3-(1-(3-(3-aminopropoxy)-4-(4-phenylthiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid

Base Information

Chemical Name:3-(1-(3-(3-aminopropoxy)-4-(4-phenylthiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid
CAS No.:1421328-80-4
Molecular Formula:C₂₄H₂₄N₄O₃S
Molecular Weight:448.546
Hs Code.:

Synonyms:3-(1-(3-(3-aminopropoxy)-4-(4-phenylthiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid

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Chemical Property of 3-(1-(3-(3-aminopropoxy)-4-(4-phenylthiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid

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Technology Process of 3-(1-(3-(3-aminopropoxy)-4-(4-phenylthiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid

There total 7 articles about 3-(1-(3-(3-aminopropoxy)-4-(4-phenylthiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid 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: 100.0%

: 1421328-65-5
methyl 3-(1-(3-(3-aminopropoxy)-4-(4-isopropoxythiazol-2-yl)phenyl)-1H-imidazol-2-yl)propanoate

: 1421328-80-4
3-(1-(3-(3-aminopropoxy)-4-(4-phenylthiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; methanol; water; at 20 ℃; for 20h; Inert atmosphere;
DOI:10.1016/j.tet.2012.11.070

Reference yield:

: 1093098-93-1
tert-butyl 3-(5-bromo-2-cyanophenoxy)propylcarbamate

: 1421328-80-4
3-(1-(3-(3-aminopropoxy)-4-(4-phenylthiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: L-proline; potassium carbonate; copper(l) iodide / dimethyl sulfoxide / 48 h / 130 °C / Inert atmosphere

2: ammonium sulfide / ethanol / 2 h / 90 °C / Inert atmosphere

3: methanol / 14 h / 90 °C / Inert atmosphere

4: lithium hydroxide / methanol; tetrahydrofuran; water / 20 h / 20 °C / Inert atmosphere

With copper(l) iodide; ammonium sulfide; potassium carbonate; L-proline; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; water; dimethyl sulfoxide;
DOI:10.1016/j.tet.2012.11.070

Reference yield:

: methyl 3-(1H-imidazol-2-yl)propanoate hydrochloride

: 1421328-80-4
3-(1-(3-(3-aminopropoxy)-4-(4-phenylthiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: L-proline; potassium carbonate; copper(l) iodide / dimethyl sulfoxide / 48 h / 130 °C / Inert atmosphere

2: ammonium sulfide / ethanol / 2 h / 90 °C / Inert atmosphere

3: methanol / 14 h / 90 °C / Inert atmosphere

4: lithium hydroxide / methanol; tetrahydrofuran; water / 20 h / 20 °C / Inert atmosphere

With copper(l) iodide; ammonium sulfide; potassium carbonate; L-proline; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; water; dimethyl sulfoxide;
DOI:10.1016/j.tet.2012.11.070