(2R)-2-{benzyl[(6-{[benzyl-(2R)-(1-hydroxy-3-phenylpropan-2-yl)amino]methyl}pyridin-2-yl)methyl]amino}-3-phenylpropan-1-ol

Base Information

• Chemical Name: (2R)-2-{benzyl[(6-{[benzyl-(2R)-(1-hydroxy-3-phenylpropan-2-yl)amino]methyl}pyridin-2-yl)methyl]amino}-3-phenylpropan-1-ol
• CAS No.: 1329682-32-7
• Molecular Formula: C₃₉H₄₃N₃O₂
• Molecular Weight: 585.789
• Mol file: 1329682-32-7.mol

Synonyms:(2R)-2-{benzyl[(6-{[benzyl-(2R)-(1-hydroxy-3-phenylpropan-2-yl)amino]methyl}pyridin-2-yl)methyl]amino}-3-phenylpropan-1-ol

Chemical Property of (2R)-2-{benzyl[(6-{[benzyl-(2R)-(1-hydroxy-3-phenylpropan-2-yl)amino]methyl}pyridin-2-yl)methyl]amino}-3-phenylpropan-1-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R)-2-{benzyl[(6-{[benzyl-(2R)-(1-hydroxy-3-phenylpropan-2-yl)amino]methyl}pyridin-2-yl)methyl]amino}-3-phenylpropan-1-ol

There total 5 articles about (2R)-2-{benzyl[(6-{[benzyl-(2R)-(1-hydroxy-3-phenylpropan-2-yl)amino]methyl}pyridin-2-yl)methyl]amino}-3-phenylpropan-1-ol 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%

2,6-bis-(bromomethyl)pyridine (7703-74-4) + (2R)-(+)-2-benzylamino-3-phenylpropan-1-ol (60046-47-1) → (2R)-2-{benzyl[(6-{[benzyl-(2R)-(1-hydroxy-3-phenylpropan-2-yl)amino]methyl}pyridin-2-yl)methyl]amino}-3-phenylpropan-1-ol (1329682-32-7)

Guidance literature:

With sodium carbonate; potassium iodide; In ethanol; at 100 ℃; for 12h; Further stages; Inert atmosphere;

DOI:10.1002/aoc.3416

Reference yield:

(R)-2-amino-3-phenylpropanol (5267-64-1) → (2R)-2-{benzyl[(6-{[benzyl-(2R)-(1-hydroxy-3-phenylpropan-2-yl)amino]methyl}pyridin-2-yl)methyl]amino}-3-phenylpropan-1-ol (1329682-32-7)

Guidance literature:

Multi-step reaction with 3 steps

1: methanol / Reflux; Inert atmosphere

2: sodium tetrahydroborate / methanol / Inert atmosphere

3: sodium carbonate; potassium iodide / ethanol / 12 h / 100 °C / Inert atmosphere

With sodium tetrahydroborate; sodium carbonate; potassium iodide; In methanol; ethanol;

DOI:10.1016/j.tet.2011.06.064

Reference yield:

D-(R)-phenylalanine (673-06-3,25191-15-5,658-69-5,67675-33-6) → (2R)-2-{benzyl[(6-{[benzyl-(2R)-(1-hydroxy-3-phenylpropan-2-yl)amino]methyl}pyridin-2-yl)methyl]amino}-3-phenylpropan-1-ol (1329682-32-7)

Guidance literature:

Multi-step reaction with 4 steps

1: sodium tetrahydroborate; iodine / tetrahydrofuran / Inert atmosphere

2: methanol / Reflux; Inert atmosphere

3: sodium tetrahydroborate / methanol / Inert atmosphere

4: sodium carbonate; potassium iodide / ethanol / 12 h / 100 °C / Inert atmosphere

With sodium tetrahydroborate; iodine; sodium carbonate; potassium iodide; In tetrahydrofuran; methanol; ethanol;

DOI:10.1016/j.tet.2011.06.064

upstream raw materials:

2,6-bis-(bromomethyl)pyridine

(2R)-(+)-2-benzylamino-3-phenylpropan-1-ol

(R)-2-amino-3-phenylpropanol

D-(R)-phenylalanine

Downstream raw materials:

(5R,15R)-5,6,14,15-tetrabenzyl-3,17-dioxa-6,14,23,24-tetraazatricyclo[17.3.1.1(8,12)]tetracosa-1⁽²³⁾,8,10,12⁽²⁴⁾,19,21-hexaene