N-(3-bromobenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)acetamide

Base Information

• Chemical Name: N-(3-bromobenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)acetamide
• CAS No.: 1590398-21-2
• Molecular Formula: C₁₈H₂₀BrFN₂O₃S
• Molecular Weight: 443.337
• Mol file: 1590398-21-2.mol

Synonyms:N-(3-bromobenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)acetamide

Chemical Property of N-(3-bromobenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(3-bromobenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)acetamide

There total 3 articles about N-(3-bromobenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)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: 60.0%

[(4-fluorobenzenesulfonyl)(isopropyl)amino]acetic acid (1178934-09-2) + 3-bromobenzylamine (10269-01-9) → N-(3-bromobenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)acetamide (1590398-21-2)

Guidance literature:

With triethylamine; HATU; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

N-(2-propyl)glycine methyl ester → N-(3-bromobenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)acetamide (1590398-21-2)

Guidance literature:

Multi-step reaction with 3 steps

1: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C

2: lithium hydroxide; water / tetrahydrofuran / 1 h / 20 °C

3: triethylamine; HATU / dichloromethane / 2 h / 20 °C

With dmap; water; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; In tetrahydrofuran; dichloromethane;

Reference yield:

methyl 2-(4-fluoro-N-isopropylphenylsulfonamido)acetate (1184709-74-7) → N-(3-bromobenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)acetamide (1590398-21-2)

Guidance literature:

Multi-step reaction with 2 steps

1: lithium hydroxide; water / tetrahydrofuran / 1 h / 20 °C

2: triethylamine; HATU / dichloromethane / 2 h / 20 °C

With water; triethylamine; HATU; lithium hydroxide; In tetrahydrofuran; dichloromethane;

upstream raw materials:

[(4-fluorobenzenesulfonyl)(isopropyl)amino]acetic acid

3-bromobenzylamine

methyl 2-(4-fluoro-N-isopropylphenylsulfonamido)acetate

Downstream raw materials:

N-(3-cyclopropylbenzyl)-2-(4-fluoro-N-isopropylphenylsulfonamido)acetamide

(+/-)-2-(4-fluoro-N-isopropylphenylsulfonamido)-N-(3-(2-(2-methylpyrrolidin-1-yl)pyrimidin-5-yl)benzyl)acetamide

(S)-2-(4-fluoro-N-isopropylphenylsulfonamido)-N-(3-(2-(2-methylpyrrolidin-1-yl)pyrimidin-5-yl)benzyl)acetamide

(R)-2-(4-fluoro-N-isopropylphenylsulfonamido)-N-(3-(2-(2-methylpyrrolidin-1-yl)pyrimidin-5-yl)benzyl)acetamide