[(S)-1-(4-Benzyloxy-benzyl)-3-chloro-2-oxo-propyl]-carbamic acid benzyl ester

Base Information

• Chemical Name: [(S)-1-(4-Benzyloxy-benzyl)-3-chloro-2-oxo-propyl]-carbamic acid benzyl ester
• CAS No.: 56979-29-4
• Molecular Formula: C₂₅H₂₄ClNO₄
• Molecular Weight: 437.923

Synonyms:[(S)-1-(4-Benzyloxy-benzyl)-3-chloro-2-oxo-propyl]-carbamic acid benzyl ester

Chemical Property of [(S)-1-(4-Benzyloxy-benzyl)-3-chloro-2-oxo-propyl]-carbamic acid benzyl ester

Chemical Property:

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Technology Process of [(S)-1-(4-Benzyloxy-benzyl)-3-chloro-2-oxo-propyl]-carbamic acid benzyl ester

There total 4 articles about [(S)-1-(4-Benzyloxy-benzyl)-3-chloro-2-oxo-propyl]-carbamic acid benzyl ester 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:

N-benzyloxycarbonyl-O-benzyl-L-tyrosine (86827-18-1,92455-53-3,16677-29-5) → [(S)-1-(4-Benzyloxy-benzyl)-3-chloro-2-oxo-propyl]-carbamic acid benzyl ester (56979-29-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 4-methylmorpholine / tetrahydrofuran

2: tetrahydrofuran; diethyl ether / 0 °C

3: HCl / dioxane / 0 °C

With 4-methyl-morpholine; hydrogenchloride; In tetrahydrofuran; 1,4-dioxane; diethyl ether;

DOI:10.1021/jm950717a

Reference yield:

benzyl (S)-(1-(4-(benzyloxy)phenyl)-4-diazo-3-oxobutan-2-yl)carbamate → [(S)-1-(4-Benzyloxy-benzyl)-3-chloro-2-oxo-propyl]-carbamic acid benzyl ester (56979-29-4)

Guidance literature:

With hydrogenchloride; In 1,4-dioxane; at 0 ℃; for 1h;

DOI:10.1021/jm00038a005

Reference yield:

C29H31NO7 (1026430-54-5) → [(S)-1-(4-Benzyloxy-benzyl)-3-chloro-2-oxo-propyl]-carbamic acid benzyl ester (56979-29-4)

Guidance literature:

Multi-step reaction with 2 steps

1: tetrahydrofuran; diethyl ether / 0 °C

2: HCl / dioxane / 0 °C

With hydrogenchloride; In tetrahydrofuran; 1,4-dioxane; diethyl ether;

DOI:10.1021/jm950717a

upstream raw materials:

N-benzyloxycarbonyl-O-benzyl-L-tyrosine

C₂₉H₃₁NO₇

Downstream raw materials:

[(S)-2-(4-Benzyloxy-phenyl)-1-(S)-oxiranyl-ethyl]-carbamic acid benzyl ester

{(1S,2R)-1-(4-Benzyloxy-benzyl)-3-[((2R,3S)-3-tert-butoxycarbonylamino-2-hydroxy-4-phenyl-butyl)-(2-trimethylsilanyl-ethoxycarbonyl)-amino]-2-hydroxy-propyl}-carbamic acid benzyl ester

[(2R,3S)-3-tert-Butoxycarbonylamino-2-hydroxy-4-(4-hydroxy-phenyl)-butyl]-((2R,3S)-3-tert-butoxycarbonylamino-2-hydroxy-4-phenyl-butyl)-carbamic acid 2-trimethylsilanyl-ethyl ester

{(1S,2R)-1-Benzyl-3-[(2R,3S)-3-benzyloxycarbonylamino-4-(4-benzyloxy-phenyl)-2-hydroxy-butylamino]-2-hydroxy-propyl}-carbamic acid tert-butyl ester

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