[((2S,3R)-3-Amino-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid

Base Information

• Chemical Name: [((2S,3R)-3-Amino-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid
• CAS No.: 170936-38-6
• Molecular Formula: C₁₄H₂₂N₂O₄
• Molecular Weight: 282.34
• Mol file: 170936-38-6.mol

Synonyms:[((2S,3R)-3-Amino-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid

Chemical Property of [((2S,3R)-3-Amino-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [((2S,3R)-3-Amino-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid

There total 7 articles about [((2S,3R)-3-Amino-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic 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: 72.0%

[((2S,3R)-3-Azido-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid (170936-48-8) → [((2S,3R)-3-Amino-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid (170936-38-6)

Guidance literature:

With hydrogen; palladium on activated charcoal; In methanol; for 4h; under 775.7 Torr;

Reference yield:

(2R,3R)-2-azido-1-(benzyloxy)-3,4-epoxybutane (115890-32-9) → [((2S,3R)-3-Amino-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid (170936-38-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 83 percent / Et₃N / methanol / 10 h / Heating

2: 72 percent / H₂ / Pd-C / methanol / 4 h / 775.7 Torr

With hydrogen; triethylamine; palladium on activated charcoal; In methanol;

Reference yield:

(2R,3R)-3-azido-4-(benzyloxy)butane-1,2-diol (99884-12-5) → [((2S,3R)-3-Amino-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid (170936-38-6)

Guidance literature:

Multi-step reaction with 4 steps

1: 75 percent / pyridine / 15 h / 0 °C

2: 85 percent / K₂CO₃ / methanol / Ambient temperature

3: 83 percent / Et₃N / methanol / 10 h / Heating

4: 72 percent / H₂ / Pd-C / methanol / 4 h / 775.7 Torr

With hydrogen; potassium carbonate; triethylamine; palladium on activated charcoal; In pyridine; methanol;

upstream raw materials:

[((2S,3R)-3-Azido-4-benzyloxy-2-hydroxy-butyl)-methyl-amino]-acetic acid

(2R,3R)-2-azido-1-(benzyloxy)-3,4-epoxybutane

(2R,3R)-3-azido-4-(benzyloxy)butane-1,2-diol

(1S)-2-(benzyloxy)-1-[(4S)-2,2-dimethyl-1,3-dioxolane-4-yl]-ethan-1-ol

Downstream raw materials:

(6S,7R)-7-Benzyloxymethyl-6-(tert-butyl-diphenyl-silanyloxy)-1,4-dimethyl-[1,4]diazepan-2-one

(6S,7R)-7-Benzyloxymethyl-6-(tert-butyl-diphenyl-silanyloxy)-4-methyl-[1,4]diazepan-2-one

(6S,7R)-7-Benzyloxymethyl-6-hydroxy-4-methyl-[1,4]diazepan-2-one