(1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine

Base Information

Chemical Name:(1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine
CAS No.:98245-08-0
Molecular Formula:C₂₅H₃₄N₄
Molecular Weight:390.572
Hs Code.:

Synonyms:(1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine

Suppliers and Price of (1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine

There total 11 articles about (1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine 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:

: 39742-60-4
1-(2-phenylethyl)-4-piperidinone

: 98245-08-0
(1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / H₂ / 10 percent Pd/C / methanol / 760 Torr / Ambient temperature

2: 84 percent / tetrahydrofuran; ethanol / 25 °C

3: 98.4 percent / H₂, ammonia / 5 percent Pd/C / methanol / 760 Torr / Ambient temperature

4: 18 percent / mercury oxide, sulfur / ethanol / 2 h / Heating

5: 1.) sodium hydride / 1.) dimethyl sulfoxide, benzene, 30 min, 2.) dimethyl sulfoxide, benzene, RT, overnight

With ammonia; hydrogen; sodium hydride; sulfur; mercury(II) oxide; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol;
DOI:10.1021/jm00150a029

Reference yield:

: 2719-30-4
o-nitrophenylisothiocyanate

: 98245-08-0
(1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine

Guidance literature:: Multi-step reaction with 6 steps

1: tetrahydrofuran / 25 °C

2: H₂, NH₃ / 10 percent Pd/C / methanol / 760 Torr / Ambient temperature

3: HgO/S

4: 48 percent aq. HBr / 2 h / 120 °C

5: Na₂CO₃ / dimethylformamide / 70 °C

6: 1.) sodium hydride / 1.) dimethyl sulfoxide, benzene, 30 min, 2.) dimethyl sulfoxide, benzene, RT, overnight

With ammonia; hydrogen bromide; hydrogen; sodium hydride; sodium carbonate; sulfur; mercury(II) oxide; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00150a029

Reference yield:

: 73733-91-2
N-(1-methylethyl)-1-(2-phenylethyl)-4-piperidinamine

: 98245-08-0
(1-Ethyl-1H-benzoimidazol-2-yl)-isopropyl-(1-phenethyl-piperidin-4-yl)-amine

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / tetrahydrofuran; ethanol / 25 °C

2: 98.4 percent / H₂, ammonia / 5 percent Pd/C / methanol / 760 Torr / Ambient temperature

3: 18 percent / mercury oxide, sulfur / ethanol / 2 h / Heating

4: 1.) sodium hydride / 1.) dimethyl sulfoxide, benzene, 30 min, 2.) dimethyl sulfoxide, benzene, RT, overnight

With ammonia; hydrogen; sodium hydride; sulfur; mercury(II) oxide; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol;
DOI:10.1021/jm00150a029