N-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide

Base Information

• Chemical Name: N-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide
• CAS No.: 1338481-63-2
• Molecular Formula: C₁₈H₁₈FN₃O₃S
• Molecular Weight: 375.424
• Mol file: 1338481-63-2.mol

Synonyms:N-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide

Chemical Property of N-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide

There total 5 articles about N-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide 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: 83.0%

(S)-tert-butyl 1-(4-fluoro-2-(3-(methylsulfonyl)phenylamino)phenylamino)-1-oxopropan-2-ylcarbamate (1338481-62-1) + acetic acid (64-19-7,77671-22-8) → N-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide (1338481-63-2)

Guidance literature:

at 100 ℃; for 24h;

DOI:10.1021/acs.jmedchem.5b01651

Reference yield:

3-(methylsulfonyl)aniline (35216-39-8) → N-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide (1338481-63-2)

Guidance literature:

Multi-step reaction with 4 steps

1.1: 92 h / 130 °C

2.1: tin(II) chloride dihdyrate / ethyl acetate / 5 h / Reflux

2.2: 20 °C

3.1: 4-methyl-morpholine; isobutyl chloroformate / dichloromethane / 1 h / -10 °C

3.2: -10 - 20 °C

4.1: 92 h / 100 °C

With 4-methyl-morpholine; tin(II) chloride dihdyrate; isobutyl chloroformate; In dichloromethane; ethyl acetate;

Reference yield:

2,4-Difluoronitrobenzene (446-35-5) → N-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)acetamide (1338481-63-2)

Guidance literature:

Multi-step reaction with 4 steps

1.1: 92 h / 130 °C

2.1: tin(II) chloride dihdyrate / ethyl acetate / 5 h / Reflux

2.2: 20 °C

3.1: 4-methyl-morpholine; isobutyl chloroformate / dichloromethane / 1 h / -10 °C

3.2: -10 - 20 °C

4.1: 92 h / 100 °C

With 4-methyl-morpholine; tin(II) chloride dihdyrate; isobutyl chloroformate; In dichloromethane; ethyl acetate;

upstream raw materials:

3-(methylsulfonyl)aniline

(S)-tert-butyl 1-(4-fluoro-2-(3-(methylsulfonyl)phenylamino)phenylamino)-1-oxopropan-2-ylcarbamate

acetic acid

2,4-Difluoronitrobenzene

Downstream raw materials:

(S)-4-amino-6-((1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethyl)amino)pyrimidine-5-carbonitrile

(R)-4-amino-6-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethylamino)pyrimidine-5-carbonitrile

1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethanamine

4-amino-6-(1-(6-fluoro-1-(3-(methylsulfonyl)phenyl)-1H-benzo[d]imidazol-2-yl)ethylamino)pyrimidine-5-carbonitrile