31376-45-1

Upstream product

• 40447-04-9 N-(3-chloro-2-methylphenyl)benzamide 

Downstream Products

• 1609460-40-3 N-benzyl-N'-(3-chloro-2-methylphenyl)benzimidamide 
• 42311-78-4 N-[3-Chloro-2-({[(cyclohexyl-methyl-carbamoyl)-methyl]-methyl-amino}-methyl)-phenyl]-benzamide 
• 42311-73-9 N-[3-Chloro-2-({[(3-dimethylamino-propylcarbamoyl)-methyl]-methyl-amino}-methyl)-phenyl]-benzamide 
• 40718-92-1 N-(2-{[(Benzylcarbamoyl-methyl)-methyl-amino]-methyl}-3-chloro-phenyl)-benzamide 
• 41458-70-2 6-Chlor-2-dibenzoylaminobenzylbromid 
• 18053-30-0 [(2-Benzoylamino-6-chloro-benzyl)-methyl-amino]-acetic acid 
• 18053-42-4 N-{3-Chloro-2-[(methyl-phenylcarbamoylmethyl-amino)-methyl]-phenyl}-benzamide 
• 18285-81-9 N-(3-Chloro-2-{[(isopropylcarbamoyl-methyl)-methyl-amino]-methyl}-phenyl)-benzamide 
• 18053-43-5 N-{3-Chloro-2-[(diethylcarbamoylmethyl-methyl-amino)-methyl]-phenyl}-benzamide 

Relevant academic research and scientific papers

Solvent/oxidant-switchable synthesis of multisubstituted quinazolines and benzimidazoles via metal-free selective oxidative annulation of arylamidines

A fast and simple divergent synthesis of multisubstituted quinazolines and benzimidazoles was developed from readily available amidines, via iodine(III)-promoted oxidative C(sp3)-C(sp2) and C(sp 2)-N bond formation in nonpolar and polar solvents, respectively. Further selective synthesis of quinazolines in polar solvent was realized by TEMPO-catalyzed sp3C-H/sp2C-H direct coupling of the amidine with K2S2O8 as the oxidant. No metal, base, or other additives were needed.