / LiAlH₄, / benzene; diethyl ether / 5 h / Heating

With lithium aluminium tetrahydride; potassium carbonate; In diethyl ether; chloroform; benzene;

DOI:10.1135/cccc19830156

upstream raw materials:

N-(4-Cyclopentyl-phenyl)-N-ethyl-2-piperidin-1-yl-acetamide

N-(4-Cyclopentylphenyl)acetamide

N-Ethyl-4-cyclopentylaniline

N-(4-cyclopentylphenyl)-N-ethylchloroacetamide