2-{[2-(3-amino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic acid

Base Information

Chemical Name:2-{[2-(3-amino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic acid
CAS No.:623174-42-5
Molecular Formula:C₂₈H₃₈N₂O₇
Molecular Weight:514.619
Hs Code.:

2-{[2-(3-amino-propionyloxy)-3-<i>tert</i>-butoxy-benzyl]-<i>tert</i>-butoxycarbonyl-amino}-3-phenyl-propionic acid

Synonyms:2-{[2-(3-amino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic acid

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Chemical Property of 2-{[2-(3-amino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic acid

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Technology Process of 2-{[2-(3-amino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic acid

There total 7 articles about 2-{[2-(3-amino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic 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: 80.0%

: 623174-51-6
2-{[2-(3-benzyloxycarbonylamino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic acid benzyl ester

: 623174-42-5
2-{[2-(3-amino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; isopropyl alcohol;
DOI:10.1039/b303836j

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 623174-42-5
2-{[2-(3-amino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / CH₂Cl₂ / 16 h

2: 71 percent / DCC; DMAP / CH₂Cl₂

3: 80 percent / H₂ / Pd/C / ethyl acetate; propan-2-ol

With dmap; hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal; In dichloromethane; ethyl acetate; isopropyl alcohol;
DOI:10.1039/b303836j

Reference yield:

: 24677-78-9
2,3-dihydroxybenzaldehyde

: 623174-42-5
2-{[2-(3-amino-propionyloxy)-3-tert-butoxy-benzyl]-tert-butoxycarbonyl-amino}-3-phenyl-propionic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 35 percent / trifluoromethanesulfonic acid / benzene; CH₂Cl₂ / 7 h / -60 °C

2: 80 percent / Na(OAc)3BH / tetrahydrofuran / 16 h

3: 80 percent / CH₂Cl₂ / 16 h

4: 71 percent / DCC; DMAP / CH₂Cl₂

5: 80 percent / H₂ / Pd/C / ethyl acetate; propan-2-ol

With dmap; trifluorormethanesulfonic acid; hydrogen; sodium tris(acetoxy)borohydride; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; ethyl acetate; isopropyl alcohol; benzene;
DOI:10.1039/b303836j