1-cyclopropyl-1-(2-(tosylamino)phenyl)(4-bromophenyl)methanol

Base Information

• Chemical Name: 1-cyclopropyl-1-(2-(tosylamino)phenyl)(4-bromophenyl)methanol
• CAS No.: 1334483-25-8
• Molecular Formula: C₂₃H₂₂BrNO₃S
• Molecular Weight: 472.403
• Mol file: 1334483-25-8.mol

Synonyms:1-cyclopropyl-1-(2-(tosylamino)phenyl)(4-bromophenyl)methanol

Chemical Property of 1-cyclopropyl-1-(2-(tosylamino)phenyl)(4-bromophenyl)methanol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-cyclopropyl-1-(2-(tosylamino)phenyl)(4-bromophenyl)methanol

There total 3 articles about 1-cyclopropyl-1-(2-(tosylamino)phenyl)(4-bromophenyl)methanol 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:

cyclopropylmagnesium bromide (23719-80-4) + 2-(4-bromobenzoyl)-1-(4-methylphenylsulfonamido)benzene (370851-82-4) → 1-cyclopropyl-1-(2-(tosylamino)phenyl)(4-bromophenyl)methanol (1334483-25-8)

Guidance literature:

cyclopropylmagnesium bromide; 2-(4-bromobenzoyl)-1-(4-methylphenylsulfonamido)benzene; In tetrahydrofuran; at 20 ℃; Reflux; Inert atmosphere;

With ammonium chloride; In tetrahydrofuran; water; at 20 ℃; for 0.166667h; Inert atmosphere;

DOI:10.1002/chem.201101363

Reference yield:

2-amino-4'-bromobenzophenone (1140-17-6) → 1-cyclopropyl-1-(2-(tosylamino)phenyl)(4-bromophenyl)methanol (1334483-25-8)

Guidance literature:

Multi-step reaction with 2 steps

1.1: pyridine / 20 °C / Inert atmosphere

2.1: tetrahydrofuran / 20 °C / Reflux; Inert atmosphere

2.2: 0.17 h / 20 °C / Inert atmosphere

With pyridine; In tetrahydrofuran;

DOI:10.1002/chem.201101363

Reference yield:

p-toluenesulfonyl chloride (98-59-9) → 1-cyclopropyl-1-(2-(tosylamino)phenyl)(4-bromophenyl)methanol (1334483-25-8)

Guidance literature:

Multi-step reaction with 2 steps

1.1: pyridine / 20 °C / Inert atmosphere

2.1: tetrahydrofuran / 20 °C / Reflux; Inert atmosphere

2.2: 0.17 h / 20 °C / Inert atmosphere

With pyridine; In tetrahydrofuran;

DOI:10.1002/chem.201101363

upstream raw materials:

2-amino-4'-bromobenzophenone

cyclopropylmagnesium bromide

2-(4-bromobenzoyl)-1-(4-methylphenylsulfonamido)benzene

p-toluenesulfonyl chloride

Downstream raw materials:

5-(4-bromophenyl)-1-tosyl-2,3-dihydro-1H-benzo[b]azepine