[(1S,2R)-1-benzyl-3-benzylamino-2-(tetrahydropyran-2-yloxy)propyl]carbamic acid benzyl ester

Base Information

• Chemical Name: [(1S,2R)-1-benzyl-3-benzylamino-2-(tetrahydropyran-2-yloxy)propyl]carbamic acid benzyl ester
• CAS No.: 1190630-76-2
• Molecular Formula: C₃₀H₃₆N₂O₄
• Molecular Weight: 488.627
• Mol file: 1190630-76-2.mol

Synonyms:[(1S,2R)-1-benzyl-3-benzylamino-2-(tetrahydropyran-2-yloxy)propyl]carbamic acid benzyl ester

Chemical Property of [(1S,2R)-1-benzyl-3-benzylamino-2-(tetrahydropyran-2-yloxy)propyl]carbamic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [(1S,2R)-1-benzyl-3-benzylamino-2-(tetrahydropyran-2-yloxy)propyl]carbamic acid benzyl ester

There total 9 articles about [(1S,2R)-1-benzyl-3-benzylamino-2-(tetrahydropyran-2-yloxy)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: 97.0%

(2R,3S)-3-amino-2-tetrahydropyranyloxy-4-phenyl-1-benzylaminobutane (1190630-75-1) + benzyl chloroformate (501-53-1,94274-21-2) → [(1S,2R)-1-benzyl-3-benzylamino-2-(tetrahydropyran-2-yloxy)propyl]carbamic acid benzyl ester (1190630-76-2)

Guidance literature:

With sodium hydrogencarbonate; In diethyl ether; water; at 0 ℃; for 5h;

DOI:10.1021/ml300197h

Reference yield:

(3S)-3-azido-2-tetrahydropyranyloxy-4-phenylbutan-1-yl p-toluenesulfonate → [(1S,2R)-1-benzyl-3-benzylamino-2-(tetrahydropyran-2-yloxy)propyl]carbamic acid benzyl ester (1190630-76-2)

Guidance literature:

Multi-step reaction with 3 steps

1: tetrahydrofuran / 56 h / 90 °C

2: hydrogen / palladium 10% on activated carbon / methanol / 12 h

3: sodium hydrogencarbonate / diethyl ether / 0 °C

With hydrogen; sodium hydrogencarbonate; palladium 10% on activated carbon; In tetrahydrofuran; methanol; diethyl ether;

Reference yield:

C17H19N3O4S → [(1S,2R)-1-benzyl-3-benzylamino-2-(tetrahydropyran-2-yloxy)propyl]carbamic acid benzyl ester (1190630-76-2)

Guidance literature:

Multi-step reaction with 4 steps

1: pyridinium p-toluenesulfonate / dichloromethane / 24 h

2: tetrahydrofuran / 56 h / 90 °C

3: hydrogen / palladium 10% on activated carbon / methanol / 12 h

4: sodium hydrogencarbonate / diethyl ether / 0 °C

With hydrogen; pyridinium p-toluenesulfonate; sodium hydrogencarbonate; palladium 10% on activated carbon; In tetrahydrofuran; methanol; diethyl ether; dichloromethane;

upstream raw materials:

(2R,3S)-3-amino-2-tetrahydropyranyloxy-4-phenyl-1-benzylaminobutane

benzyl chloroformate

3(S)-azido-4-phenyl-1-(p-toluenesulphonyloxy)-2(S)-butanol

(2S,3S)-2-azido-1-phenyl-butane-3,4-diol

Downstream raw materials:

(2R,3S)-3-Cbz-amino-2-hydroxy-4-phenyl-1-benzylaminobutane

C₃₄H₄₀N₂O₆

(2R,3S)-3-Cbz-amino-2-hydroxy-4-phenyl-1-(N-benzyl-2-diazo-ethanamido)butane

(2R,3S)-3-Cbz-amino-2-hydroxy-4-phenyl-1-(N-benzylacetamido)butane