N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide

Base Information

Chemical Name:N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide
CAS No.:238427-17-3
Molecular Formula:C₂₅H₂₉N₅O₃
Molecular Weight:447.537
Hs Code.:

Synonyms:N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide

Suppliers and Price of N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide

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 N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide

There total 5 articles about N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide 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:

: 42564-36-3
oxo-(2-oxotetrahydrofuran-3-yl)acetic acid ethyl ester

: 238427-17-3
N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: 76 percent / 40 percent HBr / acetic acid / a) reflux, 7 h, b) RT, 48 h

2: oxalyl chloride, DMF / CH₂Cl₂ / 3 h / Ambient temperature

3: pyridine / CH₂Cl₂ / 0 °C

4: 1.5 g / ethanol; H₂O / 2 h / Heating

With pyridine; oxalyl dichloride; hydrogen bromide; N,N-dimethyl-formamide; In ethanol; dichloromethane; water; acetic acid;
DOI:10.1021/jm9706325

Reference yield:

: 57224-27-8
5-bromo-2-oxopentanoic acid

: 238427-17-3
N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl chloride, DMF / CH₂Cl₂ / 3 h / Ambient temperature

2: pyridine / CH₂Cl₂ / 0 °C

3: 1.5 g / ethanol; H₂O / 2 h / Heating

With pyridine; oxalyl dichloride; N,N-dimethyl-formamide; In ethanol; dichloromethane; water;
DOI:10.1021/jm9706325

Reference yield:

: 3-(4-aminophenethyl)-5,5-dimethylimidazolidine-2,4-dione hydrochloride

: 238427-17-3
N-benzyl-3-(2-aminoethyl)-5-<2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) aq. HCl, NaNO₂, 2.) SnCl₂, HCl / 1.) -5-0 deg C, 30 min, 2.) RT, overnight

2: 1.5 g / ethanol; H₂O / 2 h / Heating

With hydrogenchloride; tin(ll) chloride; sodium nitrite; In ethanol; water;
DOI:10.1021/jm9706325