1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide

Base Information

Chemical Name:1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide
CAS No.:169777-65-5
Molecular Formula:C₂₇H₃₅N₅O₄
Molecular Weight:493.606
Hs Code.:

1-<2-<<3-<2-<N-(tert-butoxycarbonyl)amino>ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide

Synonyms:1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide

Suppliers and Price of 1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide

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-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide

There total 5 articles about 1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide 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: 59.0%

: 169777-63-3
1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-nitrophenyl)piperazide

: 169777-65-5
1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 9h; under 760 Torr; Ambient temperature;
DOI:10.1021/jm00018a020

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 169777-65-5
1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / aq. NaOH / 1 h / Ambient temperature

2: 87 percent / K₂CO₃, KI / butan-2-one / 16 h / Heating

3: 59 percent / H₂ / 10percent Pd/C / methanol / 9 h / 760 Torr / Ambient temperature

With sodium hydroxide; hydrogen; potassium carbonate; potassium iodide; palladium on activated charcoal; In methanol; butanone;
DOI:10.1021/jm00018a020

Reference yield:

: 6269-89-2
1-(4-Nitrophenyl)piperazine

: 169777-65-5
1-<2-<<3-<2-ethyl>-1H-indol-5-yl>oxy>acetyl>-4-(4-aminophenyl)piperazide

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / CaCO₃ / butan-2-one / Ambient temperature

2: 87 percent / K₂CO₃, KI / butan-2-one / 16 h / Heating

3: 59 percent / H₂ / 10percent Pd/C / methanol / 9 h / 760 Torr / Ambient temperature

With hydrogen; potassium carbonate; calcium carbonate; potassium iodide; palladium on activated charcoal; In methanol; butanone;
DOI:10.1021/jm00018a020