90763-35-2

Upstream product

• 68255-94-7 N-(1-ethyl-2-pyrrolidinylmethyl)-2-methoxy-4-methyl-5-aminobenzamide 
• 407-25-0 trifluoroacetic anhydride 
• 26116-12-1 1-ethyl-2-pyrrolidinemethanamine 
• 90763-12-5 2-methoxy-4-methyl-5-nitrobenzoic acid 
• 90763-30-7 N-(1-Ethyl-pyrrolidin-2-ylmethyl)-2-methoxy-4-methyl-5-nitro-benzamide 
• 68256-33-7 2-methoxy-4-methyl-5-nitrobenzoyl chloride 

Downstream Products

• 90763-41-0 N-<(1-ethyl-2-pyrrolidinyl)methyl>-2-methoxy-4-methyl-5-<(tert-butylsulfamoyl)methylamino>benzamide 
• 90763-44-3 C₁₇H₂₈N₄O₄S 

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.