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

Base Information

Chemical Name:3-(1-(3-(3-aminopropoxy)-4-(4-methoxy thiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid
CAS No.:1421328-77-9
Molecular Formula:C₁₉H₂₂N₄O₄S
Molecular Weight:402.474
Hs Code.:

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

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

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

There total 7 articles about 3-(1-(3-(3-aminopropoxy)-4-(4-methoxy thiazol-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: 99.0%

: 1421328-63-3
methyl 3-(1-(3-(3-aminopropoxy)-4-(4-methoxythiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoate

: 1421328-77-9
3-(1-(3-(3-aminopropoxy)-4-(4-methoxy thiazol-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

: 1421328-77-9
3-(1-(3-(3-aminopropoxy)-4-(4-methoxy thiazol-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:

: 105942-08-3
4-bromo-6-fluorobenzonitrile

: 1421328-77-9
3-(1-(3-(3-aminopropoxy)-4-(4-methoxy thiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: potassium hexamethylsilazane / tetrahydrofuran / 6 h / 20 °C / Inert atmosphere

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

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

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

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

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