21143-53-3

Upstream product

• 67-56-1 methanol 
• 81992-90-7 2-benzyl-4-chloro-benzoic acid 
• 1666-17-7 benzaldehyde p-toluenesulfonylhydrazone 
• 84459-33-6 2-bromo-4-chlorobenzaldehyde 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 1426547-46-7 5-chloro-2-formylphenyl trifluoromethanesulfonate 
• 33184-56-4 2-benzoyl-4-chlorobenzoic acid 
• 21143-54-4 2-Benzyl-4-chlorobenzyl alcohol 
• 81992-91-8 2-benzyl-4-chlorobenzaldehyde 

Downstream Products

• 21143-54-4 2-Benzyl-4-chlorobenzyl alcohol 
• 83562-01-0 3-oxo-3-(4-chloro-2-benzylphenyl)propanenitrile 
• 83562-02-1 3-(2-Benzyl-4-chloro-phenyl)-2-bromo-3-oxo-propionitrile 
• 78368-02-2 8-chloro-6-phenyl-4H-thiazolo<5,4-d><2>benzazepin-2-amine 
• 83562-03-2 2-amino-4-(2-benzyl-4-chlorophenyl)-5-thiazolecarbonitrile 
• 83562-06-5 N-(8-chloro-6-phenyl-4H-thiazolo<5,4-d><2>benzazepin-2-yl)acetamide 
• 83562-04-3 N-<4-(2-benzyl-4-chlorophenyl)-5-cyanothiazol-2-yl>acetamide 
• 83562-05-4 N-<4-(2-benzoyl-4-chlorophenyl)-5-cyanothiazol-2-yl>acetamide 
• 21143-57-7 (2-Benzyl-4-chloro-phenyl)-acetic acid 
• 21143-56-6 (2-Benzyl-4-chloro-phenyl)-acetonitrile 
• 21143-55-5 2-Benzyl-1-bromomethyl-4-chloro-benzene 

Relevant academic research and scientific papers

Palladium-Catalyzed Three-Component Coupling Reaction of o-Bromobenzaldehyde, N-Tosylhydrazone, and Methanol

A ligand-controlled palladium-catalyzed three-component reaction of o-bromobenzaldehyde, N-tosylhydrazone, and methanol is described. This reaction uses readily available compounds as starting materials while displaying a broad substrate scope and good functional group compatibility.

2-Benzazepines. 2. Thiazolobenzazepines

As part of a program in the area of annelated 2-benzazepines, several thiazolobenzazepines were prepared.Treatment of the bromo ketones 7-9 with various thio amides gave the thiazoles 10-15, which when treated with methylamine gave the title com