N-benzyl-N-(2-benzyloxy-5-(2-bromoacetyl)phenyl)methanesulfonamide

Base Information

• Chemical Name: N-benzyl-N-(2-benzyloxy-5-(2-bromoacetyl)phenyl)methanesulfonamide
• CAS No.: 960398-25-8
• Molecular Formula: C₁₆H₁₆BrNO₄S
• Molecular Weight: 398.277
• Mol file: 960398-25-8.mol

Synonyms:N-benzyl-N-(2-benzyloxy-5-(2-bromoacetyl)phenyl)methanesulfonamide

Chemical Property of N-benzyl-N-(2-benzyloxy-5-(2-bromoacetyl)phenyl)methanesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-benzyl-N-(2-benzyloxy-5-(2-bromoacetyl)phenyl)methanesulfonamide

There total 3 articles about N-benzyl-N-(2-benzyloxy-5-(2-bromoacetyl)phenyl)methanesulfonamide 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: 71.0%

N-(5-acetyl-2-benzyloxyphenyl)-N-benzylmethanesulfonamide (960398-24-7) → N-benzyl-N-(2-benzyloxy-5-(2-bromoacetyl)phenyl)methanesulfonamide (960398-25-8)

Guidance literature:

N-(5-acetyl-2-benzyloxyphenyl)-N-benzylmethanesulfonamide; With phenyltrimethylammonium tribromide; In tetrahydrofuran; at 20 ℃; for 14 - 16h;

With sodium hydrogencarbonate; In tetrahydrofuran; water;

Reference yield:

benzyl bromide (100-39-0) → N-benzyl-N-(2-benzyloxy-5-(2-bromoacetyl)phenyl)methanesulfonamide (960398-25-8)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate; sodium iodide / acetone / 15 - 66 h / Heating / reflux

2: phenyltrimethylammonium tribromide / tetrahydrofuran / 14 - 16 h / 20 °C

With phenyltrimethylammonium tribromide; potassium carbonate; sodium iodide; In tetrahydrofuran; acetone;

Reference yield:

1-[4-hydroxy-3-[(methylsulfonyl)amino]phenyl]ethanone (14347-18-3) → N-benzyl-N-(2-benzyloxy-5-(2-bromoacetyl)phenyl)methanesulfonamide (960398-25-8)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate; sodium iodide / acetone / 15 - 66 h / Heating / reflux

2: phenyltrimethylammonium tribromide / tetrahydrofuran / 14 - 16 h / 20 °C

With phenyltrimethylammonium tribromide; potassium carbonate; sodium iodide; In tetrahydrofuran; acetone;

upstream raw materials:

N-(5-acetyl-2-benzyloxyphenyl)-N-benzylmethanesulfonamide

1-[4-hydroxy-3-[(methylsulfonyl)amino]phenyl]ethanone

benzyl bromide

Downstream raw materials:

N-benzyl-N-(2-benzyloxy-5-(2-bromo-1(R)-hydroxyethyl)phenyl)methanesulfonamide

N-benzyl-N-(2-benzyloxy-5-(R)-oxiranylphenyl)methanesulfonamide

C₄₅H₅₃N₃O₆S

(4-(4-(4-(2-(3-(benzylmethanesulfonylamino)-4-benzyloxyphenyl)-2(R)-hydroxyethylamino)butyl)phenyl)butyl)carbamic acid benzyl ester