3-chloro-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

Base Information

• Chemical Name: 3-chloro-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one
• CAS No.: 211761-80-7
• Molecular Formula: C₂₁H₂₄ClN₃O₂
• Molecular Weight: 385.893
• Mol file: 211761-80-7.mol

Synonyms:3-chloro-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

Chemical Property of 3-chloro-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-chloro-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

There total 1 articles about 3-chloro-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one 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: 97.0%

3-chloro-2,3,4,5-tetrahydro-1H-<1>benzazepin-2-one (86499-23-2) + 1-(3-aminomethyl-phenyl)-3-isopropyl-urea → 3-chloro-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one (211761-80-7)

Guidance literature:

With potassium hydroxide; tetrabutylammomium bromide; In tetrahydrofuran; for 2h; Ambient temperature;

DOI:10.1021/jm990044m

Reference yield: 59.0%

potassium cyanide (151-50-8) + 3-chloro-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one (211761-80-7) → 3-cyano-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one (239097-58-6)

Guidance literature:

With tetrabutylammomium bromide; In dimethyl sulfoxide; at 115 ℃; for 9h;

DOI:10.1021/jm990044m

Reference yield:

3-chloro-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one (211761-80-7) → 3-(aminomethyl)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one (239097-82-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 59 percent / n-Bu₄NBr / dimethylsulfoxide / 9 h / 115 °C

2: 67 percent / 12N aq. HCl, H₂ / 10 percent Pd/C / ethanol / 2942.03 Torr

With hydrogenchloride; tetrabutylammomium bromide; hydrogen; palladium on activated charcoal; In ethanol; dimethyl sulfoxide;

DOI:10.1021/jm990044m

upstream raw materials:

3-chloro-2,3,4,5-tetrahydro-1H-<1>benzazepin-2-one

Downstream raw materials:

3-cyano-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

3-(hydroxymethyl)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

3-(aminomethyl)-1-N-(3-(N'-(3-isopropylureido))benzyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

1-N-(3-(N'-(3-isopropylureido))benzyl)-3-(methoxycarbonyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one