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

Base Information

Chemical Name:methyl 3-(1-(3-(3-aminopropoxy)-4-(4-methoxythiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoate
CAS No.:1421328-63-3
Molecular Formula:C₂₀H₂₄N₄O₄S
Molecular Weight:416.501
Hs Code.:

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

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Chemical Property of methyl 3-(1-(3-(3-aminopropoxy)-4-(4-methoxythiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoate

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Technology Process of methyl 3-(1-(3-(3-aminopropoxy)-4-(4-methoxythiazol-2-yl) phenyl)-1H-imidazol-2-yl) propanoate

There total 8 articles about methyl 3-(1-(3-(3-aminopropoxy)-4-(4-methoxythiazol-2-yl) phenyl)-1H-imidazol-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: 99.0%

: 1421328-92-8
C₂₅H₃₂N₄O₆S

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

Guidance literature:: With trifluoroacetic acid; In dichloromethane; Inert atmosphere;
DOI:10.1016/j.tet.2012.11.070

Reference yield: 78.0%

: 1093098-95-3
methyl 3-(1-(3-(3-(tert-butoxycarbonyl amino)propoxy)-4-carbamothioylphenyl)-1H-imidazol-2-yl) propanoate

: 96-34-4
methyl chloroacetate

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

Guidance literature:: In methanol; at 90 ℃; for 14h; Inert atmosphere;
DOI:10.1016/j.tet.2012.11.070

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 3 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

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