benzyl 3-(3-(benzyloxy)phenyl)-2-(3-(4-(tert-butoxycarbonylamino)benzyl)ureido)propanoate

Base Information

Chemical Name:benzyl 3-(3-(benzyloxy)phenyl)-2-(3-(4-(tert-butoxycarbonylamino)benzyl)ureido)propanoate
CAS No.:1313214-12-8
Molecular Formula:C₃₆H₃₉N₃O₆
Molecular Weight:609.722
Hs Code.:

Synonyms:benzyl 3-(3-(benzyloxy)phenyl)-2-(3-(4-(tert-butoxycarbonylamino)benzyl)ureido)propanoate

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Chemical Property of benzyl 3-(3-(benzyloxy)phenyl)-2-(3-(4-(tert-butoxycarbonylamino)benzyl)ureido)propanoate

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Technology Process of benzyl 3-(3-(benzyloxy)phenyl)-2-(3-(4-(tert-butoxycarbonylamino)benzyl)ureido)propanoate

There total 6 articles about benzyl 3-(3-(benzyloxy)phenyl)-2-(3-(4-(tert-butoxycarbonylamino)benzyl)ureido)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: 68.0%

: 32315-10-9
bis(trichloromethyl) carbonate

: 1313214-11-7
benzyl 2-amino-3-(3-(benzyloxy)phenyl)propanoate

: 220298-96-4
4‐(tert‐butoxycarbonylamino)benzylamine

: 1313214-12-8
benzyl 3-(3-(benzyloxy)phenyl)-2-(3-(4-(tert-butoxycarbonylamino)benzyl)ureido)propanoate

Guidance literature:: bis(trichloromethyl) carbonate; benzyl 2-amino-3-(3-(benzyloxy)phenyl)propanoate; In ethyl acetate; at -10 ℃; Reflux;

4‐(tert‐butoxycarbonylamino)benzylamine; With triethylamine; In ethyl acetate; at 20 ℃;

Reference yield:

: 100-51-6,185532-71-2
benzyl alcohol

: 1313214-12-8
benzyl 3-(3-(benzyloxy)phenyl)-2-(3-(4-(tert-butoxycarbonylamino)benzyl)ureido)propanoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: thionyl chloride / -5 °C

1.2: -5 - 120 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C

3.1: potassium carbonate / acetone / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

5.1: ethyl acetate / -10 °C / Reflux

5.2: 20 °C

With thionyl chloride; potassium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; ethyl acetate; acetone;

Reference yield:

: 775-06-4,29562-33-2
D/L-3-hydroxy-phenylalanine

: 1313214-12-8
benzyl 3-(3-(benzyloxy)phenyl)-2-(3-(4-(tert-butoxycarbonylamino)benzyl)ureido)propanoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: thionyl chloride / -5 °C

1.2: -5 - 120 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C

3.1: potassium carbonate / acetone / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

5.1: ethyl acetate / -10 °C / Reflux

5.2: 20 °C

With thionyl chloride; potassium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; ethyl acetate; acetone;