ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate

Base Information

Chemical Name:ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate
CAS No.:1208318-48-2
Molecular Formula:C₂₆H₂₈N₄O₂
Molecular Weight:428.534
Hs Code.:

Synonyms:ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate

Suppliers and Price of ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate

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 1 raw suppliers

Chemical Property of ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate

There total 8 articles about ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate 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:

: ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-cyano-2-methylphenyl)-1H-pyrrol-2-yl)propanoate

: 1208318-48-2
ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate

Guidance literature:: With sodium tetrahydroborate; cobalt(II) chloride monohydrate; In methanol; at 20 ℃; for 2.5h;

Reference yield:

: 132434-53-8,36715-58-9
1-(4-bromophenyl)-3-(furan-2-yl)-2-propen-1-one

: 1208318-48-2
ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen bromide / 8 h / Reflux

2: toluene-4-sulfonic acid / ethanol / Reflux

3: copper(l) iodide; potassium carbonate; L-proline / dimethyl sulfoxide

With copper(l) iodide; hydrogen bromide; potassium carbonate; toluene-4-sulfonic acid; L-proline; In ethanol; dimethyl sulfoxide;
DOI:10.1016/j.bmcl.2012.01.047

Reference yield:

: 98-01-1
furfural

: 1208318-48-2
ethyl 3-(5-(4-(1H-imidazol-1-yl)phenyl)-1-(4-(aminomethyl)-2-methylphenyl)-1H-pyrrol-2-yl)propanoate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium methylate / methanol / 20 °C

2: hydrogen bromide / 8 h / Reflux

3: toluene-4-sulfonic acid / ethanol / Reflux

4: copper(l) iodide; potassium carbonate; L-proline / dimethyl sulfoxide

With copper(l) iodide; hydrogen bromide; sodium methylate; potassium carbonate; toluene-4-sulfonic acid; L-proline; In methanol; ethanol; dimethyl sulfoxide;
DOI:10.1016/j.bmcl.2012.01.047