90763-40-9

Upstream product

• 90763-34-1 N-(1-Ethyl-pyrrolidin-2-ylmethyl)-2-methoxy-5-(2,2,2-trifluoro-acetylamino)-benzamide 
• 68255-81-2 N-(1-ethyl-2-pyrrolidinylmethyl)-2-methoxy-5-aminobenzamide 
• 23694-03-3 N-(1-ethyl-2-pyrrolidinylmethyl)-2-methoxy-5-nitrobenzamide 
• 90763-46-5 2-methoxy-5-nitrobenzoyl chloride 
• 40751-89-1 2-methoxy-5-nitrobenzoic acid 
• 33581-95-2 tert-butylsulfamyl chloride 
• 90763-37-4 N-(1-Ethyl-pyrrolidin-2-ylmethyl)-2-methoxy-5-methylamino-benzamide 

Downstream Products

• 90763-43-2 C₁₆H₂₆N₄O₄S 

Relevant academic research and scientific papers

Synthesis and Neuroleptic Activity of N--2-methoxy-5-sulfonamidobenzamides

A series of some novel N-benzamides involving replacement of the sulfamoyl group in sulpiride with a sulfonamido group was synthesized and tested for dopamine receptor blockade.In comparison with sulpiride, several compounds were considerably more potent than sulpiride as dopamine receptor blockers.The structure-activity relationships are discussed.