N-(2-(1-hydroxy-1-phenylhex-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide

Base Information

• Chemical Name: N-(2-(1-hydroxy-1-phenylhex-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide
• CAS No.: 1291079-94-1
• Molecular Formula: C₂₅H₂₅NO₃S
• Molecular Weight: 419.544
• Mol file: 1291079-94-1.mol

Synonyms:N-(2-(1-hydroxy-1-phenylhex-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide

Chemical Property of N-(2-(1-hydroxy-1-phenylhex-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(2-(1-hydroxy-1-phenylhex-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide

There total 2 articles about N-(2-(1-hydroxy-1-phenylhex-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide 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:

1-Pentyne (627-19-0) + 2-(tosylamino)benzophenone (1859-71-8) → N-(2-(1-hydroxy-1-phenylhex-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide (1291079-94-1)

Guidance literature:

1-Pentyne; With ethylmagnesium bromide; In tetrahydrofuran; at 23 - 25 ℃; for 0.25h; Inert atmosphere;

2-(tosylamino)benzophenone; In tetrahydrofuran; for 4h; Inert atmosphere; Reflux;

With water; ammonium chloride; In tetrahydrofuran; Inert atmosphere;

DOI:10.1021/ol2007154

Reference yield:

p-toluenesulfonyl chloride (98-59-9) → N-(2-(1-hydroxy-1-phenylhex-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide (1291079-94-1)

Guidance literature:

Multi-step reaction with 2 steps

1.1: pyridine / 4 h / 23 - 25 °C / Inert atmosphere

2.1: ethylmagnesium bromide / tetrahydrofuran / 0.25 h / 23 - 25 °C / Inert atmosphere

2.2: 4 h / Inert atmosphere; Reflux

2.3: Inert atmosphere

With pyridine; ethylmagnesium bromide; In tetrahydrofuran;

DOI:10.1021/ol2007154

Reference yield: 62.0%

N-(2-(1-hydroxy-1-phenylhex-2-yn-1-yl)phenyl)-4-methylbenzenesulfonamide (1291079-94-1) → 3-iodo-4-phenyl-2-propylquinoline (1291080-08-4)

Guidance literature:

With iodine; In methanol; at 60 ℃; for 12h; regioselective reaction;

DOI:10.1021/ol2007154

upstream raw materials:

1-Pentyne

2-(tosylamino)benzophenone

p-toluenesulfonyl chloride

Downstream raw materials:

3-iodo-4-phenyl-2-propylquinoline